M8787
300
PCR Reagent
liquid
vial of 1.5 mL
25 mM±1 mM
PCR: suitable
colorless
agriculture
diagnostic assay manufacturing
DNase, RNase, none detected
2-8°C
Cl[Mg]Cl
1S/2ClH.Mg/h2*1H;/q;;+2/p-2
TWRXJAOTZQYOKJ-UHFFFAOYSA-L
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12 - Non Combustible Liquids
nwg
Not applicable
Not applicable
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Method outlines use of a hot start Taq for multiplex qPCR and provides guidance on how to optimize dNTPs, primer, probes and MgCL2 concentrations. By optimizing these parameters, the user can improve assay sensitivity and linear range of detection.
The assessment of DNA quality is a crucial first step in acquiring meaningful data from formalin-fixed paraffin-embedded (FFPE) tissues, and other sources of damaged DNA. Using intact genomic DNA is key for successful analysis of chromosomal aberrations (e.g. SNP analysis, LOH, aCGH, etc.).
Introduction of small interfering RNAs (siRNAs) into cultured cells provides a fast and efficient means of knocking down gene expression and has allowed siRNAs to quickly become a ubiquitous tool in molecular biology.
Our SYBR Green qPCR Protocol is a method designed to detect accurate quantification of gene expression and RT-PCR reactions
Creating Transgenic Mice using CRISPR-Cas9 Genome Editing
Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.
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