Innovista specialty products from the house of Innovista Consulting. Brands that have been built with enthusiasm and knowledge and understanding of the the Livestock customer!
A transgenic crop plant contains a gene or genes which have been artificially inserted, instead of the plant acquiring them through pollination. The inserted gene sequence (known as the transgene) may come from another unrelated plant, or from a completely different species: for example, transgenic Bt corn, which produces its own insecticide, contains a gene from a bacterium. Plants containing transgenes are often called genetically modified or GM crops.
What is the need of transgenic plants?
A plant breeder tries to assemble a combination of genes in a crop plant which will make it as useful and productive as possible. The desirable genes may provide features such as higher yield or improved quality, pest or disease resistance, or tolerance to heat, cold and drought. This powerful tool enables plant breeders to do what they have always done - generate more useful and productive crop varieties containing new combinations of genes - but this approach expands the possibilities beyond the limitations imposed by traditional cross pollination and selection techniques.
Isolation and Characterization of Thermostable Protease Producing Bacteria fr...IOSR Journals
This study is a search for potential thermostable protease producing strain. Among nine protease
producing strains screened from soap industry effluent, one was selected as promising thermostable protease
producer and identified as Bacillus subtilis. The activity of the protease produced by this organism is stable up
to 70ºC. The optimum yield was achieved after 48 hours of culture, at 65ºC with the pH 8.0. The maximum
protease activity was observed at 65ºC and at pH 8.0.
Innovista specialty products from the house of Innovista Consulting. Brands that have been built with enthusiasm and knowledge and understanding of the the Livestock customer!
A transgenic crop plant contains a gene or genes which have been artificially inserted, instead of the plant acquiring them through pollination. The inserted gene sequence (known as the transgene) may come from another unrelated plant, or from a completely different species: for example, transgenic Bt corn, which produces its own insecticide, contains a gene from a bacterium. Plants containing transgenes are often called genetically modified or GM crops.
What is the need of transgenic plants?
A plant breeder tries to assemble a combination of genes in a crop plant which will make it as useful and productive as possible. The desirable genes may provide features such as higher yield or improved quality, pest or disease resistance, or tolerance to heat, cold and drought. This powerful tool enables plant breeders to do what they have always done - generate more useful and productive crop varieties containing new combinations of genes - but this approach expands the possibilities beyond the limitations imposed by traditional cross pollination and selection techniques.
Isolation and Characterization of Thermostable Protease Producing Bacteria fr...IOSR Journals
This study is a search for potential thermostable protease producing strain. Among nine protease
producing strains screened from soap industry effluent, one was selected as promising thermostable protease
producer and identified as Bacillus subtilis. The activity of the protease produced by this organism is stable up
to 70ºC. The optimum yield was achieved after 48 hours of culture, at 65ºC with the pH 8.0. The maximum
protease activity was observed at 65ºC and at pH 8.0.
Recent Breakthroughs in Genetic EngineeringSamar Biswas
Genetically engineered immune cells are saving the lives of cancer patients.
Precise Gene Editing in Plants.
DNA-editing breakthrough could fix 'broken genes' in the brain, delay ageing and cure incurable diseases
The Genetic engineering could slow aging, reverse blindness.
The genetic engineering that could change humanity.
Chinese researchers have genetically modified a human embryo.
Tubulin in molecular biology can refer either to the tubulin protein superfamily of globular proteins, or one of the member proteins of that superfamily. α- and β-tubulins polymerize into microtubules, a major component of the eukaryotic cytoskeleton. Microtubules function in many essential cellular processes, including mitosis. Tubulin-binding drugs kill cancerous cells by inhibiting microtubule dynamics, which are required for DNA segregation and therefore cell division. In eukaryotes there are six members of the tubulin superfamily, although not all are present in all species (see below). Both α and β tubulins have a mass of around 50 kDa and are thus in a similar range compared to actin with ~42 kDa. In contrast, tubulin polymers (microtubules) tend to be much bigger than actin filaments due to their cylindrical nature. Tubulin was long thought to be specific to eukaryotes. More recently, however, several prokaryotic proteins have been shown to be related to tubulin.
Anti-Epsilon Tubulin -http://www.stjohnslabs.com/epsilon-tubulin-antibody-2
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Plant Genetic engineering ,Basic steps ,Advantages and disadvantagesTessaRaju
plant genetic engineering,first genetically engineered crop plant,first genetically engineered foods,genome editing,uses of GE,transgenic plants,basic process of plant genetic enginering,advantages and disadvantages of genetic engineering.
Involved in autophagic vesicle formation. Conjugation with ATG12, through a ubiquitin-like conjugating system involving ATG7 as an E1-like activating enzyme and ATG10 as an E2-like conjugating enzyme, is essential for its function. The ATG12-ATG5 conjugate acts as an E3-like enzyme which is required for lipidation of ATG8 family proteins and their association to the vesicle membranes. Involved in mitochondrial quality control after oxidative damage, and in subsequent cellular longevity. The ATG12-ATG5 conjugate also negatively regulates the innate antiviral immune response by blocking the type I IFN production pathway through direct association with RARRES3 and MAVS. Also plays a role in translation or delivery of incoming viral RNA to the translation apparatus.
Anti-ATG5 - http://www.stjohnslabs.com/anti-atg5-antibody-p-104935?filter_name=STJ98903
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
Anti-α skeletal muscle actin -http://www.stjohnslabs.com/a-skeletal-muscle-actin-antibody-p-98686
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Biotechnological approaches for crop improvementShafqat Farooq
What is crop breeding?
Modifying, tailoring, and/or engineering plants
making them more suitable for humans
Modification means converting (e.g.):
a. Tall height to short height,
b. Late maturing to early maturing,
c. Disease susceptible to disease resistant,
d. Low yielding to high yielding,
e. Stress susceptible to stress tolerant
f. Low food quality to high food quality
Alpha-fetoprotein (AFP, α-fetoprotein; also sometimes called alpha-1-fetoprotein, alpha-fetoglobulin, or alpha fetal protein) is a protein that in humans is encoded by the AFP gene. The AFP gene is located on the q arm of chromosome 4 (4q25). AFP is a major plasma protein produced by the yolk sac and the liver during fetal development. It is thought to be the fetal form of serum albumin. AFP binds to copper, nickel, fatty acids and bilirubin[6] and is found in monomeric, dimeric and trimeric forms.
