• Real-time PCR was performed in duplicate on a serial dilution of 2% total input DNA (20 ng, 4 ng, 0.8 ng, and 0.16 ng) using a real-time PCR detection system and SimpleChIP ® Universal qPCR Master Mix #88989. (cellsignal.com)
  • The NEBNext Microbiome DNA Enrichment Kit is suitable for a wide range of sample types and is compatible with downstream applications including next generation sequencing on all platforms, qPCR and end-point PCR. (neb.com)
  • qPCR was performed using the DTprime Real-Time PCR Cycler (DNA-Technology, Russia) as described in [ 2 ], with test sensitivity of about 1000 viral copies per milliliter of blood/plasma. (biomedcentral.com)
  • Input DNA was quantified by Qubit, whereas the qPCR-based KAPA Library Quantification Kit was used to determine KAPA HyperPrep and TruSeq Nano library yields after adapter ligation. (roche.com)
  • Complete, All-In-One, Ready-To-Use - The MyTREC Kit is "complete" containing all the components necessary to run the Real-Time qPCR Assay. (mytreckit.com)
  • Absolute Quantification - By generating an Absolute Calibration / Standard curve using Real Time qPCR Assay. (mytreckit.com)
  • The MyTREC Real Time qPCR Assay Reagent Kit has been designed and developed for sensitive and accurate quantification of Human TRECs in a blood volume as little as 1 ul. (mytreckit.com)
  • The kit is optimized for standard mode on fast qPCR instruments and standard cycling conditions on standard qPCR machines. (mytreckit.com)
  • The Luna Probe One-Step RT-qPCR Kit (No ROX) is optimized for real-time quantitation of target RNA sequences using hydrolysis probes. (neb.com)
  • In a single tube, RNA is first converted to cDNA by a reverse transcriptase, and then a DNA-dependent DNA polymerase amplifies the cDNA, enabling quantitation via qPCR. (neb.com)
  • Probe-based qPCR/RT-qPCR monitors an increase in fluorescence upon 5´ → 3´ exonuclease cleavage of a quenched, target-specific probe to measure DNA amplification at each cycle of a PCR. (neb.com)
  • In the Luna Probe One-Step RT-qPCR Kit (No ROX), Hot Start Taq DNA Polymerase is combined with a novel WarmStart-activated reverse transcriptase, allowing dual control of enzyme activity via reversible, aptamer-based inhibition. (neb.com)
  • The Luna Probe One-Step RT-qPCR Kit (No ROX) is supplied at 2X concentration and contains Hot-Start Taq DNA Polymerase, dNTPs, and all required buffer components. (neb.com)
  • SYBR Green One-Step qRT-PCR Kit (UDG) uses extracted RNA as a template and qPCR primers to continuously perform reverse transcription and fluorescence quantitative PCR in the same reaction tube. (sbsgenetech.com)
  • The kit includes sufficient reagents for 400 samples and includes multiple bottles of buffers and enzymes measured to enable utilization of one bottle per sample prep batch of up to 96 samples. (qiagen.com)
  • The kits provide all necessary reagents optimized for reliable VZV DNA detection and quantitation for in vitro diagnostic use. (qiagen.com)
  • Our high quality reagents are available for every workflow, including popular DNA assembly methods such as NEBuilder ® HiFi DNA Assembly and NEBridge ® Golden Gate Assembly . (neb.com)
  • Product Overview The MethylFlash Methylated DNA Quantification Bundle (Fluorometric) is an entire set of optimized buffers and reagents to fluorometrically quantify worldwide DNA methylation by significantly measuring ranges of 5-methylcytosine (5-mC) in a microplate-based format. (cellexusinc.com)
  • Several reducing and maleimide reagents were investigated to aid in quantification of total Hcy (tHcy). (cdc.gov)
  • The Investigator STAR Lyse&Prep Kit enables automated purification of genomic DNA from forensic samples using open DNA extraction platforms from third party supplier such as Hamilton, TECAN, or others. (qiagen.com)
  • The Investigator STAR Lyse&Prep Kit reproducibly automate purification of genomic DNA, encountered in forensic and human identity applications. (qiagen.com)
  • Erbay Yigit, David I. Hernandez, Joshua T. Trujillo, Eileen Dimalanta, and C. Donovan Bailey (2014) Genome and Metagenome Sequencing: Using the Human Methyl-Binding Domain to Partition Genomic DNA Derived from Plant Tissues. (neb.com)
