W1754
PCR Reagent
200
<1 (vs air)
3 mmHg
sterile-filtered
liquid
vial of 1.5 mL
PCR: suitable
n20/D 1.34 (lit.)
5-7
100 °C (lit.)
0 °C (lit.)
1.000 g/mL at 3.98 °C (lit.)
DNase, none detected
RNase, none detected
O
1S/H2O/h1H2
XLYOFNOQVPJJNP-UHFFFAOYSA-N
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10 - Combustible liquids
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Eyeshields, Gloves
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The 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.
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.
Protocol describes amplification of DNA through quantitative PCR with SYBR Green. Consistent batch-to-batch performance can be achieved with large numbers of PCR reactions.
Protocol using hot start dNTPs. Method includes modified nucleoside triphosphates that block DNA polymerase nucleotide incorporation during hot start PCR to increase specificity. Compatible with a variety of PCR reagents.
Protocol for high fidelity amplification of long PCR fragments up to 22kb from complex DNA mixtures and up to 40kb from simple DNA mixtures. AccuTaq LA.
Reverse transcription (RT) is the process of converting RNA to cDNA using a reverse transcriptase enzyme and dNTPs.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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