Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Endoglin antibody

This anti-Endoglin antibody is a Mouse Monoclonal antibody detecting Endoglin in WB, FACS, IHC, ELISA and IF. Suitable for Human.
Catalog No. ABIN865407

Quick Overview for Endoglin antibody (ABIN865407)

Target

See all Endoglin (ENG) Antibodies
Endoglin (ENG)

Reactivity

  • 231
  • 71
  • 70
  • 21
  • 17
  • 16
  • 15
  • 3
  • 3
  • 3
  • 1
  • 1
Human

Host

  • 146
  • 116
  • 20
  • 2
  • 1
  • 1
Mouse

Clonality

  • 163
  • 122
  • 1
Monoclonal

Conjugate

  • 115
  • 29
  • 28
  • 23
  • 18
  • 7
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Endoglin antibody is un-conjugated

Application

  • 165
  • 164
  • 93
  • 55
  • 37
  • 35
  • 27
  • 25
  • 25
  • 18
  • 13
  • 10
  • 7
  • 6
  • 5
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Clone

3A9
  • Purification

    Ascitic fluid

    Immunogen

    Purified recombinant fragment of human CD105 expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    WB: 1/500 - 1/2000, IHC: 1/200 - 1/1000, IF: 1/200 - 1/1000, FC: 1/200 - 1/400, ELISA: Propose dilution 1/10000.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    100g/100l

    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
  • Target

    Endoglin (ENG)

    Alternative Name

    CD105

    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. Synonyms: ENG, END, ORW, HHT1, ORW1, CD105, FLJ41744

    Molecular Weight

    71kDa

    Gene ID

    2022
You are here:
Chat with us!