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Endoglin antibody (AA 380-409)

This anti-Endoglin antibody is a Rabbit Polyclonal antibody detecting Endoglin in WB, FACS, IHC and ELISA. Suitable for Human and Mouse.
Catalog No. ABIN3030354

Quick Overview for Endoglin antibody (AA 380-409) (ABIN3030354)

Target

See all Endoglin (ENG) Antibodies
Endoglin (ENG)

Reactivity

  • 209
  • 72
  • 65
  • 20
  • 19
  • 16
  • 15
  • 3
  • 3
  • 3
  • 2
  • 1
Human, Mouse

Host

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  • 112
  • 16
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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 15
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  • 2
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Endoglin antibody is un-conjugated

Application

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  • 85
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Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (IHC), ELISA
  • Binding Specificity

    • 16
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    AA 380-409

    Purification

    Purified

    Immunogen

    A portion of amino acids 380-409 from the human protein was used as the immunogen for this CD105 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the CD105 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:10-1:50,Flow Cytometry: 1:10-1:50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % 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

    -20 °C

    Storage Comment

    Aliquot the CD105 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    Endoglin (ENG)

    Alternative Name

    CD105

    Background

    CD105 is 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 its gene cause hereditary hemorrhagic telangiectasia, also known as Osler-Rendu-Weber syndrome 1, an autosomal dominant multisystemic vascular dysplasia.

    UniProt

    P17813
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