推荐产品
产品名称
Albumin, Bovine Serum, 10% Aqueous Solution, Nuclease-Free,
生物来源
bovine
质量水平
描述
Merck USA index - 14, 8468
表单
liquid
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
浓度
0.1 g/10 mL (Aqueous Solution)
技术
ELISA: suitable
PCR: suitable
immunoblotting: suitable
杂质
≤0.02% Fatty acids
≤10 ppm Heavy metal
≤2.0% Ash
异质活性
Nuclease, none detected
Protease, none detected
运输
ambient
储存温度
2-8°C
一般描述
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.
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.
警告
Toxicity: Standard Handling (A)
外形
10% aqueous solution, 0.22 µm-filtered, pH 6.8-7.2.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
储存分类代码
12 - Non Combustible Liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
监管及禁止进口产品
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
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
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
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