Merck
All Photos(1)

W1754

Sigma-Aldrich

Water

PCR Reagent

Linear Formula:
H2O
CAS Number:
Molecular Weight:
18.02
Beilstein:
2050024
Número de EC:
Número MDL:
ID de la sustancia en PubChem:
NACRES:
NA.25

grado

PCR Reagent

Nivel de calidad

200

densidad de vapor

<1 (vs air)

presión de vapor

3 mmHg

esterilidad

sterile-filtered

formulario

liquid

envase

vial of 1.5 mL

technique(s)

PCR: suitable

índice de refracción

n20/D 1.34 (lit.)

pH

5-7

bp

100 °C (lit.)

mp

0 °C (lit.)

densidad

1.000 g/mL at 3.98 °C (lit.)

actividad extraña

DNase, none detected
RNase, none detected

SMILES string

O

InChI

1S/H2O/h1H2

InChI key

XLYOFNOQVPJJNP-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Descripción general

PCR grade water is sterile-filtered. It is free from exonucleases (DNAse, RNAse) and endonuclease (NICKase) and is also free from nucleic acid contamination.

Aplicación

Water has been used to make up the final volume of the sample in polymerase chain reaction (PCR).

Idoneidad

Suitable for polymerase chain reaction (PCR)

Otras notas

Easily compare specifications for Water products with the Water specification table.

Código de clase de almacenamiento

10 - Combustible liquids

WGK

nwg

Punto de inflamabilidad F

No data available

Punto de inflamabilidad C

No data available

Equipo de protección personal

Eyeshields, Gloves

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

Articles

Examination of Efficacy, Specificity, and Efficiency of an shRNA Lentiviral Library

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.

Examination of Efficacy, Specificity and Efficiency of an shRNA Lentiviral Library

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.

Protocols

SYBR® Green JumpStart™ Taq ReadyMix™

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.

Hot Start dNTP protocol to reduce non-specific amplification

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.

Long and Accurate PCR Amplification of DNA (D8045)

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 Protocol (One-step Probe Detection)

Reverse transcription (RT) is the process of converting RNA to cDNA using a reverse transcriptase enzyme and dNTPs.

See All

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service