  • Unlocking clinically translatable genomic information, including copy number alterations (CNA), from formalin-fixed paraffin-embedded (FFPE) tissue is challenging due to low yields and degraded DNA. (biomedcentral.com)
  • Our technique enables identification of driver and prognostic CNAs in archival patient samples previously deemed unsuitable for genomic analysis due to DNA limitations. (biomedcentral.com)
  • Researchers in Human Genetics and Genomics Advances report that how researchers describe genomic studies may alienate potential participants. (genomeweb.com)
  • Conversion rates for libraries prepared for target capture from different amounts of Covaris-sheared human genomic DNA, using the KAPA HyperPrep or competitor library construction kits. (roche.com)
  • E2F1 CNV was measured in genomic DNA isolated from blood of 552 patients diagnosed with melanoma and 520 healthy subjects using TaqMan Copy Number Assays. (biomedcentral.com)
  • The absence of DNA contamination in RNA samples was confirmed by PCR of GAPDH with primers specific to genomic DNA. (biomedcentral.com)
  • Key sequencing metrics for libraries prepared from 100 ng of FFPE DNA for target capture, using either the KAPA HyperPrep Kit or TruSeq Nano DNA Sample Prep Kit (Illumina). (roche.com)
  • See performance data showing high coverage uniformity using KAPA HyperPrep Kits and minimal amplification bias with KAPA HiFi polymerase. (roche.com)
  • The kit is formulated with TaqMan dual-labeled fluorescent probes and a Gene Expression Master Mix containing antibody-mediated hot-start DNA Polymerase, Enhancers, Stabilizers, dNTPs. (mytreckit.com)
  • This product integrates efficient M-MuLV Reverse Transcriptase, RNase Inhibitor, and the superior antibody-bound hotstart Taq DNA Polymerase, with an optimized buffer system. (sbsgenetech.com)
  • The hotstart Taq DNA Polymerase used in this product is a high-quality, antibody-bound hot start enzyme. (sbsgenetech.com)
  • The Taq enzyme in hotstart Taq DNA Polymerase binds with a monoclonal antibody against the Taq enzyme, inhibiting the Taq enzyme's DNA polymerase activity. (sbsgenetech.com)
  • PCR product melting curves were obtained for real-time PCR reactions performed using SimpleChIP ® Human DNAJB9 Exon 1 Primers. (cellsignal.com)
  • artus VZV PCR Kits are ready-to-use molecular detection kits for real-time PCR. (qiagen.com)
  • artus VZV Kits are based on the amplification and simultaneous detection of a specific region of the VZV genome using real-time PCR. (qiagen.com)
  • PCR product melting curves were obtained for real-time PCR reactions performed using SimpleChIP ® Human β-Actin Promoter Primers. (cellsignal.jp)
  • Methods: Total RNA was isolated from PNN knockdown human corneal epithelial (HCET) cells or Pnn-deficient mouse corneas, and subjected to real-time-PCR (RT-PCR) assays, and the alternatively spliced lncRNAs were counted. (molvis.org)
  • Two micro-liters of Norgens Salmonella enterica Quantified Bacterial DNA Standard and various serial dilutions (blue curves) were used in a 20 µL Salmonella enterica -specific PCR reaction using Norgens 2X PCR Master Mix (#28007), supplemented with SYBR Green I. The real-time PCR reactions were performed on a Bio-Rad CFXReal-Time PCR System. (norgenbiotek.com)
  • The purified DNA is quantified vigorously using multiple methods including spectrophotometry, gel densitometry and real-time PCR. (norgenbiotek.com)
  • The AltoStar® BKV PCR Kit 1.5 is an in vitro diagnostic test, based on real-time PCR technology, for the detection and quantification of BK virus specific DNA in human plasma, whole blood and urine. (diagnostictechnology.com.au)
  • The HIV-1 DNA Test PRO is a real-time PCR assay based on dual-labelled probes that allows for the quantification of total HIV-1 DNA in blood and PBMC samples from HIV-1 positive patients. (diatheva.com)
  • The ready-to-use duplex real-time PCR mix is specific for the amplification of both HIV-1 DNA and the endogenous reference human Telomerase Reverse Transcriptase gene (hTERT), required for relative quantification of HIV-1 copy number. (diatheva.com)