Anti-AFP alpha 1 Fetoprotein -http://www.stjohnslabs.com/afp-alpha-1-fetoprotein-antibody
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Biotechnology - Plant Biotechnology (Transgenic plants, Herbicide Resistant Plants, Glyphosate Tolerant Plants, Sulphonylurea Tolerant Plants, Atrazine Tolerant Plants, Phosphinothricin Tolerant Plants, Bromoxynil Tolerant Plants, Insect Resistant Plants, Animal Cells, Plant Cells, Tissue Cultures, Viruses, Prokaryotes)
Plant biotechnology is a precise process in which scientific techniques are used to develop molecular and cellular based technologies to improve plant productivity, quality and health; to improve the quality of plant products; or to prevent, reduce or eliminate constraints to plant productivity caused by diseases, pest organisms and environmental stresses. It can be defined as human intervention on plant material by means of technological instruments in order to produce permanent effects, and includes genetic engineering and gene manipulation to obtain transgenic plants.
See more
https://goo.gl/Tf0VTG
https://goo.gl/DySPuV
https://goo.gl/cncY7m
Contact us
Niir Project Consultancy Services
106-E, Kamla Nagar, Opp. Spark Mall,
New Delhi-110007, India.
Email: npcs.ei@gmail.com , info@entrepreneurindia.co
Tel: +91-11-23843955, 23845654, 23845886, 8800733955
Mobile: +91-9811043595
Website: www.entrepreneurindia.co , www.niir.org
Tags
Plant Biotechnology, Biotechnology Industry in India, Opportunities in Biotechnology and Business, Commercialization of Plant Tissue Culture in India, Agricultural Biotechnology, Biotechnology Industry in India, Biotechnology in India, Plant Biotech, Plant Tissue Culture, Plant Biotechnology and Agriculture, Plant Biology & Plant Biotechnology, Profitable Biotechnology Business Ideas, Small Business Ideas in Plant Biotechnology Industry, How to Start Small Scale Plant Biotech Industry in India, Start Tissue Culture Biotechnology, Plant Biotechnology Ideas for Small Business, Plant Biotechnology Business Plan, Plant Biotechnology Ideas, Plant Biotechnology Startups in India, Organisms of Biotechnology, Animal Cells, Plant Cells, Transgenic Plants, Herbicide Resistant Plants, Glyphosate Tolerant Plants, Sulphonylurea Tolerant Plants, Atrazine Tolerant Plants, Phosphinothricin Tolerant Plants, Bromoxynil Tolerant Plants, Insect Resistant Plants, Transgenic Plants With Cowpea Trypsin Inhibitor, Transgenic Plants With Viral Coat Protein, Transgenic Plants With Viral Nucleoprotein, Transgenic Plants With Viral SAT RNA, Transgenic Plants With Antisense RNA, Transgenic Plants Resistant to Fungi and Bacteria, Transgenic Plants With Improved Storage Proteins, Stress Tolerant Plants, Cold Tolerant Plants, Drought Tolerant Plants, Pharmaceutical Compounds, Biodegradable Plastics, Biological Nitrogen Fixations, Non-Symbiotic Nitrogen Fixation, Non-Symbiotic Nitrogen Fixation, Nif-Genes of Azotobacter, Nif-Genes of Anabaena, Legume Nodulin Genes, Transfer of Nif Genes to Yeasts, Transfer of Nif-Genes to Plants, Transfer of Hup Genes
TRANSGENIC CROPS CHALLENGES AND PROSPECTS
Transgenic Technology : Transform gene from any source.
Eg: animals, bacteria, virus etc
Traditional Breeding : Move genes only between members of a particular genus of plants.
Take multiple growing seasons to develop and test a new variety.
Lot of man power
Limited possibility of improved traits.
this presentation deals with Molecular Ph(f)arming, and bio-safety issues related to it. This was presented by me in credit seminar in the division of Agricultural physics, IARI, New Delhi.
the sources used are duly acknowledged in the figures and slides.
ATP-dependent RNA helicase which is a subunit of the eIF4F complex involved in cap recognition and is required for mRNA binding to ribosome. In the current model of translation initiation, eIF4A unwinds RNA secondary structures in the 5'-UTR of mRNAs which is necessary to allow efficient binding of the small ribosomal subunit, and subsequent scanning for the initiator codon. / ATP + H2O = ADP + phosphate.
Anti-eIF4A1-http://www.stjohnslabs.com/eif4a1-antibody-p-98673
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Efficacy of insecticides against citrus psylla diaphorina citri kuwayama in f...Muhammad Qasim
The experiments were conducted in a citrus orchard to check the efficacy of insecticides against citrus psylla, and mortality was observed after three days, seven days and then after one month. Four insecticides, Polytrin-C, Talstar, Bifenthrin and Imidacloprid applied, had an almost equal effect on the population reduction of citrus psylla on all citrus plants. The trial was laid out in randomized complete block design (RCBD) having five treatments with three replications in a citrus orchard, after three days of spray showed percentage control as 96.91%, 94.33%, 93.83% and 93.06% of following insecticides Polytrin- C, Imidacloprid, Bifenthrin and Actara, respectively, calculated by Minitab 15. Psylla adults were exposed to different concentrations (500, 400, 300, 200 and 100 ppm) of Imidacloprid and Bifenthrin, and two controlled conditions (with leaves and without leaves). Both Imidacloprid and Bifenthrin insecticides proved to be the most effective against D. citri with lethal times (LT50s) of 4 and 5 hours, respectively, at a concentration of 500 ppm, calculated from probability test with Minitab-15
The Effect of Dried Leaves Extract of Hyptis suaveolens on Various Stages of ...iosrjce
IOSR Journal of Pharmacy and Biological Sciences(IOSR-JPBS) is a double blind peer reviewed International Journal that provides rapid publication (within a month) of articles in all areas of Pharmacy and Biological Science. The journal welcomes publications of high quality papers on theoretical developments and practical applications in Pharmacy and Biological Science. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
Recent Breakthroughs in Genetic EngineeringSamar Biswas
Genetically engineered immune cells are saving the lives of cancer patients.
Precise Gene Editing in Plants.
DNA-editing breakthrough could fix 'broken genes' in the brain, delay ageing and cure incurable diseases
The Genetic engineering could slow aging, reverse blindness.
The genetic engineering that could change humanity.
Chinese researchers have genetically modified a human embryo.
