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CD105 (ABT-CD105) Mouse mAb

-YM4391

Catalog: YM4391
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

40μL
$190.00
In stock

0

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Main Information
Target

CD105(Endoglin)

Host Species

Mouse

Reactivity

Human,

Applications

IHC, WB, IF, ELISA

MW

70kD (Calculated)

75kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
IHC 1:200-1000; WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000
Formulation
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Specificity
The antibody can specifically recognize human CD105 protein.
Purification
Protein G
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
MW(Calculated)
70kD
MW(Observed)
75kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
ABT-CD105
Isotype
IgG2a,Kappa
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human CD105(Endoglin) AA range: 400-500
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Specificity:
The antibody can specifically recognize human CD105 protein.
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Gene Name:
ENG END
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Protein Name:
Endoglin (CD antigen CD105)
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Other Name:
AI528660 ;
AI662476 ;
CD 105 ;
CD105 ;
CD105 antigen ;
EGLN_HUMAN ;
END ;
Endoglin ;
Eng ;
FLJ41744 ;
HHT1 ;
ORW ;
ORW1 ;
Osler Rendu Weber syndrome 1 ;
RP11 228B15.2 ;
S endoglin ;
S-endoglin ;
SN6
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Database Link:
Organism Gene ID SwissProt
Human 2022; P17813;
Background:
CD105 is a homodimeric cell membrane glycoprotein linked by disulfide bonds. It is a new class of cell adhesion molecules and plays an important role in regulating angiogenesis. As a receptor of TGF-beta, CD105 is highly expressed in vascular endothelial cells of tumor related neovascular endothelium. Therefore, the evaluation of tumor microvessel density by immunohistochemical staining is significantly correlated with tumor invasion and prognosis.
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Function:
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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Cellular Localization:
Cytoplasmic
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Tissue Expression:
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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Catalog: YM4391
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

40μL
$190.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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