This is Maggie from Foregene(www.foreivd.com), a life science company focused on molecular biology.
We're founded by experts from Yale university, and Gene company with 20+ years experience in life science industry, and with 10+ years foundation in life science reagent, including DNA/RNA isolation kit, PCR/qPCR reagent, genotyping kit, IVD kit, PCR machines, and other consumables, etc.
In 2019, we launched out the covid-19 RT-PCR kit in 3 days at the pandemic break, and ranked the 1st producer for the test kits in Southwestern China.Besides, the life science reagent is also covered in 80%+ universities in China, and the large hospital labs.
Any questions, feel free to contact me.
Regards,
Maggie | Sales
Foregene Co., Ltd
www.foreivd.com
Mob:008615281067355
Foregene RNA isolation kits for animal,cell, plant, and virus.
Main features:
Complete total RNA extraction in 11 minutes
Safe, non-toxic, environmental friendly
Room temperature operation
No DNase added, no effect on subsequent experiments
maggie@foregene.com
Foregene's detection solution to covid 19Maggie Ma
In response to the Covid-19, Foregene developes the RT-PCR kit within 3 days.Based on Direct PCR tech, test centers needn't buy extra nucleic acid extraction kit and machine, just do PCR directly.It's so economical way. This kit is CE certificated, and welcomed by 10+ countries with stable quality and competitive prices.
The variant nucleic acid detection kit for Brazil, UK,India,and South Africa is also available with high specificity and sensitivity.
Are you a medical device importer?
Welcome your enquiry. E-mail:maggie@foregene.com
Available now from Accuscience Ireland. Many topical and geographically important tests have been developed to allow producers and companion animal owners/veterinarians to screen animals quickly and with the high sensitivity of qPCR. Within the veterinary and agricultural range of pathogens detection kits are diseases and infections which can have significanteconomic impact. If your test is not available contact us to enquire about getting a custom kit made for you.
The Delta Seek detection kits utilise the sensitivity and speed of qPCR to get the most accurate data as quickly as possible. Each kit is specifically designed by our bioinformatics team to ensure the broadest possible detection profile and detection of all clinically relevant strains and subtypes. All test kits are validated in house on multiple qPCR platforms to ensure cross platform functionality.
Foregene RNA isolation kits for animal,cell, plant, and virus.
Main features:
Complete total RNA extraction in 11 minutes
Safe, non-toxic, environmental friendly
Room temperature operation
No DNase added, no effect on subsequent experiments
maggie@foregene.com
Foregene's detection solution to covid 19Maggie Ma
In response to the Covid-19, Foregene developes the RT-PCR kit within 3 days.Based on Direct PCR tech, test centers needn't buy extra nucleic acid extraction kit and machine, just do PCR directly.It's so economical way. This kit is CE certificated, and welcomed by 10+ countries with stable quality and competitive prices.
The variant nucleic acid detection kit for Brazil, UK,India,and South Africa is also available with high specificity and sensitivity.
Are you a medical device importer?
Welcome your enquiry. E-mail:maggie@foregene.com
Available now from Accuscience Ireland. Many topical and geographically important tests have been developed to allow producers and companion animal owners/veterinarians to screen animals quickly and with the high sensitivity of qPCR. Within the veterinary and agricultural range of pathogens detection kits are diseases and infections which can have significanteconomic impact. If your test is not available contact us to enquire about getting a custom kit made for you.
The Delta Seek detection kits utilise the sensitivity and speed of qPCR to get the most accurate data as quickly as possible. Each kit is specifically designed by our bioinformatics team to ensure the broadest possible detection profile and detection of all clinically relevant strains and subtypes. All test kits are validated in house on multiple qPCR platforms to ensure cross platform functionality.
Advancing Microbiome Research: From challenging samples to insight with Confi...QIAGEN
Microbiome research encompasses sample types as diverse as the human gut, Antarctic soil, ocean water and acidic hot spring biofilms. These samples are challenging because they are difficult to lyse, with some microbes containing a tough extracellular matrix. Incomplete lysis of a microbial community results in an inaccurate representation of the microbial content of the sample. Additionally, PCR inhibitors present in these samples, especially humic acids, polysaccharides, polyphenolics, lipids and heavy metals result in inaccurate quantification of nucleic acids that may inhibit downstream applications such as qPCR and NGS.
