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Endoglin antibody (Middle Region)

The Rabbit Polyclonal anti-Endoglin antibody has been validated for WB and EIA. It is suitable to detect Endoglin in samples from Human.
Catalog No. ABIN951149

Quick Overview for Endoglin antibody (Middle Region) (ABIN951149)

Target

See all Endoglin (ENG) Antibodies
Endoglin (ENG)

Reactivity

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

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 1
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  • 1
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This Endoglin antibody is un-conjugated

Application

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Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 16
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    AA 272-302, Middle Region

    Specificity

    This antibody recognizes Human CD105 / Endoglin (Center).

    Purification

    Affinity Chromatography on Protein A

    Immunogen

    KLH conjugated synthetic peptide between 272-302 amino acids from the Central region of Human CD105 / Endoglin. Genename: ENG

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    PBS containing 0.09 % (W/V) Sodium Azide as preservative

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    Endoglin (ENG)

    Alternative Name

    CD105 / Endoglin

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

    Molecular Weight

    70578 Da

    Gene ID

    2022

    NCBI Accession

    NP_000109
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