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TIMP4 (基因名), Metalloproteinase inhibitor 4 (蛋白名), timp4_human.
产品名称:

Human TIMP4/ Metalloproteinase inhibitor 4 Recombinant Protein
金属蛋白酶抑制剂4

货号:

R0130h

商标:
EIAab®
监管等级:
别名:

Tissue inhibitor of metalloproteinases 4, TIMP-4

序列号:
Q99727
来源:
E.coli
种属:
Human
标签:
His
序列:
30-224aa
预估分子量:
21.45 kDa (monomer)
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Cardiovascular
Human TIMP4 Protein
规格 & 价格: cart
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Human TIMP4 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 3p25.2 by HGNC 3p25.2 by Entrez Gene 3p25.2 by Ensembl
TIMP4 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
N/A


功能:
Complexes with metalloproteinases (such as collagenases) and irreversibly inactivates them by binding to their catalytic zinc cofactor. Known to act on MMP-1, MMP-2, MMP-3, MMP-7 and MMP-9.


亚细胞位置:
Secreted


该产品尚未在任何出版物中被引用。

[1].
"Cloning of the human tissue inhibitor of metalloproteinase-4 gene (TIMP4) and localization of the TIMP4 and Timp4 genes to human chromosome 3p25 and mouse chromosome 6, respectively."

[2].
"Molecular cloning and characterization of human tissue inhibitor of metalloproteinase 4."

[3].
"Promoter polymorphism (rs3755724, -55C/T) of tissue inhibitor of metalloproteinase 4 (TIMP4) as a risk factor for Kawasaki disease with coronary artery lesions in a Korean population."

[4].
"Polymorphisms of MMP-3 and TIMP-4 genes affect angiographic coronary plaque progression in non-diabetic and type 2 diabetic patients."

[5].
"Association of TIMP-4 gene polymorphism with the risk of osteoarthritis in the Korean population."

[6].
"Maternal and fetal genetic associations of PTGER3 and PON1 with preterm birth."

[7].
"Interferon gamma receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection."

[8].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[9].
"Spontaneous preterm birth in African Americans is associated with infection and inflammatory response gene variants."

[10].
"Racial disparity in pathophysiologic pathways of preterm birth based on genetic variants."
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