As you know, Sample preparation is a relevant step to get the success in your research. For this reason, Canvax™ Extraction kits are designed for a reliable, easy and fast purification of high-quality and high-purity genomic DNA/RNA from a wide range of starting materials, like Blood, Buccal Swab, Buccal Saliva, Tissues, Cultured cells, Stool samples, Plant tissues, Soil samples, Bacteria, Yeast, Plasmid, PCR mixtures, Agarose gel slices or Serum.
Our breakthrough and proprietary technologies HigherPurity™, CleanEasy™ and WideUSE™ improves the most common Extraction methods conferring the obtained DNA and RNA a proven optimal performance for all downstream applications, such as PCR, qPCR, NGS, Cloning, STR Analysis or Gene Expression.
Automated Nucleic Acid Purification from Diverse Sample types using dedicated...QIAGEN
This webinar will focus on the automation of QIAGEN’s new line of DNA and RNA sample prep kits for the microbiome. We will show how automation on the QIAcube enables efficient and reliable use of these samples for sensitive downstream applications such as qPCR and NGS. In addition, you will learn how to successfully use the CLC Microbial Genomics Module for metagenome sequencing and identification of microbial composition and diversity.
Advancing Microbiome Research: From challenging samples to insight with Confi...QIAGEN
Microbiome research encompasses sample types as diverse as the human gut, Antarctic soil, ocean water and acidic hot spring biofilms. These samples are challenging because they are difficult to lyse, with some microbes containing a tough extracellular matrix. Incomplete lysis of a microbial community results in an inaccurate representation of the microbial content of the sample. Additionally, PCR inhibitors present in these samples, especially humic acids, polysaccharides, polyphenolics, lipids and heavy metals result in inaccurate quantification of nucleic acids that may inhibit downstream applications such as qPCR and NGS.
As you know, Sample preparation is a relevant step to get the success in your research. For this reason, Canvax™ Extraction kits are designed for a reliable, easy and fast purification of high-quality and high-purity genomic DNA/RNA from a wide range of starting materials, like Blood, Buccal Swab, Buccal Saliva, Tissues, Cultured cells, Stool samples, Plant tissues, Soil samples, Bacteria, Yeast, Plasmid, PCR mixtures, Agarose gel slices or Serum.
Our breakthrough and proprietary technologies HigherPurity™, CleanEasy™ and WideUSE™ improves the most common Extraction methods conferring the obtained DNA and RNA a proven optimal performance for all downstream applications, such as PCR, qPCR, NGS, Cloning, STR Analysis or Gene Expression.
Automated Nucleic Acid Purification from Diverse Sample types using dedicated...QIAGEN
This webinar will focus on the automation of QIAGEN’s new line of DNA and RNA sample prep kits for the microbiome. We will show how automation on the QIAcube enables efficient and reliable use of these samples for sensitive downstream applications such as qPCR and NGS. In addition, you will learn how to successfully use the CLC Microbial Genomics Module for metagenome sequencing and identification of microbial composition and diversity.
The technique of molecular biology like DNA isolation, RNA isolation, PCR, Western blot, RFLP, etc was developed with development in science. This presentation includes the method of DNA and RNA isolation and their Quantification techniques.
Some sample sources present special challenges in RNA isolation or contain substances that cause problems in RNA analysis. These guides to RNA isolation have tips for a whole range of sample types, including guidance on the best kits for each.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
3. • Foregene Co., Ltd is specialtized in the IVD kits and R&D reagents production and services, which is
integrated in R&D, production and marketing.
• Foregene currently has world’s leading Direct PCR technology platform, DNA-only silica membrane
technology platform, and LncRNA research one-stop technology service platform. The main products
include various IVD kits, nucleic acid purification reagents,PCR and Direct PCR reagents,Genotyping kits,
etc.
