This document summarizes a new UV-visible spectroscopy method for quantifying the number and ratio of unlabeled DNA strands bound to gold nanoparticles (AuNPs) of different sizes. The method allows determining the number of both recognition and diluent DNA sequences on the AuNPs without using fluorescent labels. When applied to AuNPs of 5 nm and 12 nm, the method showed the ratio of DNA sequences bound was different for the different sized AuNPs, suggesting the AuNP radius of curvature influences DNA assembly.
Nucleic acids like DNA and RNA contain genetic information that is passed from generation to generation. There are tools that allow analysis of nucleic acids, like isolating DNA and RNA from cells/samples, electrophoresis to separate molecules by size, PCR to amplify specific DNA sequences, and sequencing to determine the order of nucleotides in DNA or cDNA from RNA. Next generation sequencing now allows high-throughput sequencing of millions of DNA fragments in parallel.
This document discusses the evolution of next-generation sequencing (NGS) technologies over the past decade. It begins by describing how early NGS platforms enabled massively parallel sequencing through the clonal amplification of DNA templates on beads or solid surfaces. It then explains the two main approaches used in NGS - sequencing by ligation (SBL) and sequencing by synthesis (SBS) - and how they identify nucleotide sequences. The document evaluates the benefits and limitations of various NGS platforms and approaches.
This document discusses various methods for labeling nucleic acid probes used in hybridization experiments. It describes five basic methods: nick translation, primer extension, methods using RNA polymerase, end labeling, and direct labeling. Nick translation involves making cuts in double-stranded DNA and using DNA polymerase to replace one strand with a radioactive or biotin-labeled strand. Primer extension involves extending a primer that is complementary to the probe sequence using DNA polymerase and labeled nucleotides. RNA polymerase methods use the enzyme to incorporate labeled nucleotides during transcription. End labeling adds a label to the 3' or 5' end of nucleic acids. The document also discusses factors to consider when choosing a label such as radioactive versus non-radioactive options.
Real time PCR, also known as quantitative PCR or qPCR, allows for both the amplification and simultaneous quantification of targeted DNA sequences. It works by detecting amplified DNA in real time as the reaction progresses, rather than just at the end, as in standard PCR. There are two main methods for detection - using non-specific fluorescent dyes that bind to any double-stranded DNA, or using sequence-specific fluorescent probes. Real time PCR is commonly used for diagnostic applications to detect infectious diseases and cancers, as well as basic research applications to quantify gene expression levels.
PCR can be used for cloning, DNA fingerprinting, gene expression analysis, DNA sequencing, and more. It works by amplifying a specific region of DNA through repeated heating and cooling cycles. This allows very small amounts of DNA to be exponentially multiplied, enabling various applications. PCR was invented in 1983 by Kary Mullis and revolutionized molecular biology.
The document describes a simplified "pipette, aggregate and blot" (PAB) method for label-free DNA quantification using magnetic beads. The method involves mixing DNA samples with magnetic beads in a pipette tip, exposing them to a magnetic field to induce bead aggregation, blotting the mixture onto filter paper, and analyzing digital images of the aggregates to quantify DNA concentration. Compared to conventional techniques, the PAB method requires only simple, inexpensive materials and has potential for integration into point-of-care diagnostic devices to quantify DNA samples prior to downstream analysis.
Polymerase Chain Reaction: Principles, Applications, and Advancements | The L...The Lifesciences Magazine
Polymerase Chain Reaction, often abbreviated as PCR, is a laboratory technique used to amplify specific segments of DNA through a series of temperature-controlled cycles.
This document summarizes a new UV-visible spectroscopy method for quantifying the number and ratio of unlabeled DNA strands bound to gold nanoparticles (AuNPs) of different sizes. The method allows determining the number of both recognition and diluent DNA sequences on the AuNPs without using fluorescent labels. When applied to AuNPs of 5 nm and 12 nm, the method showed the ratio of DNA sequences bound was different for the different sized AuNPs, suggesting the AuNP radius of curvature influences DNA assembly.
Nucleic acids like DNA and RNA contain genetic information that is passed from generation to generation. There are tools that allow analysis of nucleic acids, like isolating DNA and RNA from cells/samples, electrophoresis to separate molecules by size, PCR to amplify specific DNA sequences, and sequencing to determine the order of nucleotides in DNA or cDNA from RNA. Next generation sequencing now allows high-throughput sequencing of millions of DNA fragments in parallel.
