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Merck
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RECOMT

凝血酶 CleanCleave 试剂盒

别名:

Thrombin Cleavage Kit

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关于此项目

NACRES:
NA.56
UNSPSC Code:
12352200
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form

suspension

mol wt

37 kDa

technique(s)

protein purification: suitable

shipped in

wet ice

storage temp.

2-8°C

Quality Level

General description

凝血酶 CleanCleave 试剂盒包含通过固定牛凝血酶产生的 50% 凝血酶 - 琼脂糖悬浮液,用于切割重组融合蛋白

Application

用于从含有凝血酶识别序列的重组融合蛋白切割标签。凝血酶 - 琼脂糖与在各种类型的表达系统中表达的重组蛋白相容。

Features and Benefits

  • 在短短 2 小时内快速、有效地裂解
  • 凝血酶与琼脂糖共价结合,易于除去。
  • 在 4°C 到 37°C 的温度范围内,以及在广泛的 pH 和离子强度范围内,强裂解反应是有效的。
  • 即使在 0.1%Triton,1M 尿素或 5mM EDTA 存在下,也能裂解标签
  • 凝血酶 - 琼脂糖是可重复使用的

Preparation Note

200 μl 50% 的凝血酶 - 琼脂糖浆液裂解 >85% 的 1mg 融合蛋白。

Legal Information

CleanCleave is a trademark of Sigma-Aldrich Co. LLC
Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

仅试剂盒组分

产品编号
说明

  • Thrombin Cleavage Buffer, 10× 10 mL

存储类别

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

常规特殊物品
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历史批次信息供参考:

分析证书(COA)

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Anna-Maj Albertsson et al.
Journal of neuroinflammation, 11, 197-197 (2014-12-04)
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The Journal of biological chemistry, 279(50), 51981-51988 (2004-10-07)
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Manish Gupta et al.
Frontiers in microbiology, 7, 886-886 (2016-07-06)
Mycobacterium tuberculosis H37Rv escapes host-generated stresses by entering a dormant persistent state. Activation of toxin-antitoxin modules is one of the mechanisms known to trigger such a state with low metabolic activity. M. tuberculosis harbors a large number of TA systems
Ohad Fisher et al.
Nucleic acids research, 32(1), 287-297 (2004-01-13)
The DNA methylation status of the protozoan parasite Entamoeba histolytica was heretofore unknown. In the present study, we developed a new technique, based on the affinity of methylated DNA to 5-methylcytosine antibodies, to identify methylated DNA in this parasite. Ribosomal
Pertti Koivisto et al.
The Journal of biological chemistry, 278(45), 44348-44354 (2003-08-29)
The Escherichia coli AlkB protein, and two human homologs ABH2 and ABH3, directly demethylate 1-methyladenine and 3-methylcytosine in DNA. They couple Fe(II)-dependent oxidative demethylation of these damaged bases to decarboxylation of alpha-ketoglutarate. Here, we have determined the kinetic parameters for

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实验方案

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