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CD105 (ABT-CD105) mouse mAb (Ready to Use)

-YM6570R

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Catalog: YM6570R
Size
Price
Status
Qty.
10mL
$240.00
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6mL
$180.00
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3mL
$120.00
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Main Information
Target

CD105(Endoglin)

Host Species

Mouse

Reactivity

Human,

Applications

IHC

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
Ready to use for IHC
Formulation
The prediluted ready-to-use antibody is diluted in phosphate buffer saline containing stabilizing protein and 0.05% Proclin 300
Specificity
The antibody can specifically recognize human CD105 protein.
Purification
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
Storage
2°C to 8°C/1 year
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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Database Link:
Organism Gene ID SwissProt
Human 2022; P17813;
Background:
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],
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: YM6570R
Size
Price
Status
Qty.
10mL
$240.00
In stock

0

6mL
$180.00
In stock

0

3mL
$120.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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