This document discusses the evolution of next-generation sequencing (NGS) technologies over the past decade. It begins by describing how early NGS platforms enabled massively parallel sequencing through the clonal amplification of DNA templates on beads or solid surfaces. It then explains the two main approaches used in NGS - sequencing by ligation (SBL) and sequencing by synthesis (SBS) - and how they identify nucleotide sequences. The document evaluates the benefits and limitations of various NGS platforms and approaches.
This document discusses various methods for labeling nucleic acid probes used in hybridization experiments. It describes five basic methods: nick translation, primer extension, methods using RNA polymerase, end labeling, and direct labeling. Nick translation involves making cuts in double-stranded DNA and using DNA polymerase to replace one strand with a radioactive or biotin-labeled strand. Primer extension involves extending a primer that is complementary to the probe sequence using DNA polymerase and labeled nucleotides. RNA polymerase methods use the enzyme to incorporate labeled nucleotides during transcription. End labeling adds a label to the 3' or 5' end of nucleic acids. The document also discusses factors to consider when choosing a label such as radioactive versus non-radioactive options.
Real time PCR, also known as quantitative PCR or qPCR, allows for both the amplification and simultaneous quantification of targeted DNA sequences. It works by detecting amplified DNA in real time as the reaction progresses, rather than just at the end, as in standard PCR. There are two main methods for detection - using non-specific fluorescent dyes that bind to any double-stranded DNA, or using sequence-specific fluorescent probes. Real time PCR is commonly used for diagnostic applications to detect infectious diseases and cancers, as well as basic research applications to quantify gene expression levels.
PCR can be used for cloning, DNA fingerprinting, gene expression analysis, DNA sequencing, and more. It works by amplifying a specific region of DNA through repeated heating and cooling cycles. This allows very small amounts of DNA to be exponentially multiplied, enabling various applications. PCR was invented in 1983 by Kary Mullis and revolutionized molecular biology.
The document describes a simplified "pipette, aggregate and blot" (PAB) method for label-free DNA quantification using magnetic beads. The method involves mixing DNA samples with magnetic beads in a pipette tip, exposing them to a magnetic field to induce bead aggregation, blotting the mixture onto filter paper, and analyzing digital images of the aggregates to quantify DNA concentration. Compared to conventional techniques, the PAB method requires only simple, inexpensive materials and has potential for integration into point-of-care diagnostic devices to quantify DNA samples prior to downstream analysis.
Polymerase Chain Reaction: Principles, Applications, and Advancements | The L...The Lifesciences Magazine
Polymerase Chain Reaction, often abbreviated as PCR, is a laboratory technique used to amplify specific segments of DNA through a series of temperature-controlled cycles.
Biotechnological approaches in aquatic animal health managementThavasimuthu citarasu
This document provides information about Dr. T. Citarasu and his work at Manonmaniama Sundaranar University focusing on biotechnological approaches for aquatic animal health management and improved aquaculture production. It discusses diagnostic tools like PCR, challenges with disease control, and how genomics, proteomics, immunodiagnosis, and in silico drug design can help address issues in the aquaculture industry.
This document provides an overview of polymerase chain reaction (PCR) including its history, principles, components, cycle, limitations, advantages, disadvantages, types, and applications. PCR is described as an in vitro method for enzymatically synthesizing specific DNA sequences using two oligonucleotide primers that flank the target region. It allows for exponential amplification of minute amounts of DNA. Real-time PCR is highlighted as an advancement that provides ease of quantification, greater sensitivity, reproducibility, and precision compared to traditional PCR. The document also reviews various applications of PCR in fields such as medicine, forensics, and research.
Chromogenic in situ hybridization (CISH) is a technique that combines in situ hybridization with immunohistochemistry to detect specific DNA sequences within tissue samples using brightfield microscopy. CISH uses nucleic acid probes labeled with enzymes that produce colored precipitates when exposed to chromogenic substrates, allowing visualization of gene amplification or rearrangements. CISH has advantages over fluorescence in situ hybridization (FISH) in being cheaper, more stable, and easier to use, though it is less sensitive than FISH. CISH is commonly used to assess HER2 gene amplification in breast cancer and detect genetic fusions in cancers.