• The technology and product performance indicators used are all leading the world status, widely used in
basic research fields of life sciences, medicine, agriculture, pharmacy, environment, etc, welcomed by
hospitals, institutions, medical laboratories, etc.
Company Introduction
4. Key Figures
Team of 30 (PhD and master)
2500㎡ office building
600㎡ P2 laboratory
1200㎡ GMP workshop
2015 Sichuan Province "Thousand Talents Plan" entrepreneurial team
2018 Selected as the entrepreneurial team of Chengdu "Rongpiao Project"(funded by RMB 5
million)
5. Platforms
• With special technology, the nucleic acid needn’t be extracted,
just do PCR directly.
Direct PCR technology
platform
• The RNA-Only Column and DNA-Cleaning Column was adopted to
achieve rapid purification of genomic DNA without DNase, high-
quality total RNA can be isolated.
DNA-only silica membrane
technology platform
• Used in screening and identification, target identification,
functional research.
LncRNA research one-
stop technology service
platform
6. Product Series
Life science product Series Features
RNA Purification Quickly and efficiently extract high-purity and high-quality total RNA from various animal
tissues,cells, plants, and virus, etc.
DNA Purification Rapid extraction and purification of genomic DNA from animal, blood, bacteria,plant,mouse
tail,water,stool, etc.
PCR/RT-PCR Easily and efficiently synthesize high-quality first-strand cDNA,simple and fast operation of
PCR and RT-PCR
Direct PCR Directly use sample lysate as a template for PCR amplification, without separate extraction
of DNA, fast and high sensitivity. Such as animal tissue,mouth tail, zebra fish,blood,plant
leaf,plant seed,etc.
IVD kits SARS-CoV-2 Nucleic acid detection kits by multiplex fluorescent PCR method, for detection
of ORF1ab, N, E,S genes, flu A and B, etc.
Lab equipment and
consumables
PCR machine, real time PCR system, and more to come.
7. Product Catalogues
Plasmid DNA purification,DNA fragment purification and recovery, genomic DNA purification series
Series Product Name Descriptions Specifications
Catalogue
Number
Storage Conditions
Plasmid DNA purification
General plasmid mini-extraction kit
General Plasmid Mini Kit
Quickly purify high-quality plasmid DNA from transformed bacteria for
routine molecular biology experiments such as transformation and
enzyme digestion
50 Preps DE-01001
Short-term room temperature,
long-term 2-8℃
DNA fragment purification
and recovery
Gel Extraction Kit
Gel Extraction Kit
Quickly and efficiently recover 20bp-10kb DNA fragments from agarose
gel
50 Preps DE-02011
Short-term room temperature,
long-term 2-8℃
PCR Purification Kit
PCR Purification Kit
Quickly purify and obtain high-quality DNA fragments from the PCR
system; if you want to separate and obtain specific DNA fragments,
please choose a gel recovery kit
50 Preps DE-03011
Short-term room temperature,
long-term 2-8℃
Genomic DNA purification
series
Animal Tissue DNA Isolation Kit
Animal Tissue DNA Isolation Kit
Rapid extraction and purification of genomic DNA from multiple sources,
such as animal tissues, cells, etc.
