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Merck

A2917

Acrylamide/Bis-acrylamide

BioReagent, 19:1 (ratio), Molecular Biology

Sinónimos:

Acrylamide/Bisacrylamide, 19:1 (5% crosslinker), Polyacrylamide solution

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NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
41105319
MDL number:
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grade

Molecular Biology

Quality Level

product line

BioReagent

form

powder

feed ratio

19:1 (ratio)

foreign activity

DNAse (exonuclease), NICKase (endonuclease), RNAse, and protease, none detected

SMILES string

NC(=O)C=C.C=CC(=O)NCNC(=O)C=C

InChI

1S/C7H10N2O2.C3H5NO/c1-3-6(10)8-5-9-7(11)4-2;1-2-3(4)5/h3-4H,1-2,5H2,(H,8,10)(H,9,11);2H,1H2,(H2,4,5)

InChI key

OCQZXMCGTAWGEQ-UHFFFAOYSA-N

General description

Polyacrylamide gels are prepared using acrylamide and bis-acrylamide, where bis-acrylamide is a cross-linking agent. On the other hand, acrylamide is a water soluble monomer which helps in forming a transparent stable insoluble gel.

Application

Ready to reconstitute dry powder blends are accurately pre-blended to produce a 40% (w/v) stock solution for use in protein and nucleic acid electrophoresis. The concentration is based on the total weight of both the acrylamide and bis-acrylamide.
Acrylamide/Bis-acrylamide has been used:
  • in the preparation of urea polyacrylamide gel during a modified cross-linking affinity purification protocol (cCLAP)
  • in microsatellite genotyping and nonfluorescent elastin (ELN) (GT)n polymorphism genotyping
  • in polyacrylamide gel for separation of proteins in SDS-PAGE for western blotting

Features and Benefits

Eliminates the need to weigh toxic acrylamide and bis-acrylamide.

Preparation Note

Reconstitute by slowly adding the indicated amount of distilled water to the container and dissolve contents.
To make up 100 ml of A2917, slowly add 63 ml distilled or deionized water to the container and dissolve contents. Do not divide the solid. This makes 100 ml of a 40% stock solution.
For the 1 Liter size, use 630 mL of water.


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pictograms

Skull and crossbonesHealth hazard

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Carc. 1B - Eye Irrit. 2 - Muta. 1B - Repr. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 1 Oral

target_organs

Peripheral nervous system

Clase de almacenamiento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges



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Preparation of sequencing RNA libraries through chemical Cross-linking coupled to affinity purification (cCLAP) in Saccharomyces cerevisiae
Wang C, et al.
Bio-protocol, 8(19) (2018)
Ana Techniqs in Biotechnology (2011)
Estradiol via estrogen receptor beta influences ROS levels through the transcriptional regulation of SIRT3 in human seminoma TCam-2 cells
Panza S, et al.
Tumour Biology : the Journal of the International Society For Oncodevelopmental Biology and Medicine, 39(5), 1-8 (2017)