  • The MyTREC Kit, among other components contains a separate ROX stock aliquot and reporter dyes labeled with FAM / VIC making it compatible with all commonly used Real-Time PCR Instruments. (mytreckit.com)
  • The purification procedure is efficient, and purified DNA performs well in downstream analyses, such as quantitative PCR and STR analysis. (qiagen.com)
  • The sequence analyses and quantification of splice variants of candidate lncRNAs, including RP11-295B20.2, RP11-18I14.1, and RP11-322M19.1, demonstrated complex configuration of their splicing changes, with a significant impact of PNN on the process. (molvis.org)
  • Finally, in situ hybridization analyses revealed the presence of RP11-295G20.2 in the nuclei of corneal epithelial cells, but not in the stromal cells of the human cornea, while RP11-322M19.1 was present in epithelial and non-epithelial cells. (molvis.org)
  • PCR reactions should be performed in duplicate and should include a tube with no DNA to control for contamination, and a serial dilution of a 2% total input chromatin DNA (undiluted, 1:5, 1:25, 1:125), which is used to create a standard curve and determine amplification efficiency.2. (cellsignal.com)
  • The DNA samples were amplified on a Pro Flex PCR System (Thermo Fischer, USA), using the Global Filer PCR Amplification Kit (Applied Biosystems, USA). (intechopen.com)
  • In addition, the kits contain a second heterologous amplification system to identify possible PCR inhibition. (qiagen.com)
  • A method often used to overcome the challenge of a limiting amount of DNA is whole genome amplification (WGA) to increase the amount of starting template DNA [ 9 ]. (biomedcentral.com)
  • Norgens Salmonella enterica Quantified Bacterial DNA Standard and various serial dilutions showed consistent amplification down to fewer than 40 copies per reaction. (norgenbiotek.com)
  • Conversion rates for NEBNext libraries cannot be measured directly with the KAPA Library Quantification Kit and were derived from post-amplification yields. (roche.com)
  • Internal Control The HIV-1 RNA Kits uses Internal Control is the full name to whole-process the HIV-1 extraction and amplification process to avoid false negative results. (sansureglobal.com)
  • The kit provides PCR mix that offers robust and consistent performances even in presence of PCR inhibitors and a stringent automatic hot-start, allowing reaction assembly and temporary storage at room temperature prior to PCR amplification. (diatheva.com)
  • This product contains an optimized ratio of high-quality UDG enzyme and dUTP, effectively eliminating the risk of false positives or low CT values caused by product contamination in PCR amplification. (sbsgenetech.com)
  • It is mainly used to eliminate the product contamination issues in PCR amplification. (sbsgenetech.com)
  • The principle of contamination prevention is to add an appropriate amount of dUTP in the PCR reaction, replacing dTTP with dUTP in DNA, forming PCR amplification products containing the dU base. (sbsgenetech.com)
  • In subsequent PCR reactions, the UDG enzyme selectively cuts the single or double-stranded DNA containing dU that might have been contaminated from previous PCR amplification, preventing potential contamination effects on the current PCR amplification. (sbsgenetech.com)
  • A small molecular weight G-protein essential for Nox2 activation, Rac1, is also transcriptionally activated via active DNA methylation-hydroxymethylation. (nature.com)
  • Our aim is to investigate the role of histone methylation (H3K9me3) of Rac1 promoter in dynamic DNA methylation- transcriptional activation. (nature.com)
  • Crosstalk between H3K9me3 and DNA methylation was examined in cells transfected with siRNA of histone trimethyl-transferase, Suv39H1, or Dnmt1 , exposed to high glucose. (nature.com)
  • Thus, H3K9me3 at Rac1 promoter assists in active DNA methylation-hydroxymethylation, activating Rac1 transcription. (nature.com)
  • Compared with LUMA or LINE-1, Alu, and LTR-based assays, MethylFlash™ experience straight quantifies exact worldwide DNA methylation. (cellexusinc.com)
  • To establish the DNA methylation patterns of the promoter CpG islands of 14 "drug-resistance" genes in hepatocellular carcinoma (HCC). (wjgnet.com)