50 Preps DE-05011
Protease 4℃,
other room temperature
Blood DNA Mini Kit(<1ml)
Blood DNA Mini Kit(<1ml) Quickly purify high-quality genomic DNA from anticoagulated blood (<1ml) 50 Preps DE-05111
Protease 4℃,
other room temperature
Blood DNA Midi Kit(1-5ml)
Blood DNA Midi Kit(1-5ml)
Quickly purify high-quality genomic DNA from anticoagulated blood (1-
5ml)
50 Preps DE-05121
Protease 4℃,
other room temperature
Mouse Tail DNA Mini Kit
Mouse Tail DNA Mini Kit
The world's fastest kit for extracting mouse tail genomic DNA, which can
extract high-quality genomic DNA from mouse tail within 1 hour
50 Preps DE-05211
Protease 4℃,
other room temperature
Bacterial DNA Isolation Kit
Bacterial DNA Isolation Kit
Quickly purify high-quality genomic DNA from bacteria in the logarithmic
growth phase
50 Preps DE-05311 Protease 4℃, Lysozyme -20℃
8. Product Catalogues
Plasmid DNA purification,DNA fragment purification and recovery, genomic DNA
purification series
Series Product Name Descriptions Specifications
Catalogue
Number
Storage Conditions
Genomic DNA purification
series
FFPE DNA Isolation Kit
FFPE DNA Isolation Kit
Quickly purify high-quality genomic DNA from paraffin-embedded
tissues such as paraffin sections and paraffin blocks
50 Preps DE-05411
Protease 4℃,
other room temperature
Soil DNA Isolation Kit
Soil DNA Isolation Kit
Quickly purify and obtain high-quality genomic DNA from various soil
sample microorganisms
50 Preps DE-05513 Protease 4℃, Lysozyme -20℃
Water DNA Isolation Kit
Water DNA Isolation Kit
Quickly purify high-quality genomic DNA from microorganisms in
various water samples
50 Preps DE-05613 Protease 4℃, Lysozyme -20℃
Stool DNA Isolation Kit
Stool DNA Isolation Kit
Quickly purify and obtain high-quality genomic DNA from various stool
samples
50 Preps DE-05713 Protease 4℃, Lysozyme -20℃
Buccal Swab(FTA Card)DNA
Isolation Kit
Buccal Swab(FTA Card)DNA
Isolation Kit
Quickly purify high-quality genomic DNA from buccal swab samples 50 Preps DE-05811
Protease 4℃,
other room temperature
Plant DNA Isolation Kit
Plant DNA Isolation Kit
Quickly purify and obtain high-quality genomic DNA from plant
samples (including polysaccharides and polyphenol plant samples)
50 Preps DE-06111
Protease 4℃,
other room temperature
Genomic DNA Micro Kit
Genomic DNA Micro Kit Quickly purify small samples to obtain high-quality genomic DNA 50 Preps DM-01011
Protease 4℃,
other room temperature
RNA purification series
Animal miRNA Isolation Kit
Animal miRNA Isolation Kit
Quickly and efficiently extract small RNA fragments of 20-200nt
miRNA, siRNA, snRNA from various animal tissues and cells
50 Preps RE-01011
Room temperature
200 Preps RE-01014
Serum(Plasma) miRNA Isolation Kit
Serum(Plasma) miRNA Isolation Kit
Fast and efficient separation and purification of miRNAs with a length
of less than 100 nt from human live animal serum and plasma
samples
50 Preps RE-01111
Room temperature
200 Preps RE-01114
9. Product Catalogues
Series Product Name Descriptions Specifications
Catalogue
Number
Storage Conditions
RNA purification
series
Viral RNA Isolation Kit
Viral RNA Isolation Kit
Rapidly isolate and purify viral RNA from samples such as plasma, serum,
cell-free body fluids and cell culture supernatants
50 Preps RE-02011
Room temperature
200 Preps RE-02014
Viral DNA&RNA Isolation Kit
Viral DNA&RNA Isolation Kit
Quickly isolate and purify virus DNA or RNA from samples such as
plasma, serum, cell-free body fluid and cell culture supernatant
50 Preps DR-01011
Room temperature
200 Preps DR-01013
Animal Total RNA Isolation Kit
Animal Total RNA Isolation Kit
Quickly and efficiently extract high-purity and high-quality total RNA from
various animal tissues
50 Preps RE-03011
Room temperature
200 Preps RE-03014
Cell Total RNA Isolation Kit
Cell Total RNA Isolation Kit
Highly purified and high-quality total RNA can be obtained from various
cultured cells in 11 minutes
50 Preps RE-03111
Room temperature
200 Preps RE-03113
Plant Total RNA Isolation Kit(Samples low in
polysaccharides and polyphenols)
Plant Total RNA Isolation Kit(Samples low in
polysaccharides and polyphenols)
Quickly extract high-quality total RNA from plant samples with low
polysaccharide and polyphenol content
50 Preps RE-05011
Room temperature
200 Preps RE-05014
Plant Total RNA Isolation Kit Plus(Samples high in
polysaccharides and polyphenols)
Plant Total RNA Isolation Kit Plus(Samples high in
polysaccharides and polyphenols)
Quickly extract high-quality total RNA from plant samples with high
content of polysaccharides and polyphenols
50 Preps RE-05021
Room temperature
200 Preps RE-05024
RNAlater(For RNA Stabilization)
RNAlater(For RNA Stabilization)
Fast fixation of newly taken animal sample tissues, inhibit RNase activity,
protect RNA from degradation
50ml RL-01011
Room temperature
RNase Eraser
RNase Eraser
Used in laboratories to remove RNase contamination on the solid surface,
especially in RNA manipulation laboratories.
