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CD105 (ABT-CD105) mouse mAb

-YM6570

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货号: YM6570
规格
价格
货期
数量
200μL
¥3,780.00
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100μL
¥2,300.00
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40μL
¥960.00
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主要信息
Target

CD105(Endoglin)

Host Species

Mouse

Reactivity

Human,

Applications

IHC, ELISA

MW

70kD (Calculated)

75kD (Observed)

Conjugate/Modification

Unmodified

详细信息
推荐稀释比
IHC 1:50-200; ELISA 1:500-5000
组成
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
特异性
The antibody can specifically recognize human CD105 protein.
纯化工艺
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
理论分子量
70kD
实测条带
75kD
修饰
Unmodified
克隆性
Monoclonal
克隆号
ABT-CD105
同种型
IgG2a,Kappa
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抗原&靶点信息
免疫原:
Synthesized peptide derived from human CD105(Endoglin) AA range: 400-500
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特异性:
The antibody can specifically recognize human CD105 protein.
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基因名称:
ENG END
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蛋白名称:
Endoglin (CD antigen CD105)
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数据库链接:
Organism 基因 ID SwissProt
Human 2022; P17813;
背景:
This gene encodes a homodimeric transmembrane protein which is a major glycoprotein of the vascular endothelium. This protein is a component of the transforming growth factor beta receptor complex and it binds to the beta1 and beta3 peptides with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. This gene may also be involved in preeclampsia and several types of cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2013],
功能:
Disease:Defects in ENG are the cause of hereditary hemorrhagic telangiectasia type 1 (HHT1) [MIM:187300, 108010]; also known as Osler-Rendu-Weber syndrome 1 (ORW1). HHT1 is an autosomal dominant multisystemic vascular dysplasia, characterized by recurrent epistaxis, muco-cutaneous telangiectases, gastro-intestinal hemorrhage, and pulmonary (PAVM), cerebral (CAVM) and hepatic arteriovenous malformations; all secondary manifestations of the underlying vascular dysplasia. Although the first symptom of HHT1 in children is generally nose bleed, there is an important clinical heterogeneity.,Function:Major glycoprotein of vascular endothelium. May play a critical role in the binding of endothelial cells to integrins and/or other RGD receptors.,subunit:Homodimer that forms an heteromeric complex with the signaling receptors for transforming growth factor-beta: TGF-beta receptors I and/or II. It is able to bind TGF-beta 1, and 3 efficiently and TGF-beta 2 less efficiently. Interacts with TCTEX1D4.,tissue specificity:Endoglin is restricted to endothelial cells in all tissues except bone marrow.,
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细胞定位:
Cytoplasmic
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组织表达:
Detected on umbilical veil endothelial cells (PubMed:10625079). Detected in placenta (at protein level) (PubMed:1692830). Detected on endothelial cells (PubMed:1692830).
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货号: YM6570
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询

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