ENG antibody (clone 4C11), anti-human
€435.00
In stock
SKU
AC-AT1907a
Catalog Number: AC-AT1907a
Size: 100 µg
Isotype: mouse IgG1 Kappa
Applications: WB, IP, E
Request Information AC-AT1907a">Request Information
Size: 100 µg
Isotype: mouse IgG1 Kappa
Applications: WB, IP, E
Request Information AC-AT1907a">Request Information
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 TGFB1 and TGFB3 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. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Other Names:
Endoglin, CD105, ENG, END
Antigen Type:
Recombinant Protein
Gene Name: ENG
Gene ID: 2022
NCBI Accession: NP_000109.1;NP_001108225.1;NP_001265067.1
Primary Accession: P17813
Other Accession: BC014271
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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 Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Other Names:
Endoglin, CD105, ENG, END
Antigen Type:
Recombinant Protein
Gene Name: ENG
Gene ID: 2022
NCBI Accession: NP_000109.1;NP_001108225.1;NP_001265067.1
Primary Accession: P17813
Other Accession: BC014271
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
| Is Featured? | No |
|---|
Write Your Own Review