Tubulin in molecular biology can refer either to the tubulin protein superfamily of globular proteins, or one of the member proteins of that superfamily. α- and β-tubulins polymerize into microtubules, a major component of the eukaryotic cytoskeleton. Microtubules function in many essential cellular processes, including mitosis. Tubulin-binding drugs kill cancerous cells by inhibiting microtubule dynamics, which are required for DNA segregation and therefore cell division. In eukaryotes there are six members of the tubulin superfamily, although not all are present in all species (see below). Both α and β tubulins have a mass of around 50 kDa and are thus in a similar range compared to actin with ~42 kDa. In contrast, tubulin polymers (microtubules) tend to be much bigger than actin filaments due to their cylindrical nature. Tubulin was long thought to be specific to eukaryotes. More recently, however, several prokaryotic proteins have been shown to be related to tubulin.
Anti-Epsilon Tubulin -http://www.stjohnslabs.com/epsilon-tubulin-antibody-2
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Plant Genetic engineering ,Basic steps ,Advantages and disadvantagesTessaRaju
plant genetic engineering,first genetically engineered crop plant,first genetically engineered foods,genome editing,uses of GE,transgenic plants,basic process of plant genetic enginering,advantages and disadvantages of genetic engineering.
Involved in autophagic vesicle formation. Conjugation with ATG12, through a ubiquitin-like conjugating system involving ATG7 as an E1-like activating enzyme and ATG10 as an E2-like conjugating enzyme, is essential for its function. The ATG12-ATG5 conjugate acts as an E3-like enzyme which is required for lipidation of ATG8 family proteins and their association to the vesicle membranes. Involved in mitochondrial quality control after oxidative damage, and in subsequent cellular longevity. The ATG12-ATG5 conjugate also negatively regulates the innate antiviral immune response by blocking the type I IFN production pathway through direct association with RARRES3 and MAVS. Also plays a role in translation or delivery of incoming viral RNA to the translation apparatus.
Anti-ATG5 - http://www.stjohnslabs.com/anti-atg5-antibody-p-104935?filter_name=STJ98903
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.
Anti-α skeletal muscle actin -http://www.stjohnslabs.com/a-skeletal-muscle-actin-antibody-p-98686
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Biotechnological approaches for crop improvementShafqat Farooq
What is crop breeding?
Modifying, tailoring, and/or engineering plants
making them more suitable for humans
Modification means converting (e.g.):
a. Tall height to short height,
b. Late maturing to early maturing,
c. Disease susceptible to disease resistant,
d. Low yielding to high yielding,
e. Stress susceptible to stress tolerant
f. Low food quality to high food quality
Alpha-fetoprotein (AFP, α-fetoprotein; also sometimes called alpha-1-fetoprotein, alpha-fetoglobulin, or alpha fetal protein) is a protein that in humans is encoded by the AFP gene. The AFP gene is located on the q arm of chromosome 4 (4q25). AFP is a major plasma protein produced by the yolk sac and the liver during fetal development. It is thought to be the fetal form of serum albumin. AFP binds to copper, nickel, fatty acids and bilirubin[6] and is found in monomeric, dimeric and trimeric forms.
Anti-AFP alpha 1 Fetoprotein -http://www.stjohnslabs.com/afp-alpha-1-fetoprotein-antibody
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Biotechnology - Plant Biotechnology (Transgenic plants, Herbicide Resistant Plants, Glyphosate Tolerant Plants, Sulphonylurea Tolerant Plants, Atrazine Tolerant Plants, Phosphinothricin Tolerant Plants, Bromoxynil Tolerant Plants, Insect Resistant Plants, Animal Cells, Plant Cells, Tissue Cultures, Viruses, Prokaryotes)
Plant biotechnology is a precise process in which scientific techniques are used to develop molecular and cellular based technologies to improve plant productivity, quality and health; to improve the quality of plant products; or to prevent, reduce or eliminate constraints to plant productivity caused by diseases, pest organisms and environmental stresses. It can be defined as human intervention on plant material by means of technological instruments in order to produce permanent effects, and includes genetic engineering and gene manipulation to obtain transgenic plants.
See more
https://goo.gl/Tf0VTG
https://goo.gl/DySPuV
https://goo.gl/cncY7m
Contact us
Niir Project Consultancy Services
106-E, Kamla Nagar, Opp. Spark Mall,
New Delhi-110007, India.
Email: npcs.ei@gmail.com , info@entrepreneurindia.co
Tel: +91-11-23843955, 23845654, 23845886, 8800733955
Mobile: +91-9811043595
Website: www.entrepreneurindia.co , www.niir.org
Tags
Plant Biotechnology, Biotechnology Industry in India, Opportunities in Biotechnology and Business, Commercialization of Plant Tissue Culture in India, Agricultural Biotechnology, Biotechnology Industry in India, Biotechnology in India, Plant Biotech, Plant Tissue Culture, Plant Biotechnology and Agriculture, Plant Biology & Plant Biotechnology, Profitable Biotechnology Business Ideas, Small Business Ideas in Plant Biotechnology Industry, How to Start Small Scale Plant Biotech Industry in India, Start Tissue Culture Biotechnology, Plant Biotechnology Ideas for Small Business, Plant Biotechnology Business Plan, Plant Biotechnology Ideas, Plant Biotechnology Startups in India, Organisms of Biotechnology, Animal Cells, Plant Cells, Transgenic Plants, Herbicide Resistant Plants, Glyphosate Tolerant Plants, Sulphonylurea Tolerant Plants, Atrazine Tolerant Plants, Phosphinothricin Tolerant Plants, Bromoxynil Tolerant Plants, Insect Resistant Plants, Transgenic Plants With Cowpea Trypsin Inhibitor, Transgenic Plants With Viral Coat Protein, Transgenic Plants With Viral Nucleoprotein, Transgenic Plants With Viral SAT RNA, Transgenic Plants With Antisense RNA, Transgenic Plants Resistant to Fungi and Bacteria, Transgenic Plants With Improved Storage Proteins, Stress Tolerant Plants, Cold Tolerant Plants, Drought Tolerant Plants, Pharmaceutical Compounds, Biodegradable Plastics, Biological Nitrogen Fixations, Non-Symbiotic Nitrogen Fixation, Non-Symbiotic Nitrogen Fixation, Nif-Genes of Azotobacter, Nif-Genes of Anabaena, Legume Nodulin Genes, Transfer of Nif Genes to Yeasts, Transfer of Nif-Genes to Plants, Transfer of Hup Genes
TRANSGENIC CROPS CHALLENGES AND PROSPECTS
Transgenic Technology : Transform gene from any source.
Eg: animals, bacteria, virus etc
Traditional Breeding : Move genes only between members of a particular genus of plants.
Take multiple growing seasons to develop and test a new variety.