  • We also show that SpCas9-mediated cleavage is unaffected by DNA methylation and that the dosage of SpCas9 and sgRNA can be titrated to minimize off-target modification. (cdc.gov)
  • Magnetic-particle technology combines the speed and efficiency of silica-based DNA purification with the convenient handling of magnetic particles, in a format designed specifically for open DNA extraction platforms. (qiagen.com)
  • In this chapter we will present the usefulness of genetic DNA testing of skeletonized remains for human identification, by using automate DNA extraction from three different human bone types: tooth, femur and petrous pyramid. (intechopen.com)
  • The DNA extraction from bone samples was performed on the automate Maxwell RSC 48 Instrument (Promega, USA), using the Maxwell FSC DNA IQ Casework Kit (Promega, USA). (intechopen.com)
  • Considering that these cases involved DNA extraction from teeth, bones and old human remains, automate system was felt to be the best option to reduce handling errors and increase the possibilities of obtaining good quality DNA. (intechopen.com)
  • Then whole blood and plasma were immediately frozen at −80 °C until DNA extraction. (biomedcentral.com)
  • DNA was extracted from 200 μl aliquots of thawed whole blood or plasma using a standard commercial silica-sorbent kit for DNA extraction from body fluids (Probe-GS® DNA Extraction Kit, DNA-Technology, Russia). (biomedcentral.com)
  • To prevent exogenous contamination, DNA isolation was performed in a separate DNA extraction room (Zone 1). (biomedcentral.com)
  • artus VZV LC, RG, and TM PCR Kits use manual or automated sample preparation and manual assay setup techniques. (qiagen.com)
  • This video walks you through DNA Library Preparation using the NEBNext Ultra II DNA Library Prep Kit. (neb.com)
  • We investigated methods of reducing DNA input and improving performance, including WGA, pre-treatment with a DNA repair procedure, and a low-input WGS library preparation method. (biomedcentral.com)
  • Norgen's Salmonella enterica Quantified Bacterial DNA Standard is prepared from cultured bacteria using Norgen's sample preparation technology. (norgenbiotek.com)
  • KAPA HyperPrep Kits offer a streamlined library preparation protocol that combines several enzymatic steps and eliminates bead cleanups to significantly reduce library preparation time and improve consistency. (roche.com)
  • KAPA HyperPrep Kits offer complete library preparation solution with KAPA Adapters and KAPA Pure Beads. (roche.com)
  • Sequencing preparation involved creating libraries by cloning of DNA reverse transcribed from endogenous small RNAs of 21-25 bp size selected by column and gel electrophoresis. (wikipedia.org)
  • The Luna WarmStart RT Enzyme Mix is supplied at 20X concentration and contains Luna WarmStart Reverse Transcriptase as well as Murine RNase Inhibitor to aid in preventing RNA degradation (see also template preparation in product manual). (neb.com)
  • The kits provide high levels of specificity, sensitivity (see figure " Highly sensitive detection of VZV DNA. Highly sensitive detection of VZV DNA. "> Highly sensitive detection of VZV DNA "), and reproducibility. (qiagen.com)
  • Each method has both common and unique issues related to the required starting DNA amount, specificity, sensitivity, genome coverage, and accuracy as well as cost. (biomedcentral.com)
  • There is no DNA polymerization before denaturation, significantly improving PCR specificity, sensitivity, and quantitative detection accuracy. (sbsgenetech.com)
  • Here, we characterize SpCas9 targeting specificity in human cells to inform the selection of target sites and avoid off-target effects. (cdc.gov)
  • The artus VZV QS-RGQ Kit is part of the QIAsymphony RGQ, the complete automated system from sample to pathogen detection, and is not for use with manual assay setup. (qiagen.com)
  • We describe a robust, cost-effective low-coverage whole genome sequencing (LC WGS) method for CNA detection using 5 ng of FFPE-derived DNA. (biomedcentral.com)
  • Whole genome sequencing (WGS) at 30× coverage can also be used for CNA and LOH detection, but requires at least 100 ng of high quality input DNA and has challenges associated with cost, bioinformatics processing time, and storage of large datasets. (biomedcentral.com)
