CD105 (ENG) (NM_000118) Human Recombinant Protein
Product Specifications
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]
Synonyms
END; HHT1; ORW1
Gene ID
2022
UniProt
P17813, Q5T9B9
Accession Number mRNA
NM_000118
Chromosomal Location
9q34.11
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome, ES Cell Differentiation/IPS, Transmembrane
Molecular Weight
65 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
ENG
Species
Human
Protein ID
NP_000109
Overview
Recombinant protein of human endoglin (ENG), transcript variant 2
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/2022
Uniprot URL
https://www.uniprot.org/uniprot/P17813
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_000118
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_000109
Curated Selection
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