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HSPG2 (基因名), Basement membrane-specific heparan sulfate proteoglycan core protein (蛋白名), pgbm_human.
产品名称:

Human HSPG2/ Basement membrane-specific heparan sulfate proteoglycan core protein Recombinant Protein
硫酸乙酰肝素蛋白聚糖/串珠素

货号:

R0565h

商标:
EIAab®
监管等级:
别名:

Perlecan, PLC, HSPG

序列号:
P98160
来源:
E.coli
种属:
Human
标签:
His
序列:
4120-4391aa
预估分子量:
29.92 kDa (monomer)
纯度:
Greater than 95% 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:
-
Human HSPG2 Protein
规格 & 价格: cart
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Human HSPG2 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
Human HSPG2 Protein
Recombinant human HSPG2 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 1p36.12 by HGNC 1p36.12 by Entrez Gene 1p36.12 by Ensembl
HSPG2 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:
Purified perlecan has a strong tendency to aggregate in dimers or stellate structures. It interacts with other basement membrane components such as laminin, prolargin and collagen type IV. Interacts with COL13A1, FGFBP1 and VWA1. Interacts (via C-terminus) with ECM1 (via C-terminus).


功能:
The LG3 peptide has anti-angiogenic properties that require binding of calcium ions for full activity.


亚细胞位置:
Secreted Extracellular space Extracellular matrix Basement membrane


该产品尚未在任何出版物中被引用。

[1].
"An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and Alzheimer's disease."

[2].
"Cloning of human heparan sulfate proteoglycan core protein, assignment of the gene (HSPG2) to 1p36.1----p35 and identification of a BamHI restriction fragment length polymorphism."

[3].
"No replication of genetic association between candidate polymorphisms and Alzheimer's disease."

[4].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[5].
"A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM)."

[6].
"Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes."

[7].
"The intracranial aneurysm susceptibility genes HSPG2 and CSPG2 are not associated with abdominal aortic aneurysm."

[8].
"Association of the HSPG2 gene with neuroleptic-induced tardive dyskinesia."

[9].
"Role of tyrosine phosphatase SHP-1 in the mechanism of endorepellin angiostatic activity."

[10].
"Preliminary results in a study regarding the relationship between perlecan gene polymorphism and spinal muscular atrophy type I disease."
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