  • The kit uses next generation sequencing for the detection and identification of mutations in BRAF, EGFR, KRAS, and PIK3CA genes in human cfDNA isolated from blood plasma which play a significant role in the development of NSCLC and are relevant biomarkers for prognosis, choice of therapy as well as monitoring of recurrence and therapy response. (sysmex-europe.com)
  • Sansure's HIV-1 RNA Quantitative Fluorescence Diagnostic Kit is intended for quantitative detection of the HIV-1 Virus RNA in human EDTA plasma specimens. (sansureglobal.com)
  • Nucleic Acid Test Kit for HBV,HCV,HIV(Type1+2), is based on real-time fluorescence PCR technology and used for nucleic acid qualitative detection of HBV, HCV, HIV1+2 in plasma. (sansureglobal.com)
  • The use of COLD-PCR, DHPLC and GeneScanning for the highly sensitive detection of c-KIT somatic mutations in canine mast cell tumours. (cellexusinc.com)
  • Although these biosensors are currently among the less popular tools for human disease detection, they have become useful tools for the screening and detection of pathogenic bacteria, fungi, and viruses because of their versatile advantageous features compared to other sensing devices. (frontiersin.org)
  • The human immunodeficiency virus (HIV) is the causative agent for the worldwide AIDS epidemic, and it has taken nearly 33 million lives worldwide. (sansureglobal.com)
  • However, the presence of coexisting sexually transmitted diseases (eg, human immunodeficiency virus [HIV] infection) appears to increase the risk. (medscape.com)
  • At a point where the fluorescence signal is confidently detected over the background fluorescence, a quantification cycle or C q value can be determined. (neb.com)
  • Applied Biosystems SOLiD sequencing platform has also been used to examine the prognostic value of miRNAs in detecting human breast cancer. (wikipedia.org)
  • The artus VZV RG PCR Kit is also available as EASY artus VZV RG PCR Kits, which include the EZ1 DSP Virus Kit for automated viral nucleic acid purification. (qiagen.com)
  • Total HIV-1 DNA includes an overall quantification of all viral forms of HIV DNA in infected cells, each playing a different role in HIV replication and pathophysiology, monitoring the number of infected cells in a latent or productive state. (diatheva.com)
  • In this lab bacteria are grown to produce DNA, which we use in further experiments such as viral vector production. (lu.se)
  • artus VZV PCR Kits CE are intended for in vitro diagnostic use in Europe. (qiagen.com)
  • This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals. (neb.com)
  • The test results of this diagnostic kit can distinguish reactivity of between HBV, HCV and HIV. (sansureglobal.com)
  • Additionally, researchers at Vanderbilt University are using the assay to discover variants that reliably predict an adverse effect from a medication in 80,000 DNA samples with matched, de-identified medical records. (genomeweb.com)
  • Using the SURVEYOR nuclease assay 13 , we assessed the ability of each Cas9-sgRNA complex to generate indels in human embryonic kidney (HEK) 293FT cells through the induction of DNA doublestranded breaks (DSBs) and subsequent nonhomologous end joining (NHEJ) DNA damage repair (Online Methods). (cdc.gov)
  • SimpleChIP ® Human DNAJB9 Exon 1 Primers were tested on DNA isolated from cross-linked cells using the SimpleChIP ® Plus Enzymatic Chromatin IP Kit (Magnetic Beads) #9005. (cellsignal.com)
  • SimpleChIP ® Human DNAJB9 Exon 1 Primers contain a mix of forward and reverse PCR primers that are specific to exon 1 of the human DnaJ homolog subfamily B member 9 gene. (cellsignal.com)
  • These primers can be used to amplify DNA that has been isolated using chromatin immunoprecipitations (ChIP). (cellsignal.com)
  • SimpleChIP ® Human β-Actin Promoter Primers contain a mix of forward and reverse PCR primers that are specific to a region of the human β-actin promoter. (cellsignal.jp)
  • SimpleChIP ® Human ATF-3 Exon 1 Primers contain a mix of forward and reverse PCR primers that are specific to exon 1 of the human activating transcription factor 3 gene. (cellsignal.jp)