Lot of man power
Limited possibility of improved traits.
this presentation deals with Molecular Ph(f)arming, and bio-safety issues related to it. This was presented by me in credit seminar in the division of Agricultural physics, IARI, New Delhi.
the sources used are duly acknowledged in the figures and slides.
ATP-dependent RNA helicase which is a subunit of the eIF4F complex involved in cap recognition and is required for mRNA binding to ribosome. In the current model of translation initiation, eIF4A unwinds RNA secondary structures in the 5'-UTR of mRNAs which is necessary to allow efficient binding of the small ribosomal subunit, and subsequent scanning for the initiator codon. / ATP + H2O = ADP + phosphate.
Anti-eIF4A1-http://www.stjohnslabs.com/eif4a1-antibody-p-98673
Join our Antibody Validation Project - http://www.stjohnslabs.com/services/antibody-validation
Efficacy of insecticides against citrus psylla diaphorina citri kuwayama in f...Muhammad Qasim
The experiments were conducted in a citrus orchard to check the efficacy of insecticides against citrus psylla, and mortality was observed after three days, seven days and then after one month. Four insecticides, Polytrin-C, Talstar, Bifenthrin and Imidacloprid applied, had an almost equal effect on the population reduction of citrus psylla on all citrus plants. The trial was laid out in randomized complete block design (RCBD) having five treatments with three replications in a citrus orchard, after three days of spray showed percentage control as 96.91%, 94.33%, 93.83% and 93.06% of following insecticides Polytrin- C, Imidacloprid, Bifenthrin and Actara, respectively, calculated by Minitab 15. Psylla adults were exposed to different concentrations (500, 400, 300, 200 and 100 ppm) of Imidacloprid and Bifenthrin, and two controlled conditions (with leaves and without leaves). Both Imidacloprid and Bifenthrin insecticides proved to be the most effective against D. citri with lethal times (LT50s) of 4 and 5 hours, respectively, at a concentration of 500 ppm, calculated from probability test with Minitab-15
The Effect of Dried Leaves Extract of Hyptis suaveolens on Various Stages of ...iosrjce
IOSR Journal of Pharmacy and Biological Sciences(IOSR-JPBS) is a double blind peer reviewed International Journal that provides rapid publication (within a month) of articles in all areas of Pharmacy and Biological Science. The journal welcomes publications of high quality papers on theoretical developments and practical applications in Pharmacy and Biological Science. Original research papers, state-of-the-art reviews, and high quality technical notes are invited for publications.
Toxicity of Ocimum gratissimum leaf extract on the developmental stages of ...researchanimalsciences
The effect of some plant extract on the developmental stages of mosquito
species was conducted using
Anopheles gambiae
,
Culex quinquefasciatus
and
Aedes aegypti
at the first instar, second instar, third instar, fourth instar, pupae and
adult. The plant used was scentleaf (
Ocimum gratissimum
). Soxhlet apparatus was
used to extract each pulverized plant part using petroleum ether solvent. Plant
extract from the petroleum ether solvent was used to test their effects on the
developmental stages of each mosquito species. The result showed that the higher
the developmental stages, the lower the percentage of mortality. It was also
observed that as the time and concentration increases, the percentage of mortality
also increases. Generally, the result showed that
Anopheles gambiae
is more
susceptible in the extracts used followed by
Aedes aegypti
and then
Culex
quinquefasciatus
.
This is a lecture by Dr. Jerry McLaughlin about his research into extracts of pawpaw plants, annonaceous acetogenins, in vitro, in vivo, mechanism of action, and toxicity in mice.
MS medium supplemented with different
concentrations of auxins 2,4-dichloro-phenoxyacetic acid (2,4-D),
α-naphthalene acetic acid (NAA) and combination with kinetin
were studied to obtain a suitable protocol of callus initiation of
Trigonella foenum graecum. Callus was induced from hypocotyls
and cotyledons explants which were collected from the seedlings
of the mentioned plant. The explants were cultured in MS
medium supplemented with two auxins 2,4-D and NAA
separately with different concentrations (0.0 as control, 0.1, 0.5,
1.0, 2.0, 3.0, 4.0 and 5.0 mg/l). Concentration of kinetin (0.5 mg/l)
was used in combination with all concentrations of 2, 4-D and
NAA hormones. The callus was successfully induced in all
different concentrations of two mentioned auxins and
combinations of different concentrations of two auxins separately
with (0.5 mg/l) of kinetin. No callus formation was observed in
the absence of plant growth regulators. Hypocotyl explants of
T.foenum- graecum were much better in inducing callus than
cotyledons explants. Combinations of NAA+Kin and 2,4-D+Kin
were found to be more effective for inducing callus from
hypocotyls explants compared to 2,4-D and NAA alone, at the
same time callus induced by 2,4-D using cotyledons explants
gave the best results compared to the other hormone. Among the
different concentrations of auxin and combinations with kinetin
,the highest mean of callusing index from hypocotyls segments
was (3.50±0.15) with 100% 0f callusing in sixth week by 4.0 mg/l
NAA+ 0.5mg/l Kin. In the case of callus induction from
cotyledons segments the highest mean of callusing index
(2.41±0.18) with 100% of callusing in sixth week was observed by
1.0 mg/l 2, 4-D
ANTIOXIDANT AND ANTIMICROBIAL ACTIVITIES OF ALGERIAN POPULUS NIGRA L. BUDS EX...bioejjournal
In organic extracts, tanins, flavonoïds, coumarins, alkaloids and terpenoïds were the principals secondary
metabolites identified from the flower buds of black poplar. Antibacterial and antifungal activities of
extracts were tested using agar-well diffusion method and micro-well determination of MIC assay against
eleven bacteria and two Candida species. It was found that extracts of black poplar buds exhibit
antibacterial and anticandidal activities with agar disk diffusion (7 to 43mm) and MIC methods (MIC=
90.33 µg/ml against several strains of bacteria and MIC=45.16 µg/ml against Candida albicans). The
antioxidant effect of hydroalcoholic extract was evaluated using DPPH and FRAP assays. It was showed
good and similar activity than ascorbic acid and BHA by DPPH method: IC50= 220µg/mL for
hydroethanol extract.
ANTIOXIDANT AND ANTIMICROBIAL ACTIVITIES OF ALGERIAN POPULUS NIGRA L. BUDS EX...bioejjournal
This study is part of a goal to investigate chemical composition, antibacterial, antifungal and antioxidant
activities of the flower buds extracts from the Algerian Polulus nigra L., which were collected from Djarifet
- mansourah at Tlemcen city in the West Northern of Algeria.