A next-generation ultrasensitive electrochemiluminescence assay for human Tau was developed by Meso Scale Discovery with a limit of detection of 6 fg/mL, over 1000x more sensitive than other available assays. This enabled measurement of Tau levels in serum and plasma samples. Tau was detectable in all normal, Alzheimer's, and traumatic brain injury samples tested, with median concentrations of 1.7 pg/mL, 2.6 pg/mL, 3.6 pg/mL, and 13 pg/mL respectively. The new assay provides a sensitive and reproducible method for quantifying Tau concentrations in blood and CSF.
DNA nanoball sequencing is a high-throughput sequencing method that determines the entire genomic sequence of an organism. It uses rolling circle replication to amplify small DNA fragments into DNA nanoballs. Fluorescent probes then bind to complementary DNA sequences on the nanoballs, and the probes' colors are recorded to identify the sequence. The method allows for high DNA concentration and adding new probes without disrupting the reaction. It has been used to identify mutations in cancer samples and estimate inter-generational mutation rates.
This powerpoint explains about the nucleic acid hybridization, its principle, application and the assay methods. Also it gives clear picture about DNA probes, its sysnthesis, mechanism of probes and the detector system in DNA hybridization.
REAL TIME PCR, principle of real time pcr, method for detection real time pcr, taq man probe, molecular beacons. application of real time pcr. difference between real time pcr and conventional pcr.
Fluorometer is a benchtop dual-channel fluorometry meticulously crafted to ensure the accurate detection of highly sensitive fluorescence signals while allowing
the quantification of DNA, RNA, and proteins. With precision excitation filters at 460 ± 20 nm and 525 ± 20 nm, it boasts an impressive sensitivity, detecting DNA
at levels as low as 0.5 ng/ul. Provides dual-channel fluorescence capabilities, featuring both blue and green channels for measuring the concentration of the sample.
Polymerase chain reaction (PCR) is a technique used to amplify specific DNA sequences. It involves cycling between high and low temperatures to separate DNA strands and allow for replication. This allows for targeted amplification of millions of copies of a particular DNA sequence. Real-time quantitative PCR (qPCR) allows for detection and quantification of DNA during amplification through the use of fluorescent probes. Reverse transcription PCR (RT-PCR) first converts RNA to DNA before amplification. PCR techniques like qRT-PCR are currently used for accurate diagnosis of COVID-19 by detecting the SARS-CoV-2 virus from samples.
The document provides an overview of polymerase chain reaction (PCR) techniques. It begins with an introduction to molecular biology techniques and the importance of hands-on experience. It then describes several key molecular techniques including PCR, gel electrophoresis, northern blotting, and southern blotting. The bulk of the document focuses on describing PCR in detail, including its history, components, steps, types, applications, advantages, and limitations. It also briefly discusses gel electrophoresis and provides an overview of the northern blotting process.
Polymerase chain reaction (PCR) is a technique used to amplify specific DNA sequences. It allows targeted DNA sequences to be selectively amplified millions of fold in a few hours. PCR consists of repeated cycles of heating and cooling of the DNA sample to denature and replicate the targeted sequence using DNA polymerase and primers. The amplified DNA can then be analyzed using gel electrophoresis. PCR has many applications including DNA cloning, gene expression analysis, DNA fingerprinting, paternity testing, and detecting infectious diseases and genetic mutations. The researcher aims to identify novel single nucleotide polymorphisms (SNPs) in the UGT1A7 gene in Circassian and Chechen subpopulations compared to Jordanians which may impact the metabolism of ir
In this presentation you will get a deep insight on the most important step of DNA fingerprinting that is the Quantitation of DNA.
You will understand what is DNA quantitation and also about the different techniques of DNA quantitation.
The above presentation consist of the definition of microarray, brief history, general principle of the same, the type of scanner that are used to read or to scan the microarray , type of DNA microarray and finally its various apliccation including the role of DNA microaarray in drug discovery.
In this ppt, the various types of PCR such as real time PCR, Reverse transcription PCR, multiplex PCR, ligation chain PCR, nested PCR which is applied in diagnosis of diseases, identification of genetic disorders, determination of polymorphism and also in DNA fingerprinting analysis are described.
It contains information about- DNA Sequencing; History and Era sequencing; Next Generation Sequencing- Introduction, Workflow, Illumina/Solexa sequencing, Roche/454 sequencing, Ion Torrent sequencing, ABI-SOLiD sequencing; Comparison between NGS & Sangers and NGS Platforms; Advantages and Applications of NGS; Future Applications of NGS.
