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HMHA1 antibody

This anti-HMHA1 antibody is a Rabbit Polyclonal antibody detecting HMHA1 in WB, ELISA and IHC. Suitable for Human, Rat and Mouse.
Catalog No. ABIN7115031

Quick Overview for HMHA1 antibody (ABIN7115031)

Target

See all HMHA1 Antibodies
HMHA1 (Histocompatibility (Minor) HA-1 (HMHA1))

Reactivity

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  • 4
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  • 1
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  • 1
Human, Rat, Mouse

Host

  • 24
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Rabbit

Clonality

  • 26
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Polyclonal

Conjugate

  • 15
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  • 1
  • 1
  • 1
  • 1
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This HMHA1 antibody is un-conjugated

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    histocompatibility(minor) HA-1

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:2000, IHC: 1:20-1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    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

    -20 °C

    Storage Comment

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    HMHA1 (Histocompatibility (Minor) HA-1 (HMHA1))

    Alternative Name

    HMHA1

    Background

    Synonyms:KIAA0223 Background:GTPase activator for the Rho-type GTPases. Precursor of the histocompatibility antigen HA-1. More generally, minor histocompatibility antigens(mHags) refer to immunogenic peptide which, when complexed with MHC, can generate an immune response after recognition by specific T-cells. The peptides are derived from polymorphic intracellular proteins, which are cleaved by normal pathways of antigen processing. The binding of these peptides to MHC class I or class II molecules and its expression on the cell surface can stimulate T-cell responses and thereby trigger graft rejection or graft-versus-host disease(GVHD) after hematopoietic stem cell transplantation from HLA-identical sibling donor. GVHD is a frequent complication after bone marrow transplantation(BMT), due to mismatch of minor histocompatibility antigen in HLA-matched sibling marrow transplants. Specifically, mismatching for mHag HA-1 which is recognized as immunodominant, is shown to be associated with the development of severe GVHD after HLA-identical BMT. HA-1 is presented to the cell surface by MHC class I HLA-A*0201, but also by other HLA-A alleles. This complex specifically elicits donor-cytotoxic T-lymphocyte(CTL) reactivity against hematologic malignancies after treatment by HLA-identical allogenic BMT. It induces cell recognition and lysis by CTL.

    Molecular Weight

    140-150kd

    Gene ID

    23526

    UniProt

    Q92619
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