W1754
PCR Reagent
<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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This Item | W4502 | W3513 | 34877 |
---|---|---|---|
vapor density <1 (vs air) | vapor density <1 (vs air) | vapor density <1 (vs air) | vapor density <1 (vs air) |
vapor pressure 3 mmHg | vapor pressure 3 mmHg | vapor pressure 3 mmHg | vapor pressure 3 mmHg |
form liquid | form liquid | form liquid | form liquid |
technique(s) PCR: suitable | technique(s) PCR: suitable, electrophoresis: suitable | technique(s) cell culture | mammalian: suitable | technique(s) HPLC: suitable |
refractive index n20/D 1.34 (lit.) | refractive index n20/D 1.34 (lit.) | refractive index n20/D 1.34 (lit.) | refractive index n20/D 1.34 (lit.) |
10 - Combustible liquids
nwg
No data available
No data available
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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.
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 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 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.
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