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Endoglin antibody (Middle Region)

The Rabbit Polyclonal anti-Endoglin antibody is suitable to detect Endoglin in samples from Human. It has been validated for WB and EIA.
Catalog No. ABIN951149
$768.00
Plus shipping costs $50.00
0.4 mL
Shipping to: United States
Delivery in 1 to 2 Business Days

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

Target

See all Endoglin (ENG) Antibodies
Endoglin (ENG)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This Endoglin antibody is un-conjugated

Application

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

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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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