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Quantitative PCR primers.
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创建时间：
2017-10-30
相关数据集
Evaluation of the multiplex real-time qRT-PCR assays using clinical specimens.
*Patient types were confirmed by sera detection using the corresponding monoplex assays.
NIAID Data Ecosystem70
Drug resistance patterns using GenoType MTBDR plus assay.
Drug resistance patterns using GenoType MTBDRplus assay.
NIAID Data Ecosystem40
Next Generation Sequencing analysis of VL and VH regions following PCR #2 using standard or rh-PCR primers.
Amplicons for NGS were prepared following cloning of PCR fragments into mammalian expression vectors as outlined in Fig 8A. The average number of full-length reads was determined based on the percenta
NIAID Data Ecosystem30
Comparison of real time PCR results with conventional PCR results on 120 ETEC isolates and 74 E . coli pools.
Comparison of real time PCR results with conventional PCR results on 120 ETEC isolates and 74 E. coli pools.
NIAID Data Ecosystem40
Information of selected genes after evaluation, and characteristics of PCR products and primers used in this analysis.
(a) Accession number of genes found in Fragaria vesca genome (http://www.strawberrygenome.org/andhttp://www.rosaceae.org/) that may be amplified by the designed primer pairs. (b) Theoretical melting t
Figshare2015-12-02 更新30