In organic extracts, tanins, flavonoïds, coumarins, alkaloids and terpenoïds were the principals secondary
metabolites identified from the flower buds of black poplar. Antibacterial and antifungal activities of
extracts were tested using agar-well diffusion method and micro-well determination of MIC assay against
eleven bacteria and two Candida species. It was found that extracts of black poplar buds exhibit
antibacterial and anticandidal activities with agar disk diffusion (7 to 43mm) and MIC methods (MIC=
90.33 µg/ml against several strains of bacteria and MIC=45.16 µg/ml against Candida albicans). The
antioxidant effect of hydroalcoholic extract was evaluated using DPPH and FRAP assays. It was showed
good and similar activity than ascorbic acid and BHA by DPPH method: IC50= 220µg/mL for
hydroethanol extract.
ANTIOXIDANT AND ANTIMICROBIAL ACTIVITIES OF ALGERIAN POPULUS NIGRA L. BUDS EX...bioejjournal
This study is part of a goal to investigate chemical composition, antibacterial, antifungal and antioxidant
activities of the flower buds extracts from the Algerian Polulus nigra L., which were collected from Djarifet
- mansourah at Tlemcen city in the West Northern of Algeria.
In organic extracts, tanins, flavonoïds, coumarins, alkaloids and terpenoïds were the principals secondary
metabolites identified from the flower buds of black poplar. Antibacterial and antifungal activities of
extracts were tested using agar-well diffusion method and micro-well determination of MIC assay against
eleven bacteria and two Candida species. It was found that extracts of black poplar buds exhibit
antibacterial and anticandidal activities with agar disk diffusion (7 to 43mm) and MIC methods (MIC=
90.33 µg/ml against several strains of bacteria and MIC=45.16 µg/ml against Candida albicans). The
antioxidant effect of hydroalcoholic extract was evaluated using DPPH and FRAP assays. It was showed
good and similar activity than ascorbic acid and BHA by DPPH method: IC50= 220µg/mL for
hydroethanol extract.
ANTIOXIDANT AND ANTIMICROBIAL ACTIVITIES OF ALGERIAN POPULUS NIGRA L. BUDS EX...bioejjournal
This study is part of a goal to investigate chemical composition, antibacterial, antifungal and antioxidant
activities of the flower buds extracts from the Algerian Polulus nigra L., which were collected from Djarifet
- mansourah at Tlemcen city in the West Northern of Algeria.
In organic extracts, tanins, flavonoïds, coumarins, alkaloids and terpenoïds were the principals secondary
metabolites identified from the flower buds of black poplar. Antibacterial and antifungal activities of
extracts were tested using agar-well diffusion method and micro-well determination of MIC assay against
eleven bacteria and two Candida species. It was found that extracts of black poplar buds exhibit
antibacterial and anticandidal activities with agar disk diffusion (7 to 43mm) and MIC methods (MIC=
90.33 μg/ml against several strains of bacteria and MIC=45.16 μg/ml against Candida albicans). The
antioxidant effect of hydroalcoholic extract was evaluated using DPPH and FRAP assays. It was showed
good and similar activity than ascorbic acid and BHA by DPPH method: IC50= 220μg/mL for
hydroethanol extract.
Antioxidant and Antimicrobial Activities Of Algerian Populus Nigra L. Buds Ex...bioejjournal
This study is part of a goal to investigate chemical composition, antibacterial, antifungal and antioxidant activities of the flower buds extracts from the Algerian Polulus nigra L., which were collected from Djarifet - mansourah at Tlemcen city in the West Northern of Algeria. In organic extracts, tanins, flavonoïds, coumarins, alkaloids and terpenoïds were the principals secondary metabolites identified from the flower buds of black poplar. Antibacterial and antifungal activities of
extracts were tested using agar-well diffusion method and micro-well determination of MIC assay against
eleven bacteria and two Candida species. It was found that extracts of black poplar buds exhibit
antibacterial and anticandidal activities with agar disk diffusion (7 to 43mm) and MIC methods (MIC=
90.33 µg/ml against several strains of bacteria and MIC=45.16 µg/ml against Candida albicans). The
antioxidant effect of hydroalcoholic extract was evaluated using DPPH and FRAP assays. It was showed good and similar activity than ascorbic acid and BHA by DPPH method: IC50= 220µg/mL for hydroethanol extract.
ANTIOXIDANT AND ANTIMICROBIAL ACTIVITIES OF ALGERIAN POPULUS NIGRA L. BUDS EX...bioejjournal
his study is part of a goal to investigate chemical composition, antibacterial, antifungal and antioxidant activities of the flower buds extracts from the Algerian Polulus nigra L., which were collected from Djarifet - mansourah at Tlemcen city in the West Northern of Algeria. In organic extracts, tanins, flavonoïds, coumarins, alkaloids and terpenoïds were the principals secondary metabolites identified from the flower buds of black poplar. Antibacterial and antifungal activities of extracts were tested using agar-well diffusion method and micro-well determination of MIC assay against eleven bacteria and two Candida species. It was found that extracts of black poplar buds exhibit antibacterial and anticandidal activities with agar disk diffusion (7 to 43mm) and MIC methods (MIC= 90.33 µg/ml against several strains of bacteria and MIC=45.16 µg/ml against Candida albicans). The antioxidant effect of hydroalcoholic extract was evaluated using DPPH and FRAP assays. It was showed good and similar activity than ascorbic acid and BHA by DPPH method: IC50= 220µg/mL for hydroethanol extract.
This is a portion of the talk given at the Certified Horticultural Retailer meetings across Alabama. This provides some more research-based insecticide updates compared to the earlier uploaded talk. Both organic and conventional insecticides have been discussed. Extension resources are mentioned at the end of the slide show. For feedback, email bugdoctor@auburn.edu. Join me on Facebook - look for ALABAMA VEGETABLE IPM.
SAP Sapphire 2024 - ASUG301 building better apps with SAP Fiori.pdfPeter Spielvogel
Building better applications for business users with SAP Fiori.
• What is SAP Fiori and why it matters to you
• How a better user experience drives measurable business benefits
• How to get started with SAP Fiori today
• How SAP Fiori elements accelerates application development
• How SAP Build Code includes SAP Fiori tools and other generative artificial intelligence capabilities
• How SAP Fiori paves the way for using AI in SAP apps
DevOps and Testing slides at DASA ConnectKari Kakkonen
My and Rik Marselis slides at 30.5.2024 DASA Connect conference. We discuss about what is testing, then what is agile testing and finally what is Testing in DevOps. Finally we had lovely workshop with the participants trying to find out different ways to think about quality and testing in different parts of the DevOps infinity loop.
