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Merck
CN

16-156

蛋白A琼脂糖，快流量

Protein A Agarose, Fast Flow suitable for medium and low-pressure chromatography, immunoprecipitation and antibody purification.

别名:

Protein A resin

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关于此项目

UNSPSC Code:
41116133
NACRES:
NA.56
eCl@ss:
32160801

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form

liquid

manufacturer/tradename

Upstate®

technique(s)

affinity chromatography: suitable, immunoprecipitation (IP): suitable, western blot: suitable

shipped in

wet ice

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General description

蛋白质A是一种免疫球蛋白(Ig)结合蛋白，用于纯化大量IgG。它与抗体的Fc部分在CH2–CH3界面结合。蛋白质A-琼脂糖可用于低压抗体分离。
重组蛋白A，共价结合到高度交叉链接的6%琼脂糖磁珠。

结合量 40mg 人 IgG/ml 琼脂糖

Application

蛋白A琼脂糖，Fast Flow已被用于免疫沉淀和染色质免疫沉淀(ChIP)。

Physical form

含有 0.01％ 硫柳汞的无菌蒸馏水

Analysis Note

在免疫沉淀中进行了常规评估

Legal Information

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

Disclaimer

对于美国客户：产品含汞，切勿丢弃于普通垃圾中，请根据当地、州或联邦法规进行处理。

存储类别

10 - Combustible liquids

wgk

WGK 1

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Simon Schenk et al.
American journal of physiology. Endocrinology and metabolism, 291(2), E254-E260 (2006-05-04)
Although the increase in fatty acid oxidation after endurance exercise training has been linked with improvements in insulin sensitivity and overall metabolic health, the mechanisms responsible for increasing fatty acid oxidation after exercise training are not completely understood. The primary
Ghia M Euskirchen et al.
Genome research, 17(6), 898-909 (2007-06-15)
Recent progress in mapping transcription factor (TF) binding regions can largely be credited to chromatin immunoprecipitation (ChIP) technologies. We compared strategies for mapping TF binding regions in mammalian cells using two different ChIP schemes: ChIP with DNA microarray analysis (ChIP-chip)
Lei Jiang et al.
Investigative ophthalmology & visual science, 61(5), 41-41 (2020-05-24)
To identify the pathogenic gene of infantile nystagmus syndrome (INS) in three Chinese families and explore the potential pathogenic mechanism of FERM domain-containing 7 (FRMD7) mutations. Genetic testing was performed via Sanger sequencing. Western blotting was used to analyze protein
Vasavi Sundaram et al.
Genome research, 24(12), 1963-1976 (2014-10-17)
Transposable elements (TEs) have been shown to contain functional binding sites for certain transcription factors (TFs). However, the extent to which TEs contribute to the evolution of TF binding sites is not well known. We comprehensively mapped binding sites for
Yong Cheng et al.
Nature, 515(7527), 371-375 (2014-11-21)
To broaden our understanding of the evolution of gene regulation mechanisms, we generated occupancy profiles for 34 orthologous transcription factors (TFs) in human-mouse erythroid progenitor, lymphoblast and embryonic stem-cell lines. By combining the genome-wide transcription factor occupancy repertoires, associated epigenetic
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