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Biological source:
bovine
Form:
liquid
Technique(s):
ELISA: suitable, PCR: suitable, immunoblotting: suitable
Impurities:
≤0.02% Fatty acids, ≤10 ppm Heavy metal, ≤2.0% Ash
Concentration:
1 g/10 mL (Aqueous Solution)
Servicio técnico
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Permítanos ayudarleNombre del producto
Albumin, Bovine Serum, 10% Aqueous Solution,
biological source
bovine
Quality Level
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
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
Disclaimer
Toxicity: Standard Handling (A)
Clase de almacenamiento
12 - Non Combustible Liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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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 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
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