Threats to mobile devices are more prevalent and increasing in scope and complexity. Users of mobile devices desire to take full advantage of the features
available on those devices, but many of the features provide convenience and capability but sacrifice security. This best practices guide outlines steps the users can take to better protect personal devices and information.
Dr. Sean Tan, Head of Data Science, Changi Airport Group
Discover how Changi Airport Group (CAG) leverages graph technologies and generative AI to revolutionize their search capabilities. This session delves into the unique search needs of CAG’s diverse passengers and customers, showcasing how graph data structures enhance the accuracy and relevance of AI-generated search results, mitigating the risk of “hallucinations” and improving the overall customer journey.
GraphSummit Singapore | The Future of Agility: Supercharging Digital Transfor...Neo4j
Leonard Jayamohan, Partner & Generative AI Lead, Deloitte
This keynote will reveal how Deloitte leverages Neo4j’s graph power for groundbreaking digital twin solutions, achieving a staggering 100x performance boost. Discover the essential role knowledge graphs play in successful generative AI implementations. Plus, get an exclusive look at an innovative Neo4j + Generative AI solution Deloitte is developing in-house.
GraphRAG is All You need? LLM & Knowledge GraphGuy Korland
Guy Korland, CEO and Co-founder of FalkorDB, will review two articles on the integration of language models with knowledge graphs.
1. Unifying Large Language Models and Knowledge Graphs: A Roadmap.
https://arxiv.org/abs/2306.08302
2. Microsoft Research's GraphRAG paper and a review paper on various uses of knowledge graphs:
https://www.microsoft.com/en-us/research/blog/graphrag-unlocking-llm-discovery-on-narrative-private-data/
Climate Impact of Software Testing at Nordic Testing DaysKari Kakkonen
My slides at Nordic Testing Days 6.6.2024
Climate impact / sustainability of software testing discussed on the talk. ICT and testing must carry their part of global responsibility to help with the climat warming. We can minimize the carbon footprint but we can also have a carbon handprint, a positive impact on the climate. Quality characteristics can be added with sustainability, and then measured continuously. Test environments can be used less, and in smaller scale and on demand. Test techniques can be used in optimizing or minimizing number of tests. Test automation can be used to speed up testing.
Removing Uninteresting Bytes in Software FuzzingAftab Hussain
Imagine a world where software fuzzing, the process of mutating bytes in test seeds to uncover hidden and erroneous program behaviors, becomes faster and more effective. A lot depends on the initial seeds, which can significantly dictate the trajectory of a fuzzing campaign, particularly in terms of how long it takes to uncover interesting behaviour in your code. We introduce DIAR, a technique designed to speedup fuzzing campaigns by pinpointing and eliminating those uninteresting bytes in the seeds. Picture this: instead of wasting valuable resources on meaningless mutations in large, bloated seeds, DIAR removes the unnecessary bytes, streamlining the entire process.
In this work, we equipped AFL, a popular fuzzer, with DIAR and examined two critical Linux libraries -- Libxml's xmllint, a tool for parsing xml documents, and Binutil's readelf, an essential debugging and security analysis command-line tool used to display detailed information about ELF (Executable and Linkable Format). Our preliminary results show that AFL+DIAR does not only discover new paths more quickly but also achieves higher coverage overall. This work thus showcases how starting with lean and optimized seeds can lead to faster, more comprehensive fuzzing campaigns -- and DIAR helps you find such seeds.
- These are slides of the talk given at IEEE International Conference on Software Testing Verification and Validation Workshop, ICSTW 2022.
Observability Concepts EVERY Developer Should Know -- DeveloperWeek Europe.pdfPaige Cruz
Monitoring and observability aren’t traditionally found in software curriculums and many of us cobble this knowledge together from whatever vendor or ecosystem we were first introduced to and whatever is a part of your current company’s observability stack.
While the dev and ops silo continues to crumble….many organizations still relegate monitoring & observability as the purview of ops, infra and SRE teams. This is a mistake - achieving a highly observable system requires collaboration up and down the stack.
I, a former op, would like to extend an invitation to all application developers to join the observability party will share these foundational concepts to build on:
Why You Should Replace Windows 11 with Nitrux Linux 3.5.0 for enhanced perfor...SOFTTECHHUB
The choice of an operating system plays a pivotal role in shaping our computing experience. For decades, Microsoft's Windows has dominated the market, offering a familiar and widely adopted platform for personal and professional use. However, as technological advancements continue to push the boundaries of innovation, alternative operating systems have emerged, challenging the status quo and offering users a fresh perspective on computing.
One such alternative that has garnered significant attention and acclaim is Nitrux Linux 3.5.0, a sleek, powerful, and user-friendly Linux distribution that promises to redefine the way we interact with our devices. With its focus on performance, security, and customization, Nitrux Linux presents a compelling case for those seeking to break free from the constraints of proprietary software and embrace the freedom and flexibility of open-source computing.
GDG Cloud Southlake #33: Boule & Rebala: Effective AppSec in SDLC using Deplo...James Anderson
Effective Application Security in Software Delivery lifecycle using Deployment Firewall and DBOM
The modern software delivery process (or the CI/CD process) includes many tools, distributed teams, open-source code, and cloud platforms. Constant focus on speed to release software to market, along with the traditional slow and manual security checks has caused gaps in continuous security as an important piece in the software supply chain. Today organizations feel more susceptible to external and internal cyber threats due to the vast attack surface in their applications supply chain and the lack of end-to-end governance and risk management.
The software team must secure its software delivery process to avoid vulnerability and security breaches. This needs to be achieved with existing tool chains and without extensive rework of the delivery processes. This talk will present strategies and techniques for providing visibility into the true risk of the existing vulnerabilities, preventing the introduction of security issues in the software, resolving vulnerabilities in production environments quickly, and capturing the deployment bill of materials (DBOM).
Speakers:
Bob Boule
Robert Boule is a technology enthusiast with PASSION for technology and making things work along with a knack for helping others understand how things work. He comes with around 20 years of solution engineering experience in application security, software continuous delivery, and SaaS platforms. He is known for his dynamic presentations in CI/CD and application security integrated in software delivery lifecycle.
Gopinath Rebala
Gopinath Rebala is the CTO of OpsMx, where he has overall responsibility for the machine learning and data processing architectures for Secure Software Delivery. Gopi also has a strong connection with our customers, leading design and architecture for strategic implementations. Gopi is a frequent speaker and well-known leader in continuous delivery and integrating security into software delivery.