100ml RC-01011
Room temperature
100ml×15 RC-01012
10. Product Catalogues
Series Product Name Descriptions Specifications
Catalogue
Number
Storage Conditions
MIX series
PCR Hero ™
PCR Hero ™
Ultra-efficient PCR reaction premix system, suitable for a variety of difficult to
amplify PCR templates
5ml PH-01013
-20℃
40ml PH-01015
PCR Hero ™(With Dye)
PCR Hero™(With Dye) High-efficiency PCR premix system
5ml PH-01013-B
-20℃
40ml PH-01015-B
2×High-efficiency PCR reaction
premix system
2×High-efficiency PCR reaction
premix systemPCR EasyTM
Efficient PCR reaction premix system, suitable for various difficult to amplify
PCR templates
1ml DP-20031
-20℃
3×1.7ml DP-20032
PCR EasyTM(with dye)
PCR EasyTM(with dye)
Efficient PCR reaction premix system, suitable for various difficult to amplify
PCR templates
3×1.7ml DP-20032-B
-20℃
50ml DP-20034-B
2×Rapid PCR reaction premix
system
2×Rapid PCR reaction premix
system
2× PCR Mix
Fast PCR reaction premix system
1ml DP-20041
-20℃
3×1.7ml DP-20042
Real Time PCR kit
Real Time PCR EasyTM-SYBR
Green I
Using SYBR Green I for Real Time PCR amplification reaction can greatly
improve product specificity and reaction sensitivity, and the fluorescence
intensity is 3-5 times that of similar products
500 ×20μl rxns QP-01012
-20℃
2000 ×20μl rxns QP-01014
Real Time PCR kit-Taqman
Real Time PCR EasyTM-
Taqman
Use specific fluorescent probes for Real Time PCR amplification reaction,
which can greatly improve product specificity and reaction sensitivity
500 ×20μl rxns QP-01022
-20℃
2000 ×20μl rxns QP-01024
11. Product Catalogues
Series Product Name Descriptions Specifications
Catalogue
Number
Storage
Conditions
RT/RT-PCR Series
Master Premix for first-strand cDNA
synthesis
RT EasyTM I (Master Premix for first-
strand cDNA synthesis)
The reverse transcription temperature of up to 65°C is conducive to the
reverse transcription reaction of complex secondary structure RNA templates
25× 20μl Reactions RT-01011
-20℃
100 × 20μl Reactions RT-01012
Master Premix for first-strand cDNA
synthesis(For qPCR)
RT EasyTM II (Master Premix for first-
strand cDNA synthesis for Real Time PCR)
Optimized reverse transcription primers have been added, only need to add
RNA to perform reverse transcription, and synthesize cDNA directly for
qPCR
200 × 10μl Reactions RT-01022
-20℃
800 × 10μl Reactions RT-01023
Master Premix for first-strand cDNA
synthesis for Real Time PCR with gDNase
(For qPCR)
RT EasyTM II(With gDNase)
Master Premix for first-strand cDNA
synthesis for Real Time PCR with gDNase
This product is a reverse transcription system specially developed for Real
Time PCR to quickly remove genomic DNA contamination. 5× gDNase Mix
can quickly remove the remaining genome in RNA at 42°C for 2 minutes,
effectively avoiding the interference of genome on qPCR results.
