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Endoglin antibody (AA 380-409)

The Rabbit Polyclonal anti-Endoglin antibody is suitable to detect Endoglin in samples from Human and Mouse. It has been validated for WB, FACS and IHC (p).
Catalog No. ABIN389408
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$383.35
$451.00
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Quick Overview for Endoglin antibody (AA 380-409) (ABIN389408)

Target

See all Endoglin (ENG) Antibodies
Endoglin (ENG)

Reactivity

  • 239
  • 71
  • 70
  • 21
  • 17
  • 16
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  • 3
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  • 1
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Human, Mouse

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 7
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  • 2
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  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
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  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
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This Endoglin antibody is un-conjugated

Application

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Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB17987
  • Binding Specificity

    • 16
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    • 8
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    • 1
    • 1
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    AA 380-409

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This CD105 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 380-409 amino acids from the Central region of human CD105.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. IHC-P: 1:10~50. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • 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.

    Molecular Weight

    70578

    Gene ID

    2022

    NCBI Accession

    NP_000109, NP_001108225, NP_001265067

    UniProt

    P17813
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