UiPath Test Automation using UiPath Test Suite series, part 4DianaGray10
Welcome to UiPath Test Automation using UiPath Test Suite series part 4. In this session, we will cover Test Manager overview along with SAP heatmap.
The UiPath Test Manager overview with SAP heatmap webinar offers a concise yet comprehensive exploration of the role of a Test Manager within SAP environments, coupled with the utilization of heatmaps for effective testing strategies.
Participants will gain insights into the responsibilities, challenges, and best practices associated with test management in SAP projects. Additionally, the webinar delves into the significance of heatmaps as a visual aid for identifying testing priorities, areas of risk, and resource allocation within SAP landscapes. Through this session, attendees can expect to enhance their understanding of test management principles while learning practical approaches to optimize testing processes in SAP environments using heatmap visualization techniques
What will you get from this session?
1. Insights into SAP testing best practices
2. Heatmap utilization for testing
3. Optimization of testing processes
4. Demo
Topics covered:
Execution from the test manager
Orchestrator execution result
Defect reporting
SAP heatmap example with demo
Speaker:
Deepak Rai, Automation Practice Lead, Boundaryless Group and UiPath MVP
UiPath Test Automation using UiPath Test Suite series, part 5DianaGray10
Welcome to UiPath Test Automation using UiPath Test Suite series part 5. In this session, we will cover CI/CD with devops.
Topics covered:
CI/CD with in UiPath
End-to-end overview of CI/CD pipeline with Azure devops
Speaker:
Lyndsey Byblow, Test Suite Sales Engineer @ UiPath, Inc.
GraphSummit Singapore | The Art of the Possible with Graph - Q2 2024Neo4j
Neha Bajwa, Vice President of Product Marketing, Neo4j
Join us as we explore breakthrough innovations enabled by interconnected data and AI. Discover firsthand how organizations use relationships in data to uncover contextual insights and solve our most pressing challenges – from optimizing supply chains, detecting fraud, and improving customer experiences to accelerating drug discoveries.
4. GROWTH REGULATORS
Compounds which have a different action
from the conventional insecticides
They
a
INSE re also known
as “ I
CT G
R O W GR ”
REG
TH
U
LATO
R
5. “IGRs” CHARACTERISTICS
Interfere with the
metamorphosis and ecdysis
control mechanism.
Act on specific Arthropods
enzymes.
Give a long residual protection.
Act on juvenile forms of insects.
Can cause the adult females to
lay unviable eggs.
They don’t offer the knock
down effect.
6. ACTION MODE - CLASSIFICATION
CHITIN
SYNTHESIS
INHIBITORS
Synthetase enzyme =
responsible for the
chitin formation
process. IGRs
prevent its
polymerization.
Ex.: Flufenoxuron.
AGONISTS OF
ECDYSTEROIDS
JUVENILE
HORMONE AGONISTS
Imitate the insects natural
hormone ("ecdisônio"),
prematurely triggering the
process of change.
"Juvenoid" = Imitate the action
of the insects juvenile
hormone by interfering with
the skin changes.
Ex.: Tefubenoside,
Metoxifenoside.
Ex.: Piriproxifen,
Fenoxicarb, Metoprene.
7. POLYSACCHARIDES
Carbohydrates formed by the union of more
than ten monosaccharide molecules, forming
a polymer of monosaccharides
MONOSACCHARIDES
FRUCTOSE
BETA- GLUCOSE
Energy
Ex.: Starch, Glycogen
Structural
Ex.: Chitin, Cellulose
Unlike the mono-and disaccharides (glucose, galactose, fructose),
polysaccharides are insoluble in water and are well suited to the role of
nutritional reserves or storage.
9. FUNGUS - CELL WALL
mannoproteins
FUNCTIONS
ß (1,3)
Protection adverse
factors
ß (1,6) glucan
Permeability
barrier
ß (1,3) glucan
Plasma membrane
chitin
synthase
Cell shape
ergosterol
Interaction with the
external environment
Atlas of fungal Infections, Richard Diamond Ed. 1999 - Introduction to Medical Mycology. Merck and Co. 2001
10. FLUFENOXURON
Chemical group:
Benzoyl phenyl urea
Solubility in water: 0,0043 mg/l
(25º)
Acute oral DL50(rat):
> 3000 mg/kg (téc.)
85% eliminated in feces within
72 hours (rats)
Not irritanting
Classe III – OMS
11. LABORATORY RESULTS- FLUFENOXURON
Blattella germanica
Until 98 days:
5 mg/m²
M
O
R
T
A
L
I
T
Start with 8 adults (3 males/ 5
females, and 3 with ooteca), and
10 nymphs in 1º ínstar and 5 the
last ínstar.
10 mg/m²
Control
After 100 days:
Y%
New population with 7 adults (3
males/4 females, and 2 with
ooteca), and 7 nymphs in 1º ínstar
and 5 the last ínstar.
Area treated: 10% of the total area disponível.Obs.: Total area
with availability of food, shelter and water.
Food And Environment Protection Act 1985, Part III
12. ESTIMATED POPULATION IN 98 DAYS
Blattella germanica
Biological Characteristics
Domestic Species
Blattella germanica
Size
12 a 16 mm
Color
yellowish brown
Ootheca Deposition
not release
Number of eggs / ootheca
30-40
Number of ootheca
4-5
Number of Ecdysis
5-7
young period
2-3 months
longevity
1 year
eggs incubation
15-30 days
posture interval
45 days
Succession number
20 000
days to produce the first ootheca
17
98 days estimate
5369X 5 – 26.845
13. FIELD RESULTS - FLUFENOXURON
Blattella germanica
%
P
O
P
U
L
A
T
I
O
N
R
E
D
U
C
T
I
O
N
Inicial
on
populati
Index Infestation measured
with glue trap.
