CD105/Endoglin
Cat#: BSH-7631-100, 100ul, BSH-7631-1, 1ml
Alias names: ENG, END, ORW, HHT1, ORW1, CD105, FLJ41744, Optibodies, Optibody
MW: 71kDa
Substrate/Buffer: TRIS with 0.03% sodium azide, pH7,2
Clonality: Mouse monoclonal antibody
Clone: BS71
Application: IHC-P
S/R: Human
Control tissues: Tonsil and appendix
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 TGFB1 and TGFB3 with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as OslerRendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. Endoglin is higly expressed especially in vascular tumor endothelia.
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Endoglin – Tonsil Tonsil section has been stained using endoglin optibody (Clone: BS71) with 1:200 dilution. Endoglin stains vascular endothelia with moderate to strong intensity. |
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Endoglin – Urinary bladder carcinoma Tonsil section has been stained using endoglin optibody (Clone: BS71) with 1:200 dilution. Endoglin stains vascular endothelia with moderate to strong intensity. |
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Endoglin – Ductal breast adenocarcinoma Ductal breast adenocarcinoma section has been stained with endoglin optibody (Clone: BS71) with 1:200 dilution. Vascular endothelia are strongly stained in intratumoral area. |
Price | 1.155,00 RON (preturile sunt fara TVA) | ||||||||||
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Description |
CD105/Endoglin Cat#: BSH-7631-100, 100ul, BSH-7631-1, 1ml Alias names: ENG, END, ORW, HHT1, ORW1, CD105, FLJ41744, Optibodies, Optibody MW: 71kDa Substrate/Buffer: TRIS with 0.03% sodium azide, pH7,2 Clonality: Mouse monoclonal antibody Clone: BS71 Application: IHC-P S/R: Human Control tissues: Tonsil and appendix 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 TGFB1 and TGFB3 with high affinity. Mutations in this gene cause hereditary hemorrhagic telangiectasia, also known as OslerRendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. Endoglin is higly expressed especially in vascular tumor endothelia.
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