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aHSP antibody

This Rabbit Polyclonal antibody specifically detects aHSP in WB, IF (p) and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN1387096

Quick Overview for aHSP antibody (ABIN1387096)

Target

See all aHSP Antibodies
aHSP (alpha Hemoglobin Stabilizing Protein (aHSP))

Reactivity

  • 42
  • 8
  • 3
Human

Host

  • 42
  • 9
Rabbit

Clonality

  • 43
  • 8
Polyclonal

Conjugate

  • 24
  • 5
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This aHSP antibody is un-conjugated

Application

  • 42
  • 24
  • 14
  • 12
  • 11
  • 6
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Cross-Reactivity

    Human

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human AHSP/ERAF

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    4 °C,-20 °C

    Storage Comment

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    Expiry Date

    12 months
  • Target

    aHSP (alpha Hemoglobin Stabilizing Protein (aHSP))

    Alternative Name

    AHSP

    Background

    Synonyms: AHSP, AHSP_HUMAN, Alpha hemoglobin stabilizing protein, Alpha-hemoglobin-stabilizing protein, EDRF, ERAF, Erythroid associated factor, Erythroid dferentiation associated factor, Erythroid dferentiation related factor, Erythroid dferentiation-related factor, Erythroid-associated factor.

    Background: Act as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation. It is predicted to modulate pathological states of alpha-hemoglobin excess such as beta-thalassemia.

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