(captures per night)
Dose found in the treated surfaces
(chromatographic analysis - mg / m²):
Apart 01:
-
Apart 02: 6,33
Apart 03:
-
Apart 04: 4,53
Rate: 7,5 mg/m²
Food And Environment Protection Act 1985, Part III
Apart 05: 5,24
Apart 06: 3,65
14. FIELD RESULTS - FLUFENOXURON
Blattella germanica
Apart. 02
Nº
I
N
S
E
C
T
S
C
A
P
T
U
R
E
D
Food And Environment Protection Act 1985, Part III
ADULTS
NYMPHS
15. LABORATORY RESULTS – FLUFENOXUROM
Ctenocephalides felis
PUPAE
DEAD LARVAE
TREATMENT
RESULTS WITH
ADULTS - SECOND
STAGE (%)
Control
72,5
62
4
0,8 mg/m²
0,98
38
23
4,0 mg/m²
0
5
68
NUMBER
5 repetitions of 15 to 20 larvae of second ínstar
Flufenoxuron - control in
the development of the
second stage
16. LIFE CYCLE - FLEAS
Ctenocephalides felis
Adults
Pupa
Adult Flea
Eggs
Pupa
Animals
Larvae
Larvae
3º stage
Larvae
1º stage
Environment
Environment
Environment
Larvae
2º stage
LIFE CYCLE
Eggs
Cycle Time - 17 to 25 days
Approximately 3000 eggs
17. FIELD RESULTS - FLUFENOXURON
Ctenocephalides felis
Rate:
Eggs collected
Dead Larvae
15 mg/m²
METHODOLOGY
1)
Cat’s Cloth (40 cm²) jerky
and collected;
Alive Adults
2)
Count number of eggs;
Adults Control (%)
3)
Incubated eggs;
4)
Note the development of
eggs.
Alive Larvae
W
ks
ee
Control with 77 weeks
Food And Environment Protection Act 1985, Part III
18. FLUFENOXURON RECOMMENDATIONS - OMS
Cockroaches: Rate 0,3 g/L
“Due to its slow-acting insecticides are usually combined with faster
acting insectcides. This combination eliminates adults and prevents the
development of young forms”
Bed Bugs: Rate 0,3 g/L
“Studies have shown the bed bugs resistance to conventional
insecticides.The mixtures of Growth Regulators + Pyrethroids have
proven to be an effective control compared to infestations tolerant to
pyrethroids when it is used alone. "
Food And Environment Protection Act 1985, Part III
19. TENOPA® - ESPECIFICATIONS
Physical State:
opaque and
viscous liquid
Color: white
Oxidant:
considered
non oxidizing
Density: 1,028
Smell: Odeurless
Shelf stability
Good stability in:
20 a 28º C - 104 weeks / 728 days
Acid/Base: PH
7.2
29 a 37º C - 52 weeks / 364 days
20. INSTRUCTIONS FOR USE
PESTS
COMERCIAL
PRODUCT
(ml/ 10 L of water)
I.A.
CONCENTRATION
ALPHA-CIPERMETRIN
(%P/P)
I.A.
CONCENTRATION
FLUFENOXURON
(%P/P)
Cockroaches
50
0,015%
0,015%
Mosquitoes
67
0,020%
0,020%
Flies
67
0,020%
0,020%
Fleas
33
0,010%
0,010%
Ants
50
0,015%
0,015%
Triatomines
133
0,040%
0,040%
Ticks
80
0,024%
0,024%
Scorpions
170
0,050%
0,050%
Mealworm
150
0,045%
0,045%
Bed bug
170
0,050%
0,050%
Brown spider
170
0,050%
0,050%
21. LIFE CYCLE - COKROACHES
Periplaneta Americana
Males
Females
22. LABORATORY RESULTS
Tile surface - Blatella germanica
9
8
7
Minutes
6
5
Upper limit
KT50
4
Lower limit
K
IC N
QU TIO
AC
3
2
1
0
Check
Alfa-Cipermetrina 3%+
Flufenoxueom 3%
(TENOPA )
®
Source : Non Crop Laboratory = EEA BASF- Brazil, 2010
Alpha-Cypermethrin
Lambdacyalothrin
Deltamethrin
5%
2,5%
2,5%
23. LABORATORY RESULTS
Wood surface - Blatella germanica
100
90
K
IC N
QU TIO
AC
80
70
Minutes
60
Upper limit
50
KT50
40
Lower limit
30
20
10
0
Check
Alpha-Cypermethrin 3%+ Alpha-Cypermethrin
5%
Flufenoxueon 3%
(TENOPA )
®
Source : Non Crop Laboratory = EEA BASF- Brazil, 2010
Lambdacyalothrin
Deltamethrin
2,5%
2,5%
24. LABORATORY RESULTS
Blatella germanica
TILE SURFACE - tile surface
PRELIMINARY PROFILE
ACTIVE
INGREDIENT
CONC. Appl.
(g a.i./l) (Nº)
RATE
(10l of water)
Alphacypermethrin+
Flufenoxuron
30/30
1
50
1
25
1
25
1
EFFICACY
30 DAYS
EFFICACY
60 DAYS
EFFICACY
90 DAYS
10%
20%
EFFICACY
60 DAYS
EFFICACY
90 DAYS
100ml/200m²
Deltamethrin
EFFICACY
72 HOURS
50ml/200m²
Lambdacyalothrin
EFFICACY
48 HOURS
50ml/200m²
Alphacypermethrin
EFFICACY
24 HOURS
100ml/200m²
Subtitles
WOOD SURFACE
PRELIMINARY PROFILE - wooden surface
ACTIVE
INGREDIENT
CONC. Appl.
(g a.i./l) (Nº)
RATE
(10l of water)
Alphacypermethrin+
Flufenoxuron
30/30
1
50ml/200m²
Alphacypermethrin
50
1
50ml/200m²
Lambdacyalothrin
25
1
100ml/200m²
Deltamethrin
25
1
100ml/200m²
P&D Brasil
Source : Non Crop Laboratory = EEA BASF- Brazil, 2010
EFFICACY
24 HOURS
EFFICACY
48 HOURS
EFFICACY
72 HOURS
0
EFFICACY
30 DAYS
25. RESULTS – RESIDUAL EFFECT
Periplaneta / Blatella
Rate:
50 mL - 10 L of
water
Days
Ecolyzer
ANVISA Standard
26. RESULTS – KNOCK DOWN
Periplaneta / Blatella
Rate:
TIME
50 mL - 10 L of
water
Days
Ecolyzer
ANVISA Standard
KT 50 with confidence interval of 95%
Ex.: Periplaneta - time 24h - result 6,13 min – confidence interval = 4,49/8,35 min
34. 3 1
Single Insecticide = The first
in
on the market:
KNOCK DOWN + RESIDUAL + ACTION
in all the insects phases.
Versatility of the product = Broad spectrum of action
Pyrethroid + IGR = Residual Effecty longer
Active Formulation = For use in the Resistance Management.
Technical Advantage Formulation = To control
cockroaches and Bed Bugs
Differentiated Formulation "SC" = Odorless, water
based, solvent-free organic.
Low toxicity
BASF PRODUCT = DIFFERENTIATED PRODUCT