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Endoglin antibody (AA 265-294)

This Rabbit Polyclonal antibody specifically detects Endoglin in WB and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN655186

Quick Overview for Endoglin antibody (AA 265-294) (ABIN655186)

Target

See all Endoglin (ENG) Antibodies
Endoglin (ENG)

Reactivity

  • 209
  • 72
  • 66
  • 20
  • 19
  • 16
  • 15
  • 3
  • 3
  • 3
  • 2
  • 1
Human

Host

  • 132
  • 112
  • 16
  • 3
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  • 1
Rabbit

Clonality

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  • 1
Polyclonal

Conjugate

  • 118
  • 30
  • 27
  • 23
  • 15
  • 7
  • 2
  • 2
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  • 2
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  • 2
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  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Endoglin antibody is un-conjugated

Application

  • 156
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  • 18
  • 13
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  • 2
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  • 1
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  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

RB20948
  • Binding Specificity

    • 16
    • 16
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    • 11
    • 11
    • 11
    • 6
    • 4
    • 4
    • 4
    • 4
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    • 1
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    • 1
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    • 1
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    • 1
    • 1
    • 1
    • 1
    • 1
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    • 1
    • 1
    AA 265-294

    Purification

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

    Immunogen

    This ENG antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 265-294 amino acids from the Central region of human ENG.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. 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

    ENG

    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.

    Molecular Weight

    70578

    Gene ID

    2022

    NCBI Accession

    NP_000109, NP_001108225, NP_001265067

    UniProt

    P17813
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