  • This effectively prevents non-specific annealing of primers and template DNA or primer dimer formation at low temperatures. (sbsgenetech.com)
  • This ensures quick, simple operations, minimizing human errors, effectively reducing contamination risk, saving operational time in PCR experiments, and enabling high throughput. (sbsgenetech.com)
  • Alternatively spliced lncRNAs were detected with in situ hybridization with variant-specific RNA probes on human cornea sections. (molvis.org)
  • Next-generation sequencing eliminates the need for sequence specific hybridization probes required in DNA microarray analysis as well as laborious cloning methods required in the Sanger sequencing method. (wikipedia.org)
  • Although the high success rate of CNA by MIP assays in FFPE-derived DNA makes it arguably the best currently used method, its application remains limited since in many research and clinical settings, obtaining 100 ng of input DNA is often unachievable, particularly for small biopsy samples and pre-cancerous lesions. (biomedcentral.com)
  • The kit format is specially designed for high-throughput applications accelerating the laboratory workflow and producing high quantities of high-quality DNA for downstream processing. (qiagen.com)
  • METHODS: A 3.2-mm punch was taken from dried blood spot (DBS) specimens and extracted using a solution containing isotopically labeled internal standards for quantification. (cdc.gov)
  • Another study comparing small RNA profiles of human cervical tumours and normal tissue, utilized the Illumina (company) Genome Analyzer to identify 64 novel human miRNA genes as well as 67 differentially expressed miRNAs. (wikipedia.org)
  • We used the Affymetrix Human Genome U133 A and B GeneChip sets [ 16 ] to establish the gene expression in normal kidney tissues and distinct types of renal cell tumours. (biomedcentral.com)
  • ameba-resistant intracellular bacteria might represent a Taxonomic position of KNic was further defi ned by new etiologic agent of pneumonia because it is likely also sequencing 16Sr RNA ( rrs , DQ635609) and ADP/ATP resistant to human alveolar macrophages ( 2,3 ). (cdc.gov)
  • MicroRNA sequencing (miRNA-seq), a type of RNA-Seq, is the use of next-generation sequencing or massively parallel high-throughput DNA sequencing to sequence microRNAs, also called miRNAs. (wikipedia.org)
  • Sequence library construction can be performed using a variety of different kits depending on the high-throughput sequencing platform being employed. (wikipedia.org)
  • View comparison data for higher conversion of input DNA to adapter-ligated library by KAPA HyperPrep Kit compared to Illumina TruSeq Nano DNA Kits or NEBNext ® Ultra™ II FS Kit. (roche.com)
  • The NEBNext ® Microbiome DNA Enrichment Kit facilitates enrichment of microbial DNA from samples containing methylated host DNA (including human), by selective binding and removal of the CpG-methylated host DNA. (neb.com)
  • The NEBNext® Microbiome DNA Enrichment Kit enables enrichment of non-CpG-methylated DNA from samples contaminated with eukaryotic-cell DNA. (neb.com)
  • The Investigator STAR Lyse&Prep Kit enables highly efficient purification of DNA from forensic casework samples in a high-throughput setup. (qiagen.com)
  • Input volumes can be adjusted to accommodate a larger lysis volume for larger samples and use of the Investigator Lyse&Spin Basket Kit. (qiagen.com)
  • Since the type of samples that can be processed using the Investigator STAR Lyse&Prep Kit can vary greatly, there is also a variety of different pretreatments, optimized for specific sample types. (qiagen.com)
  • Samples are lysed under denaturing conditions, in the presence of proteinase K and Buffer ATL, in total volumes of either 300 µl (intended for routine use) or 500 µl (facilitating the use of the Investigator Lyse&Spin Basket Kit and also processing of larger samples). (qiagen.com)
  • Power Quant System (Promega, USA) was used for DNA quantification of the samples. (intechopen.com)
  • Microbiome DNA analysis can be challenging due to the high percentage of host (eukaryotic) DNA present in many samples. (neb.com)