Next generation sequencing has revolutionized DNA sequencing by allowing millions of DNA fragments to be sequenced in parallel. This has increased sequencing speed and reduced costs. NGS is now used for applications like genome sequencing, transcriptome analysis, metagenomics, and studying genetic variation. It has provided insights into molecular biology and genomics that were not possible with previous sequencing methods.
SLIDE CONTAIN BREIF NOTE ON PCR. IT CONTAINS 21 SLIDES INCLUDING, WHAT IS PCR? COMPONENTS, WORKING MECHANISM, APPLICATIONS, CONCLUSION, AND SOME REFRENCES, HISTORY ALSO
Biotechnological approaches in aquatic animal health managementThavasimuthu citarasu
This document provides information about Dr. T. Citarasu and his work at Manonmaniama Sundaranar University focusing on biotechnological approaches for aquatic animal health management and improved aquaculture production. It discusses diagnostic tools like PCR, challenges with disease control, and how genomics, proteomics, immunodiagnosis, and in silico drug design can help address issues in the aquaculture industry.
This document provides an overview of polymerase chain reaction (PCR) including its history, principles, components, cycle, limitations, advantages, disadvantages, types, and applications. PCR is described as an in vitro method for enzymatically synthesizing specific DNA sequences using two oligonucleotide primers that flank the target region. It allows for exponential amplification of minute amounts of DNA. Real-time PCR is highlighted as an advancement that provides ease of quantification, greater sensitivity, reproducibility, and precision compared to traditional PCR. The document also reviews various applications of PCR in fields such as medicine, forensics, and research.
Chromogenic in situ hybridization (CISH) is a technique that combines in situ hybridization with immunohistochemistry to detect specific DNA sequences within tissue samples using brightfield microscopy. CISH uses nucleic acid probes labeled with enzymes that produce colored precipitates when exposed to chromogenic substrates, allowing visualization of gene amplification or rearrangements. CISH has advantages over fluorescence in situ hybridization (FISH) in being cheaper, more stable, and easier to use, though it is less sensitive than FISH. CISH is commonly used to assess HER2 gene amplification in breast cancer and detect genetic fusions in cancers.
A next-generation ultrasensitive electrochemiluminescence assay for human Tau was developed by Meso Scale Discovery with a limit of detection of 6 fg/mL, over 1000x more sensitive than other available assays. This enabled measurement of Tau levels in serum and plasma samples. Tau was detectable in all normal, Alzheimer's, and traumatic brain injury samples tested, with median concentrations of 1.7 pg/mL, 2.6 pg/mL, 3.6 pg/mL, and 13 pg/mL respectively. The new assay provides a sensitive and reproducible method for quantifying Tau concentrations in blood and CSF.
DNA nanoball sequencing is a high-throughput sequencing method that determines the entire genomic sequence of an organism. It uses rolling circle replication to amplify small DNA fragments into DNA nanoballs. Fluorescent probes then bind to complementary DNA sequences on the nanoballs, and the probes' colors are recorded to identify the sequence. The method allows for high DNA concentration and adding new probes without disrupting the reaction. It has been used to identify mutations in cancer samples and estimate inter-generational mutation rates.
This powerpoint explains about the nucleic acid hybridization, its principle, application and the assay methods. Also it gives clear picture about DNA probes, its sysnthesis, mechanism of probes and the detector system in DNA hybridization.
REAL TIME PCR, principle of real time pcr, method for detection real time pcr, taq man probe, molecular beacons. application of real time pcr. difference between real time pcr and conventional pcr.
Fluorometer is a benchtop dual-channel fluorometry meticulously crafted to ensure the accurate detection of highly sensitive fluorescence signals while allowing
the quantification of DNA, RNA, and proteins. With precision excitation filters at 460 ± 20 nm and 525 ± 20 nm, it boasts an impressive sensitivity, detecting DNA
at levels as low as 0.5 ng/ul. Provides dual-channel fluorescence capabilities, featuring both blue and green channels for measuring the concentration of the sample.
Polymerase chain reaction (PCR) is a technique used to amplify specific DNA sequences. It involves cycling between high and low temperatures to separate DNA strands and allow for replication. This allows for targeted amplification of millions of copies of a particular DNA sequence. Real-time quantitative PCR (qPCR) allows for detection and quantification of DNA during amplification through the use of fluorescent probes. Reverse transcription PCR (RT-PCR) first converts RNA to DNA before amplification. PCR techniques like qRT-PCR are currently used for accurate diagnosis of COVID-19 by detecting the SARS-CoV-2 virus from samples.
