Endoglin rabbit pAb

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],

Endoglin (CD antigen CD105)

2022

P17813

Cell membrane ; Single-pass type I membrane protein.

Rabbit

Human,Rat,Mouse,

Synthetic peptide from human protein at AA range: 370-430

Polyclonal

WB,IHC,IF,ELISA

1 year

1 mg/mL

WB 1:500-2000,IHC-p 1:500-200, ELISA 1:10000-20000

70kD

PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.