推荐产品
产品名称
Albumin, Bovine Serum, 10% Aqueous Solution, Nuclease-Free,
生物源
bovine
品質等級
描述
Merck USA index - 14, 8468
形狀
liquid
製造商/商標名
Calbiochem®
儲存條件
OK to freeze
濃度
0.1 g/10 mL (Aqueous Solution)
技術
ELISA: suitable
PCR: suitable
immunoblotting: suitable
雜質
≤0.02% Fatty acids
≤10 ppm Heavy metal
≤2.0% Ash
異物活動
Nuclease, none detected
Protease, none detected
運輸包裝
ambient
儲存溫度
2-8°C
一般說明
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.
警告
Toxicity: Standard Handling (A)
外觀
10% aqueous solution, 0.22 µm-filtered, pH 6.8-7.2.
法律資訊
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
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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
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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
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