The document provides an overview of polymerase chain reaction (PCR) techniques. It begins with an introduction to molecular biology techniques and the importance of hands-on experience. It then describes several key molecular techniques including PCR, gel electrophoresis, northern blotting, and southern blotting. The bulk of the document focuses on describing PCR in detail, including its history, components, steps, types, applications, advantages, and limitations. It also briefly discusses gel electrophoresis and provides an overview of the northern blotting process.
Polymerase chain reaction (PCR) is a technique used to amplify specific DNA sequences. It allows targeted DNA sequences to be selectively amplified millions of fold in a few hours. PCR consists of repeated cycles of heating and cooling of the DNA sample to denature and replicate the targeted sequence using DNA polymerase and primers. The amplified DNA can then be analyzed using gel electrophoresis. PCR has many applications including DNA cloning, gene expression analysis, DNA fingerprinting, paternity testing, and detecting infectious diseases and genetic mutations. The researcher aims to identify novel single nucleotide polymorphisms (SNPs) in the UGT1A7 gene in Circassian and Chechen subpopulations compared to Jordanians which may impact the metabolism of ir
In this presentation you will get a deep insight on the most important step of DNA fingerprinting that is the Quantitation of DNA.
You will understand what is DNA quantitation and also about the different techniques of DNA quantitation.
The above presentation consist of the definition of microarray, brief history, general principle of the same, the type of scanner that are used to read or to scan the microarray , type of DNA microarray and finally its various apliccation including the role of DNA microaarray in drug discovery.
In this ppt, the various types of PCR such as real time PCR, Reverse transcription PCR, multiplex PCR, ligation chain PCR, nested PCR which is applied in diagnosis of diseases, identification of genetic disorders, determination of polymorphism and also in DNA fingerprinting analysis are described.
It contains information about- DNA Sequencing; History and Era sequencing; Next Generation Sequencing- Introduction, Workflow, Illumina/Solexa sequencing, Roche/454 sequencing, Ion Torrent sequencing, ABI-SOLiD sequencing; Comparison between NGS & Sangers and NGS Platforms; Advantages and Applications of NGS; Future Applications of NGS.
Next generation sequencing has revolutionized DNA sequencing by allowing millions of DNA fragments to be sequenced in parallel. This has increased sequencing speed and reduced costs. NGS is now used for applications like genome sequencing, transcriptome analysis, metagenomics, and studying genetic variation. It has provided insights into molecular biology and genomics that were not possible with previous sequencing methods.
SLIDE CONTAIN BREIF NOTE ON PCR. IT CONTAINS 21 SLIDES INCLUDING, WHAT IS PCR? COMPONENTS, WORKING MECHANISM, APPLICATIONS, CONCLUSION, AND SOME REFRENCES, HISTORY ALSO
Similar to DNA quantification by flourimeter d.pptx (20)
This document defines and provides examples of the different types of adverbs in English. It explains that adverbs modify verbs by providing information about how, where, how many times, or with what intensity an action occurs. The types of adverbs discussed are: manner, place, time, frequency, degree, affirmation/negation, and reason. Examples are given for each type to illustrate how adverbs provide additional details about verbs.
This document provides a 3 paragraph summary of the contents and purpose of William Shakespeare's collection of sonnets. The first paragraph introduces that it is an electronic publication from The Electronic Classics Series. The second paragraph notes that Jim Manis is the editor and it is being published to make the works freely accessible. The third paragraph provides background on Jim Manis and notes that the text of the sonnets themselves are not copyrighted within the United States.
it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
A workshop hosted by the South African Journal of Science aimed at postgraduate students and early career researchers with little or no experience in writing and publishing journal articles.
Thinking of getting a dog? Be aware that breeds like Pit Bulls, Rottweilers, and German Shepherds can be loyal and dangerous. Proper training and socialization are crucial to preventing aggressive behaviors. Ensure safety by understanding their needs and always supervising interactions. Stay safe, and enjoy your furry friends!
How to Add Chatter in the odoo 17 ERP ModuleCeline George
In Odoo, the chatter is like a chat tool that helps you work together on records. You can leave notes and track things, making it easier to talk with your team and partners. Inside chatter, all communication history, activity, and changes will be displayed.
