TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

$ 502.00
  • By A Mystery Man Writer
  • 5(468)
TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

Product Description

The TaqMan Universal RNA Spike In/Reverse Transcription (Xeno) Control is a synthetic RNA control that serves as an exogenous process control for nucl

For use with TaqMan Gene Expression Cells-to-CT Kit Confirm sufficient cell input Monitor the presence of RT or real-time PCR inhibitors Use as an

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

TaqMan™ Cells-to-CT™ Control Kit

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

Single-cell analysis of human ovarian cortex identifies distinct cell populations but no oogonial stem cells

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

[RQ2110] ExcelRT™ One-Step RT-qPCR Kit (TaqMan, ROX), 200 RXN

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

Reverse transcription–polymerase chain reaction (RT–PCR) analysis of

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

Quantitative analysis of miRNAs using SplintR ligase-mediated ligation of complementary-pairing probes enhanced by RNase H (SPLICER)-qPCR - ScienceDirect

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

Comparing the performance of RNA-seq kits for inputs of varying sample type and quality

The TrueMark Comprehensive Microbiota Control contains a linearized multi-target plasmid pool with microbial target sequences commonly used on Custom

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

Applied Biosystems™ TrueMark™ Comprehensive Microbiota Control

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

Frontiers Validation of a multiplex reverse transcription and pre-amplification method using TaqMan® MicroRNA assays

TaqMan™ Universal RNA Spike In/Reverse Transcription (Xeno) Control

Quantitative analysis of miRNAs using SplintR ligase-mediated ligation of complementary-pairing probes enhanced by RNase H (SPLICER)-qPCR - ScienceDirect