CD105 (ENG) Mouse Monoclonal Antibody (Biotin conjugated) [Clone ID: OTI8A1]

CAT#: TA506170AM

ENG mouse monoclonal antibody,clone 8A1, Biotinylated

Product Images

Immunofluorescent staining of HeLa cells using anti-ENG mouse monoclonal antibody (TA506170).

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  HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY ENG (RC221699, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-ENG. Positive lysates LY424919 (100ug) and LC424919 (20ug) can be purchased separately from OriGene.

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  Western blot analysis of extracts (35ug) from 9 different cell lines by using anti-ENG monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: human; MDCK: canine; PC12: rat; MCF7: human).

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  Western blot analysis of extracts (10ug) from a mouse cell line and 3 different mouse tissues by using anti-ENG monoclonal antibody (1:200).

Specifications

Product Data

• Clone Name: OTI8A1
• Applications: IF, WB
• Recommended Dilution: WB 1:200~4000, IF 1:100
• Reactivities: Human, Monkey, Mouse, Rat, Dog
• Host: Mouse
• Isotype: IgG2b
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human ENG(NP_000109) produced in HEK293T cell.
• Concentration: 0.5 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Biotin
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 65 kDa
• Gene Name: endoglin
• Database Link:
  NP_000109
  Entrez Gene 13805 MouseEntrez Gene 497010 RatEntrez Gene 609166 DogEntrez Gene 706569 MonkeyEntrez Gene 2022 Human
  UniProt ID P17813
• 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. [provided by RefSeq, Sep 2008]
• Synonyms: END; HHT1; ORW1

Reference Data

• Protein Families: Druggable Genome, ES Cell Differentiation/IPS, Transmembrane