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HBA1 antibody

This anti-HBA1 antibody is a Rabbit Polyclonal antibody detecting HBA1 in WB, IHC and ELISA. Suitable for Mouse and Rat.
Catalog No. ABIN7114938

Quick Overview for HBA1 antibody (ABIN7114938)

Target

See all HBA1 Antibodies
HBA1 (Hemoglobin, alpha 1 (HBA1))

Reactivity

  • 40
  • 19
  • 3
  • 3
  • 2
Mouse, Rat

Host

  • 45
  • 8
Rabbit

Clonality

  • 43
  • 10
Polyclonal

Conjugate

  • 32
  • 7
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HBA1 antibody is un-conjugated

Application

  • 38
  • 23
  • 16
  • 12
  • 10
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    hemoglobin, alpha 1

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:100

    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

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    Alternative Name

    Hemoglobin alpha

    Background

    Synonyms:Alpha globin, HBA1, HBA2, Hemoglobin a, Hemoglobin alpha chain, Hemoglobin subunit alpha, hemoglobin, alpha 1 Background:The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported.

    Molecular Weight

    13 kDa

    Gene ID

    3040

    UniProt

    P69905
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