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Data from: Quantitative PCR primer design affects quantification of dsRNA-mediated gene knockdown
负责人:
关键词:
double\u2010stranded RNA;gene knockdown;primer design;RNAi;RT\u2010qPCR
DOI:
doi:10.5061/dryad.28n8d6t
摘要:
in the availability of antibodies for detecting proteins, quantitative PCR (qPCR) remains the preferred method for quantifying target gene knockdown after dsRNA treatment
Data from: Molecular prey identification in Central European piscivores
负责人:
关键词:
Diet Analysis Piscivores Predator Prey Interactions Wildlife Management Diagnostic Multiplex PCR
DOI:
doi:10.5061/dryad.1vf74
摘要:
using conventional morphological analysis of prey remains. Here, we present a two-step multiplex PCR system, comprised of six assays, allowing for rapid
Data from: A method for estimating population sex ratio for sage-grouse using noninvasive genetic samples
负责人:
关键词:
conservation genetics;Population Ecology;Birds;Wildlife Management
DOI:
doi:10.5061/dryad.v0q5p
摘要:
ng polymerase chain reaction (PCR) has become a common method for identifying sex from sources such as hair, feathers, or feces, and is a potential source for estimating sex ratio
Data from: Increasing the accuracy and precision of relative telomere length estimates by RT qPCR
负责人:
关键词:
Telomeres;repeatability;qPCR;Molecular aging;statistical power
DOI:
doi:10.5061/dryad.7356h
摘要:
, the costs of reproduction and disease. qPCR is a high throughput and cost effective tool to measure relative TL (rTL) that can be applied to newly-collected and archived
Data from: Whole transcriptome RNA-Seq analysis of breast cancer recurrence risk using formalin-fixed paraffin-embedded tumor tissue
负责人:
关键词:
RNA-seq;Next Generation Sequencing;transcriptome;Breast Cancer;Homo Sapiens
DOI:
doi:10.5061/dryad.q760h
摘要:
RNA biomarkers discovered by RT-PCR-based gene expression profiling of archival formalin-fixed paraffin-embedded (FFPE) tissue form the basis
Data from: Direct sequencing of haplotypes from diploid individuals through a modified emulsion PCR-based single-molecule sequencing approach
负责人:
关键词:
Eurtytemora affinis
DOI:
doi:10.5061/dryad.rh7f4
摘要:
, we developed a simple PCR-based method for obtaining sequence information from individual DNA strands using standard laboratory equipment. The method employs
Data from: 60 specific eDNA qPCR assays to detect invasive, threatened and exploited freshwater vertebrates and invertebrates in Eastern Canada
负责人:
关键词:
DOI:
doi:10.5061/dryad.12jm63xtw
摘要:
for which monitoring may be challenging. Species detection efforts using a combination of eDNA and qPCR have been highly successful and, as a result, thei
Data from: Multiplexed microsatellite markers for genetic studies of beech
负责人:
关键词:
microsatellites;multiplex PCR;Recent;quality controls;Fagus sylvatica
DOI:
doi:10.5061/dryad.pc8d30j2
摘要:
climate change effects. Multiplex PCR of microsatellites is a fast and cost-effective technique allowing high throughput genotyping. Here we present the procedure use
Data from: Detection of airborne genetically modified maize pollen by real-time PCR
负责人:
Folloni, Silvia
关键词:
Agriculture Biotechnology Genetically Modified Organisms Environmental DNA
DOI:
doi:10.5061/dryad.82th6
摘要:
PCR analysis as an approach to monitor GM maize cultivations in a specific area. Field trial experiments in the European Union and South America demonstrated

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