100 × 20μl Reactions RT-01032 -20℃
Super Premix for first-strand cDNA
synthesis for lncRNA
Lnc-RT HeroTM I(With gDNase)(Super
Premix for first-strand cDNA synthesis
from lncRNA)
This product is a reverse transcription system specially developed for
LncRNA to quickly remove genomic DNA contamination. 5× gDNase Mix can
quickly remove the remaining genome in RNA at 42°C for 2 minutes,
effectively avoiding the interference of genome on qPCR results.
25 × 20μl Reactions RTL-09098
-20℃
50 × 20μl Reactions RTL-09099
RT-PCR EasyTM I(One Step)
RT-PCR EasyTMI(One Step)
Realize the continuous operation from RT to PCR in the same tube, simple
and fast operation, which can effectively reduce pollution during the
experiment
100 rxns RT-02011
-20℃
500 rxns RT-02012
RT-PCR EasyTM II(Two Step)
RT-PCR EasyTMII(Two Step)
Contains all the reagents for two-step RT-PCR, the unique RT Mix, which
can easily and efficiently synthesize high-quality first-strand cDNA
100 rxns RT-02021
-20℃
500 rxns RT-02022
12. Product Catalogues
Series Product Name Descriptions Specifications
Catalogue
Number
Storage Conditions
RT/RT-PCR Series
RT-qPCR EasyTM I (One Step)-SYBR Green I
RT-qPCR EasyTMI (One Step)-SYBR Green I
The unique system enables the effective combination of RT and Real Time
PCR reactions, which can quickly complete the quantitative detection of
genes.
100 rxns RT-02111
-20℃
500 rxns RT-02112
RT-qPCR EasyTM II (One Step)-Taqman
RT-qPCR EasyTMII (One Step)-Taqman
Rapid and specific real-time RT-PCR quantitative detection of RNA
templates
100 rxns RT-02131
-20℃
500 rxns RT-02132
DNA Marker Series
100bp DNA Ladder
100bp DNA Ladder
The 100bp DNA Ladder is composed of 13 double strands of DNA, of
which the concentration of 200bp, 500bp, and 1000bp is doubled, which
helps to overcome the problem of short fragments that are weak in
brightness and difficult to distinguish bands.
50 Preps DL-20011
4℃
200 Preps DL-20012
1kb DNA Ladder
1kb DNA Ladder
1Kb DNA Ladder is composed of 13 double strands of DNA, of which the
doubled concentration of 1kb and 5kb is helpful to distinguish different
bands
50 Preps DL-30011
4℃
200 Preps DL-30012
Animal Direct PCR
Series
Animal Tissue Direct PCR Kit(65℃lysis)
Animal Tissue Direct PCR Kit(65℃lysis)
Directly use animal tissue lysate as a template for PCR amplification,
without separate extraction of DNA, fast and high sensitivity
200 ×20μl rxns TP-01111
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-01113
Animal Tissue Direct PCR Kit(65℃lysis) -UNG
Animal Tissue Direct PCR Kit(65℃lysis) -UNG
Directly use animal tissue lysate as a template for PCR amplification,
without separate extraction of DNA, fast and high sensitivity. Added UNG
anti-pollution system to eliminate false positives
200 ×20μl rxns TP-01121
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-01123
Mouse Tail SuperDirectTM PCR Kit(room
temperature lysis)
Mouse Tail SuperDirectTM PCR Kit(room
temperature lysis)
Directly use mouse tail lysate as a template for PCR amplification, without
separate extraction of DNA, fast and high sensitivity
200 ×20μl rxns TP-01311
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-01313
13. Product Catalogues
Series Product Name Descriptions Specifications
Catalogue
Number
Storage Conditions
Animal Direct PCR Series
Mouse Tail Direct PCR Kit(65℃lysis)
Mouse Tail Direct PCR Kit(65℃lysis)
Directly use mouse tail lysate as a template for PCR
amplification, without separate extraction of DNA, fast and
high sensitivity
200 ×20μl rxns TP-01331
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-01333
Mouse Tail Direct PCR Kit(65℃lysis) -UNG
Mouse Tail Direct PCR Kit(65℃lysis) -UNG
