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COMP/TSP5 human

品牌
Sigma-Aldrich
货号
SRP6457
规格纯度
recombinant, expressed in HEK 293 cells, ≥95% (SDS-PAGE)
参考价格
3563.77 *本价格含增值税费
促销
服务
  • 原厂保证
  • 包邮
  • 增值税票
数量
-+
产品名称:
COMP/TSP5 human
EPD1
PSACH
EDM1
THBS5
MED
产品介绍:

产品说明

一般描述

Cartilage oligomeric matrix protein (COMP) also known as Thrombospondin-5 (TSP5), EDM1, EPD1, MED, PSACH, THBS5, which belongs to the thrombospondin family. COMP / TSP5 contain 4 EGF-like domains, 1 TSP C-terminal (TSPC) domain, 8 TSP type-3 repeats. Abundantly expressed in the chondrocyte extracellular matrix, and is also found in bone, tendon, ligament and synovium and blood vessels. COMP may play a role in the structural integrity of cartilage via its interaction with other extracellular matrix proteins such as the collagens and fibronectin. COMP can mediate the interaction of chondrocytes with the cartilage extracellular matrix through interaction with cell surface integrin receptors. Thrombospondin-5 could play a role in the pathogenesis of osteoarthritis. COMP is a marker of cartilage turnover.
Cartilage oligomeric matrix protein (COMP), also known as thrombospondin 5 (TSP5), is a key constituent of the extracellular matrix of the musculoskeletal system. It is encoded by the gene mapped to human chromosome 19p13.11. COMP/TSP5 is a fifth member of TSP family. It is a pentameric protein, characterized with an N-terminal coiled- coil oligomerization domain, four type II (EGF-like) domains, eight type III calmodulin like repeats (CLR) and a C-terminal globular domain (CTD).

生化/生理作用

Cartilage oligomeric matrix protein (COMP) plays a vital role in chondrocyte attachment, differentiation and cartilage extracellular matrix assembly. COMP levels vary in cartilage of osteoarthritis and rheumatoid arthritis patients compared with healthy individuals. Thus, COMP levels in serum and synovial fluid can be used as a biomarker for these diseases. Polymorphism in the gene leads to the development of two autosomal dominant skeletal dysplasias named, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia type 1 (MED1).

外形

Lyophilized from 0.22 μm filtered solution in 50 mM Tris, 100 mM NaCl, pH 7.5. Normally Mannitol or Trehalose is added as protectants before lyophilization.

重悬

Centrifuge the vial prior to opening. Reconstitute in sterile PBS, pH 7.4 to a concentration of 50 μg/mL. Do not vortex. This solution can be stored at 2-8℃ for up to 1 month. For extended storage, it is recommended to store at -20℃.

基本信息

NACRESNA.32

产品性质

生物来源human
重组expressed in HEK 293 cells
标签6-His tagged (C-terminus)
测定≥95% (SDS-PAGE)
形式lyophilized
效能1 μg
分子量calculated mol wt 82 kDa
observed mol wt 110-130 kDa (DTT-reduced. Protein migrates due to glycosylation. Gln 21 is the predicted N-terminal.)
包装pkg of 10 and 50 μg
杂质<1 EU/μg endotoxin (LAL test)
UniProt登记号P49747
运输wet ice
储存温度−20℃
Gene Informationhuman ... COMP(1311)

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable

Sigma-Aldrich

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