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Recombinant Human MMP-8 Protein (RP02626LQ)

Recombinant Human MMP-8 Protein was determined by SDS-PAGE with Coomassie Blue, showing a band at 60-75 kDa.

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货号: RP02626LQ
促销价:   ¥950
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详细信息

种属
Human
表达宿主
HEK293 cells
描述
Recombinant Recombinant Human MMP-8 Protein is produced by HEK293 cells expression system. The target protein is expressed with sequence (Phe21-Gly467) of Human MMP-8 (Accession #NP_002415.1) fused with a His tag at the C-terminus.
标签
C-His
纯度
> 90% by SDS-PAGE.
内毒素
< 0.01EU/μg of the protein by LAL method
制剂
Supplied as 0.22 μm filtered solution in50mM Tris , 10 mM CaCl2,150 mM NaCl, (pH 7.5).
储存
Store at ≤-70°C, stable for 12 months after receipt. Store at ≤-70°C, stable for 3 months under sterile conditions after opening. Please minimize freeze-thaw cycles.未开盖的干粉蛋白在 -20°C至-80°C可保存12个月;
复溶之后,蛋白溶液在-20°C及以下可保存3个月,在2-8℃可保存1周。

蛋白复溶计算器

请在蛋白复溶计算器中输入蛋白总质量和所需终浓度,快速计算您需要添加溶液的体积吧!
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背景信息

MMP-8 ,Can degrade fibrillar type I, II, and III collagens.Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases that degrade components of the extracellular matrix (ECM) and play essential roles in various physiological processes such as morphogenesis, differentiation, angiogenesis, and tissue remodeling, as well as pathological processes including inflammation, arthritis, cardiovascular diseases, pulmonary diseases, and tumor invasion. Neutrophil collagenase, also known as Matrix metalloproteinase-8, MMP-8, and CLG1, is a member of the peptidase M1A family. MMP-8 may affect the metastatic behavior of breast cancer cells through protection against lymph node metastasis, underlining the importance of anti-target identification in drug development. MMP-8 in the tumor may have a protective effect against lymph node metastasis. MMP-8 may affect the metastatic behavior of breast cancer cells through protection against lymph node metastasis, underlining the importance of anti-target identification in drug development. MMP-8 participates in wound repair by contributing to the resolution of inflammation and open the possibility to develop new strategies for treating wound healing defects.

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