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Merck

126615

Bovine Serum Albumin

10% Aqueous Solution

Synonyme(s) :

Albumin, Bovine Serum, 10% Aqueous Solution

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About This Item

Numéro CAS:
9048-46-8
MDL number:
MFCD00198176
UNSPSC Code:
12352202
NACRES:
NA.25

Nom du produit

Albumin, Bovine Serum, 10% Aqueous Solution,

biological source

bovine

description

Merck USA index - 14, 8468

form

liquid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze

concentration

1 g/10 mL (Aqueous Solution)

technique(s)

ELISA: suitable
PCR: suitable
immunoblotting: suitable

impurities

≤0.02% Fatty acids
≤10 ppm Heavy metal
≤2.0% Ash

foreign activity

Nuclease, none detected
Protease, none detected

shipped in

ambient

storage temp.

2-8°C

Quality Level

300

Catégories apparentées

Disclaimer

Toxicity: Standard Handling (A)

General description

Purified chromatographically to reduce DNases and RNases to exceptionally low levels.
Useful for applications in which acetylated BSA is not desirable, such as in antibody dilution, DNA footprinting and gel shift assay, ELISA, enzyme assay, enzyme stabilization, immunoblotting, immunofluorescence, PCR, restriction enzyme reactions, RIA, probe-based diagnostics, radioactive quenching, and receptor binding studies. Purified chromatographically to reduce DNases and RNases to exceptionally low levels.

Physical form

10% aqueous solution, 0.22 µm-filtered, pH 6.8-7.2.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Classe de stockage

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificats d'analyse (COA)

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Alan J Simmons et al.
STAR protocols, 3(3), 101570-101570 (2022-07-27)
In droplet-based single-cell RNA-sequencing (scRNA-seq) experiments, cells, along with some of their surrounding buffer and ambient material, are encapsulated into droplets for mRNA capture and barcoding. This protocol details the steps for human gut tissue dissociation using cold active protease
Larry E Tetone et al.
Proceedings of the National Academy of Sciences of the United States of America, 114(7), E1081-E1090 (2017-02-01)
The secondary channel (SC) of multisubunit RNA polymerases (RNAPs) allows access to the active site and is a nexus for the regulation of transcription. Multiple regulatory proteins bind in the SC and reprogram the catalytic activity of RNAP, but the
Timothy T Harden et al.
Nature communications, 11(1), 448-448 (2020-01-25)
RNA polymerases (RNAPs) transcribe genes through a cycle of recruitment to promoter DNA, initiation, elongation, and termination. After termination, RNAP is thought to initiate the next round of transcription by detaching from DNA and rebinding a new promoter. Here we
Larry J Friedman et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(24), 9740-9745 (2013-05-31)
Sequence-specific DNA binding proteins must quickly bind target sequences, despite the enormously larger amount of nontarget DNA present in cells. RNA polymerases (or associated general transcription factors) are hypothesized to reach promoter sequences by facilitated diffusion (FD). In FD, a
Timothy T Harden et al.
Proceedings of the National Academy of Sciences of the United States of America, 113(3), 602-607 (2016-01-07)
Production of a messenger RNA proceeds through sequential stages of transcription initiation and transcript elongation and termination. During each of these stages, RNA polymerase (RNAP) function is regulated by RNAP-associated protein factors. In bacteria, RNAP-associated σ factors are strictly required
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