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SMOC2 Rabbit pAb (bs-7506R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價
產品編號 bs-7506R
英文名稱 SMOC2 Rabbit pAb
中文名稱 分泌模塊化鈣結合蛋白2/平滑肌相關蛋白2抗體
別    名 Secreted modular calcium binding protein 2; SMAP 2; SMAP2; SMOC 2; Smooth muscle associated protein 2; SPARC related modular calcium binding 2; dJ421D16.1; MST117; MSTP117; bA270C4A.1; bA37D8.1; dJ421D16.1(novel thyroglobulin type 1 repeat containing protein); MSTP140; SMOC2_HUMAN.  
Specific References  (1)     |     bs-7506R has been referenced in 1 publications.
[IF=4.147] Feng Long. et al. A SMOC2 variant inhibits BMP signaling by competitively binding to BMPR1B and causes growth plate defects. Bone. 2021 Jan;142:115686  WB ;  Human.  
研究領域 心血管  細胞生物  信號轉導  生長因子和激素  轉錄調節因子  血管內皮細胞  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Dog)
產品應用 ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 47 kDa
檢測分子量
細胞定位 細胞膜 細胞外基質 分泌型蛋白 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SMOC2: 311-410/446 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 SMOC 2 (Secreted modular calcium binding protein 2) is a secreted modular protein containing an EF hand calcium binding domain homologous to that in BM40. It consists of two thyroglobulin like domains, a follistatin like domain and a novel domain found only in the homologous SMOC 1. SMOC 1 and 2 form a separate group within the BM40 family. SMOC 2 is a glycoprotein with a calcium dependent conformation. SMOC 2 contains 2 EF hand calcium binding domains, 1 Kazal like domain and 2 thyroglobulin type I domains.

Function:
Promotes matrix assembly and cell adhesiveness. Can stimulate endothelial cell proliferation, migration, as well as angiogenesis.

Subunit:
Binds various proteins from the extracellular matrix.

Subcellular Location:
Secreted, extracellular space, extracellular matrix, basement membrane.

DISEASE:
Defects in SMOC2 are the cause of dentin dysplasia typ1 (DTDP1) [MIM:125400]. A dental defect in which both primary and secondary dentitions are affected. The clinical crowns of both permanent and deciduous teeth are of normal shape, form and color in most cases, although they may be slightly opalescent and blue or brown. Teeth may be very mobile and exfoliate spontaneously because of inadequate root formation. On radiographs, the roots are short and may be more pointed than normal. Pulp chambers are usually absent except for a chevron-shaped remnant in the crown. Root canals are usually absent.

Similarity:
Contains 2 EF-hand domains.
Contains 1 Kazal-like domain.
Contains 2 thyroglobulin type-1 domains.

SWISS:
Q9H3U7

Gene ID:
64094

Database links:

Entrez Gene: 64094 Human

Entrez Gene: 64074 Mouse

Omim: 607223 Human

SwissProt: Q9H3U7 Human

SwissProt: Q8CD91 Mouse

Unigene: 487200 Human

Unigene: 30162 Mouse



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