Endoglin antibody
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- Target See all Endoglin (ENG) Antibodies
- Endoglin (ENG)
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Reactivity
- Human
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Host
- Mouse
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Clonality
- Monoclonal
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Conjugate
- This Endoglin antibody is un-conjugated
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Application
- Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (IHC), ELISA, Immunocytochemistry (ICC)
- Purification
- purified
- Immunogen
- Purified recombinant fragment of human CD105 expressed in E. coli.
- Clone
- 3A9
- Isotype
- IgG1
- Top Product
- Discover our top product ENG Primary Antibody
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- Application Notes
- ELISA: 1:10000, WB: 1:500 - 1:2000, IHC: 1:200 - 1:1000, ICC: 1:200 - 1:1000, FCM: 1:200 - 1:400
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Ascitic fluid containing 0.03 % sodium azide.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- 4 °C/-20 °C
- Storage Comment
- 4°C, -20°C for long term storage
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Endoglin (CD105) expression in the human heart throughout gestation: an immunohistochemical study." in: Reproductive sciences (Thousand Oaks, Calif.), Vol. 15, Issue 10, pp. 1018-26, (2008) (PubMed).
: "Endoglin (CD105) as a urinary and serum marker of prostate cancer." in: International journal of cancer. Journal international du cancer, Vol. 124, Issue 3, pp. 664-9, (2008) (PubMed).
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Endoglin (CD105) expression in the human heart throughout gestation: an immunohistochemical study." in: Reproductive sciences (Thousand Oaks, Calif.), Vol. 15, Issue 10, pp. 1018-26, (2008) (PubMed).
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- Target
- Endoglin (ENG)
- Alternative Name
- CD105 (ENG Products)
- Synonyms
- ENG antibody, MGC137842 antibody, DKFZp469D0419 antibody, END antibody, HHT1 antibody, ORW1 antibody, AI528660 antibody, AI662476 antibody, CD105 antibody, S-endoglin antibody, endoglin antibody, ENG antibody, Eng antibody
- Background
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Description: 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.
Aliases: ENG, END, ORW, HHT1, ORW1, CD105, FLJ41744
- Molecular Weight
- 71 kDa
- Gene ID
- 2022
- HGNC
- 2022
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