  • One of the most reliable approaches available to date is molecular inversion probe (MIP) technology, which can obtain high-quality CNA and genotype data from FFPE samples with less than 100 ng of input DNA [ 4 ]. (biomedcentral.com)
  • The human vascular injury panels have been validated for analysis of serum, plasma, and tissue culture samples. (genomeweb.com)
  • Researchers can analyze samples using Aushon's CLIA-certified sample testing service or by conducting the analysis themselves by using the firm's biomarker kits and imaging system. (genomeweb.com)
  • The samples of choice for association studies are usually blood and saliva, however, relatively little is known about how DAE compares in multiple human tissues and it is questionable whether studying DAE in blood would be a proper surrogate for what happens in the disease target tissue. (springer.com)
  • The novel, single-tube chemistry offers further improvements to library construction efficiency, particularly for challenging samples such as FFPE and cell-free DNA. (roche.com)
  • KAPA HyperPrep Kits enable improved coverage depth for FFPE samples. (roche.com)
  • SYBR Green One-Step qRT-PCR Kit (20X, UDG) is a high-quality, carryover prevention premix reagent kit for one-step quantitative reverse transcription PCR (qRT-PCR or real-time RT-PCR) based on SYBR Green dye. (sbsgenetech.com)
  • Determine if your instrument is a High / Low / No ROX instrument and add the ROX stock reference dye to the Gene Expression Master Mix, according to the specifications detailed in the product brochure. (mytreckit.com)
  • CRISPR/Cas9-mediated gene modifying has been leveraged for the modification of human and mouse T cells. (cellexusinc.com)
  • To ensure highest sensitivity, artus VZV Kits have been optimized to detect low numbers of VZV DNA. (qiagen.com)
  • The Plasma-SeqSensei™ (PSS) NSCLC RUO (research use only) Kit detects mutations in circulating tumour DNA (ctDNA) from plasma in patients with non-small cell lung cancer. (sysmex-europe.com)
  • The Investigator STAR Lyse&Prep Kit is intended for molecular biology applications in forensic, human identity, and paternity testing. (qiagen.com)
  • The Investigator STAR Lyse&Prep Kit meets ISO 18385 requirements. (qiagen.com)
  • There is active research into the human microbiome and how it differs between sites like the gut and the skin. (neb.com)
  • Microbiome sample analysis is commonly confounded by the presence of host-cell DNA in the sample. (neb.com)
  • Can microbiome-enrichment techniques be used to partition plant DNA? (neb.com)
  • To generate greater student interest, we have developed an affordable practical lab ($16 dollars per student) where students extract and sequence their own mtDNA and use it for exercises involving phylogenetic reconstruction (placement of own DNA into the world tree), divergence (speciation) time (comparing current student population with chimps, gorillas, and Neanderthal), and population genetics (demographic change calculation based on student's sample). (biomedcentral.com)
  • We find that SpCas9 tolerates mismatches between guide RNA and target DNA at different positions in a sequence-dependent manner, sensitive to the number, position and distribution of mismatches. (cdc.gov)
  • We hypothesized that type 1 diabetes in humans could also be linked to a specific gut microbiota. (biomedcentral.com)
  • It is primarily designed for ultra-sensitive and specific quantification of RNA. (sbsgenetech.com)
  • Mice transduced with both ASXL1 and RUNX1 mutations enhanced inhibitor of DNA binding 1 (ID1) expression in the spleen, liver, and bone marrow cells. (biomedcentral.com)
  • Simply add template DNA to the ready-to-use PCR master mix, and start the reaction on the appropriate real-time cycler using the optimized cycling program described in the kit handbook. (qiagen.com)
  • However, the challenge of obtaining sufficient quantity and quality of DNA from formalin-fixed paraffin-embedded (FFPE) tissue has severely limited adoption of this approach. (biomedcentral.com)
  • TTV has been detected in almost every human tissue type or body fluid reaching near 100% prevalence. (biomedcentral.com)
