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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

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