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Merck
CN

M6542

Sigma-Aldrich

Macrophage Inflammatory Protein-1β from mouse

recombinant, expressed in E. coli, lyophilized powder, suitable for cell culture

别名:

mMIP-1β, MIP-1β

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MDL编号:
UNSPSC代码:
12352202
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生物来源

mouse

重组

expressed in E. coli

方案

≥97% (SDS-PAGE and N-terminal analysis)

表单

lyophilized powder

效能

40-100 ng/mL ED50/EC50

分子量

7.8 kDa

包装

pkg of 10 μg

储存条件

avoid repeated freeze/thaw cycles

技术

cell culture | mammalian: suitable

杂质

endotoxin, tested

UniProt登记号

储存温度

−20°C

基因信息

mouse ... Ccl4(20303)

一般描述

MIP-1α and MIP-1β (macrophage inflammatory protein) were originally co-purified from LPS stimulated mouse macrophages. Recombinant, mouse MIP-1β (rmMIP-1β) consists of 69 amino acids. MIP- 1β belongs to the chemokine β subfamily which is characterized by a C-C configuration at the first two cysteines. MIP-1β has endogenous pyrogenic activity when it is injected intravenously into rabbits. Although other cytokines, such as IL-1alpha, IL-1β and TNF have endogenous pyrogenic activity, the pyrogenic effects of these cytokines can be inhibited by cyclooxgenase blockers, while the pyrogenicity of MIP- 1β is unaffected by these agents. MIP-1β can synergize with the hematopoietic growth factors granulocyte macrophage CSF (GM-CSF) or macrophage CSF (M-CSF) to enhance colony formation.

生化/生理作用

MIP-1β has endogenous pyrogenic activity when it is injected intravenously into rabbits. MIP-1 can synergize with the hematopoietic growth factors granulocytemacrophage CSF (GM-CSF) or macrophage CSF (M-CSF) to enhance colony formation.

外形

Lyophilized from a 0.2 μm filtered solution in 30% acetonitrile and 0.1% trifluoroacetic acid containing 0.5 mg bovine serum albumin

分析说明

The biological activity of MIP-1β was tested in culture by measuring its ability to inhibit hematopoietic stem cell proliferation in an in vitro colony assay.

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G J Graham et al.
Nature, 344(6265), 442-444 (1990-03-29)
The haemopoietic system has three main compartments: multi-potential stem cells, intermediate stage progenitor cells and mature cells. The availability of simple reproducible culture systems has made possible the characterization and purification of regulators of the progenitor cells, including colony-stimulating factors

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