How to Fix the Import Error in the Odoo 17Celine George
An import error occurs when a program fails to import a module or library, disrupting its execution. In languages like Python, this issue arises when the specified module cannot be found or accessed, hindering the program's functionality. Resolving import errors is crucial for maintaining smooth software operation and uninterrupted development processes.
Introduction to AI for Nonprofits with Tapp NetworkTechSoup
Dive into the world of AI! Experts Jon Hill and Tareq Monaur will guide you through AI's role in enhancing nonprofit websites and basic marketing strategies, making it easy to understand and apply.
বাংলাদেশের অর্থনৈতিক সমীক্ষা ২০২৪ [Bangladesh Economic Review 2024 Bangla.pdf] কম্পিউটার , ট্যাব ও স্মার্ট ফোন ভার্সন সহ সম্পূর্ণ বাংলা ই-বুক বা pdf বই " সুচিপত্র ...বুকমার্ক মেনু 🔖 ও হাইপার লিংক মেনু 📝👆 যুক্ত ..
আমাদের সবার জন্য খুব খুব গুরুত্বপূর্ণ একটি বই ..বিসিএস, ব্যাংক, ইউনিভার্সিটি ভর্তি ও যে কোন প্রতিযোগিতা মূলক পরীক্ষার জন্য এর খুব ইম্পরট্যান্ট একটি বিষয় ...তাছাড়া বাংলাদেশের সাম্প্রতিক যে কোন ডাটা বা তথ্য এই বইতে পাবেন ...
তাই একজন নাগরিক হিসাবে এই তথ্য গুলো আপনার জানা প্রয়োজন ...।
বিসিএস ও ব্যাংক এর লিখিত পরীক্ষা ...+এছাড়া মাধ্যমিক ও উচ্চমাধ্যমিকের স্টুডেন্টদের জন্য অনেক কাজে আসবে ...
2. DNA & RNA Quantification via Fluorometric Analysis:
Nucleic acid quantification,encomassing Double stranded DNA(dsDNA), Single
stranded DNA(ssDNA) and RNA quantification,
Is a staple process in life science applications requiring and knowledge of
sample concentration Prior to downstream and experiment s.
Both type of nucleic acid are typically quentized
Using one of two optical technologies:
3. Ultraviolet Visible spectroscopy
Fluorescence measurements
Accurately quantifying nucleic acid concentrations is critical for downstream
applications such as next-generation sequencing, transfection, PCR and cloning. Such
applications frequently require a target range of nucleic acid concentration and purity
for optimum performance and inaccurate determination of concentrations can cause
higher variability or assay failure.
4. The Principals of FluoromeAnalysislysis:
Fluorometric analysis provides sensitivity at around 1,000 times higher than absorbance-based methods.
It is also a feature of fluorescence assays that they are highly specific to the analyte of interest compared to
those absorbance.
Quantification of DNA, RNA or Protein through fluorometric methods require the binding of analyte-
specific fluorophores to the sample of interest. The sample/fluorophore complex is illuminated with a
specified excitation wavelength from a light source. The fluorophore emits light over a characteristic spectrum
and the amount of emitted light is proportional to the amount of analyte in the sample. The light is captured
and recorded as relative fluorescent units (RFUs). The concentration of unknown samples can be understood
through the correlation to a standard curve of known concentration samples.
5. Fluorometric Analysis Equipment from DeNovi:
The DS-11 Series and QFX fluorometer from DeNovix are at the forefront of
fluorometric analysis equipment, being more sensitive and reproducible than any other
instrument in its class. The QFX is a powerful solution for fluorometric applications where
improved sensitivity or specificity is required while the DS-11 Series combines microvolume and
cuvette absorbance with fluorescence for total sample quantification method flexibility.
DeNovix Fluorometers have four fluorescent channels for quantification enabling compatibility
with all major quantification assays as well as future-proofing labs for future assay
developments.
6. Using the DeNovix Fluorescence quantification assays, researchers can
quantify dsDNA between 0.5 pg/µL and 4000 ng/µL and a single RNA assay quantifies
in the range of 250 pg/µL to 1500 ng/µL. Each assay is well-suited solution for
quantification of degraded or low concentration samples, even with common
contaminants present.
If you would like to find out more about the fluorometric analysis solutions that
DeNovix can offer, please contact us today.