The mouse tail lysate is directly used as a template for
PCR amplification without separate extraction of DNA,
which is fast and highly sensitive. Added UNG anti-
pollution system to eliminate false positives
200 ×20μl rxns TP-01341
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-01343
Zebra Fish Direct PCR Kit(65℃lysis)
Zebra Fish Direct PCR Kit(65℃lysis)
Directly use zebrafish lysate as a template for PCR
amplification, without separate extraction of DNA, fast and
high sensitivity
200 ×20μl rxns TP-01411
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-01413
Zebra Fish Direct PCR Kit(65℃lysis) -UNG
Zebra Fish Direct PCR Kit(65℃lysis) -UNG
Direct use of zebrafish lysate as a template for PCR
amplification, no separate extraction of DNA, fast and high
sensitivity. Added UNG anti-pollution system to eliminate
false positives
200 ×20μl rxns TP-01421
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-01423
Blood Direct PCR Series
Blood SuperDirectTM PCR Kit (EDTA)
Blood SuperDirectTM PCR Kit (EDTA)
Directly use EDTA anticoagulated whole blood as a
template for PCR amplification, with high sensitivity and
high amplification efficiency
200 ×20μl rxns TP-04111
-20℃
2000 ×20μl rxns TP-04113
Blood SuperDirectTM PCR Kit(EDTA) -UNG
Blood SuperDirectTM PCR Kit(EDTA) -UNG
Directly use EDTA anticoagulated whole blood as a
template for PCR amplification, with high sensitivity and
high amplification efficiency. The UNG anti-pollution
system has been added to prevent false positives.
200 ×20μl rxns TP-04121
-20℃
2000 ×20μl rxns TP-04123
Blood SuperDirectTM PCR Kit(Heparin)
Blood SuperDirectTMPCR Kit(Heparin)
Directly use heparin anticoagulated whole blood as a
template for PCR amplification, with high sensitivity and
high amplification efficiency
200 ×20μl rxns TP-04211
-20℃
2000 ×20μl rxns TP-04213
14. Product Catalogues
Series Product Name Descriptions Specifications
Catalogue
Number
Storage Conditions
Blood Direct PCR Series
Blood SuperDirectTM PCR Kit(Heparin) -UNG
Blood SuperDirectTM PCR Kit(Heparin) -UNG
Directly use heparin anticoagulated whole blood as a template for PCR
amplification, with high sensitivity and high amplification efficiency. The
UNG anti-pollution system has been added to prevent false positives.
200 ×20μl rxns TP-04221
-20℃
2000 ×20μl rxns TP-04223
Plant leaf Direct PCR Series
Plant Leaf Direct PCR Kit
Plant Leaf Direct PCR Kit
Directly use leaf or leaf lysate as a template for PCR amplification, without
separate extraction of DNA, fast and high sensitivity.
200 ×20μl rxns TP-02111
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-02113
Plant Leaf Direct PCR Kit -UNG
Plant Leaf Direct PCR Kit -UNG
Directly use leaf or leaf lysate as a template for PCR amplification, without
separate extraction of DNA, fast and high sensitivity. The UNG anti-
pollution system has been added to prevent false positives.
200 ×20μl rxns TP-02121
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-02123
Plant Leaf Direct PCR Plus Kit(Polysaccharide
polyphenol plant)
Plant Leaf Direct PCR Plus Kit(Polysaccharide
polyphenol plant)
Directly use polysaccharide and polyphenol leaf lysate as a template for
PCR amplification, without separate extraction of DNA, fast and high
sensitivity.
200 ×20μl rxns TP-02131
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-02133
Plant Leaf Direct PCR Plus Kit -UNG
(Polysaccharide polyphenol plant)
Plant Leaf Direct PCR Plus Kit -UNG
(Polysaccharide polyphenol plant)
Directly use polysaccharide and polyphenol leaf lysate as a template for
PCR amplification, without separate extraction of DNA, fast and high
sensitivity. The UNG anti-pollution system has been added to prevent
false positives.