  • A tissue-culture system using recombinant DNA technology was recently developed and has advanced the scientific knowledge base considerably, including early forays into vaccine development. (medscape.com)
  • For the configuration of the Plasma-SeqSensei™ NSCLC RUO kits, four key cancer genes were selected after comparison of mutation frequencies using the COSMIC (Catalogue of Somatic Mutation in Cancer) and cBioPortal for cancer genomics databases. (sysmex-europe.com)
  • Therefore, there is an urgent need to develop a technique to detect CNA with high accuracy from very limited input of FFPE-derived DNA. (biomedcentral.com)
  • Employing in vitro cell culture of inherited mitochondrial disease and an in vivo animal experimental model of low-grade inflammation (high fat feeding), we show human-derived MSCs to alter mitochondrial function. (frontiersin.org)
  • Students had a 100% rate of success in obtaining DNA sequences and their evaluations report high satisfaction with the learning outcome. (biomedcentral.com)
  • sgRNAs with +67 or +85 nucleotide (nt) tracrRNA tails mediated DNA cleavage at all target sites tested, with up to fivefold higher levels of indels than the corresponding crRNA-tracrRNA duplexes ( Fig. 1b and Supplementary Fig. 1a ). (cdc.gov)
  • Using N-ethylmaleimide (NEM) to selectively derivatize Hcy allowed interferent-free quantification of tHcy by FIA-MS/MS in first-tier NBS. (cdc.gov)
  • WHO specifications under the New Procedure do not necessarily apply to nominal y similar products of other manufacturer(s), nor to those where the active ingredient is produced by other routes of manufacture. (who.int)
  • 1999. Response of normal human keratinocytes to sulfur mustard (HD): Cytokine release using a non-enzymatic detachment procedure. (cdc.gov)
  • In this laboratory-teaching unit, students use their own DNA to place themselves in the humans of the world mtDNA phylogenetic tree (Fig. 1 ) and to deduce and find the geographic origin of their maternal lineage and to estimate population genetic parameters. (biomedcentral.com)
  • Consistent with this, we found that E 2 -treatment of human mast cell lines (HMC-1 and LAD2) resulted in altered cytokine and chemokine expression. (oncotarget.com)
  • Salmonella enterica Quantified Bacterial DNA Standard (Cat. (norgenbiotek.com)
  • To be used as a positive control or PCR quantification standard for Salmonella enterica . (norgenbiotek.com)
  • Upon receipt, store Norgen's Salmonella enterica Quantified Bacterial DNA Standard at -20 o C or lower. (norgenbiotek.com)
  • Salmonella enterica DNA Standard . (norgenbiotek.com)
  • The majority of the 1.3 billion annual cases of Salmonella-caused human gastroenteritis result from ingestion of contaminated food products, such as raw or undercooked meat, seafood, and eggs, as well as raw or unpasteurized milk and dairy products. (norgenbiotek.com)
  • 1991. Genetic activity of the human carcinogen sulphur mustard towards salmonella and the mouse bone marrow. (cdc.gov)
  • UA has been shown to improve mitochondrial health preclinically and in humans. (nature.com)
  • PCR products were run on a 3500 Genetic Analyzer (Thermo Fischer, USA). (intechopen.com)
  • CN profiles using 100 ng or 5 ng input DNA were highly concordant and comparable with molecular inversion probe (MIP) array profiles. (biomedcentral.com)
  • Along with measurement of SARS-CoV-2 RNA in this step, several laboratory controls should also be measured, including matrix recovery controls, human fecal normalization, quantitative measurement controls, and controls to assess molecular method inhibition. (cdc.gov)
  • DNA yield (dark blue bars, ng/µl) and the Ct values (light blue bars) of the internal control of the Investigator Quantiplex Pro RGQ Kit are shown. (qiagen.com)
  • The AltoStar® BKV PCR Kit 1.5 is configured for use with the CFX96™ Deep Well Dx System (Bio-Rad) in combination with the AltoStar® Automation System AM16, the AltoStar® Purification Kit 1.5 and the AltoStar® Internal Control 1.5. (diagnostictechnology.com.au)
  • Using human retinal endothelial cells in 20 mM D-glucose, H3K9me3 at Rac1 promoter was quantified by chromatin-Immunoprecipitation technique. (nature.com)
  • Each peak is formed from the degradation of a single PCR product. (cellsignal.com)