200 ×20μl rxns TP-02141
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-02143
Plant seed Direct PCR
Series
Plant Seed Direct PCR Kit I
Plant Seed Direct PCR Kit I
Direct use of seed lysate as a template for PCR amplification, no separate
extraction of DNA, fast and high sensitivity.
200 ×20μl rxns TP-03111
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-03113
Plant Seed Direct PCR Kit I -UNG
Plant Seed Direct PCR Kit I -UNG
Direct use of seed lysate as a template for PCR amplification, no separate
extraction of DNA, fast and high sensitivity. The UNG anti-pollution
system has been added to prevent false positives.
200 ×20μl rxns TP-03121
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-03123
15. Product Catalogues
Series Product Name Descriptions Specifications
Catalogue
Number
Storage Conditions
Plant seed Direct PCR
Series
Plant Seed Direct PCR Kit II
Plant Seed Direct PCR Kit II
Direct use of seed lysate as a template for PCR amplification, no separate extraction of
DNA, fast and high sensitivity.
200 ×20μl rxns TP-03131
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-03133
Plant Seed Direct PCR Kit II -UNG
Plant Seed Direct PCR Kit II -UNG
Direct use of seed lysate as a template for PCR amplification, no separate extraction of
DNA, fast and high sensitivity. The UNG anti-pollution system has been added to prevent
false positives.
200 ×20μl rxns TP-03141
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-03143
Plant Seed Direct PCR Plus Kit
I(Polysaccharide polyphenol plant)
Plant Seed Direct PCR Plus Kit
I(Polysaccharide polyphenol plant)
Directly use polysaccharide polyphenol seed lysate as a template for PCR amplification,
without separate extraction of DNA, fast and high sensitivity.
200 ×20μl rxns TP-03151
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-03153
Plant Seed Direct PCR Plus Kit I -
UNG(Polysaccharide polyphenol plant)
Plant Seed Direct PCR Plus Kit I -
UNG(Polysaccharide polyphenol plant)
Directly use polysaccharide polyphenol seed lysate as a template for PCR amplification,
without separate extraction of DNA, fast and high sensitivity. The UNG anti-pollution
system has been added to prevent false positives.
200 ×20μl rxns TP-03161
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-03163
Plant Seed Direct PCR Plus Kit II
Plant Seed Direct PCR Plus Kit II
Directly use polysaccharide polyphenol seed lysate as a template for PCR amplification,
without separate extraction of DNA, fast and high sensitivity.
200 ×20μl rxns TP-03171
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-03173
Plant Seed Direct PCR Plus Kit II -
UNG(Polysaccharide polyphenol plant)
Plant Seed Direct PCR Plus Kit II -
UNG(Polysaccharide polyphenol plant)
Directly use polysaccharide polyphenol seed lysate as a template for PCR amplification,
without separate extraction of DNA, fast and high sensitivity. The UNG anti-pollution
system has been added to prevent false positives.
200 ×20μl rxns TP-03181
Part I 4℃,Part II -20℃
2000 ×20μl rxns TP-03183
Direct RT-qPCR Series
Cell Direct RT-qPCR Kit–SYBR Green I
QuickEasyTM Cell Direct RT-qPCR
Kit–SYBR Green I
Cells are lysed directly to release RNA for RT-qPCR; the high tolerance system makes it
unnecessary to purify RNA and directly use cell lysates as RNA templates for RT
reactions. Fast and convenient; high sensitivity, strong specificity, and good stability.
200T DRT-01011
Part I 4℃,Part II -20℃
1000T DRT-01012
18. RNA isolation kit comparison
Toxic reagents such as
phenol and chloroform
Complex operation and
long extraction time
Use DNase to remove
DNA contamination
Do not add any toxic
reagents
Easy to operate
Whole process only 11min
Do not add any enzymes,
use DNA cleaning column
01
02
03
01
02
03
Traditional TRIzol Method Foregene RNA isolation method
20. Future
• A new GMP factory will come to use in Oct-2021, life science reagents will be
produced automatically.
• More IVD products will be R&D and produced based on Direct PCR technology.