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HBA1 antibody

This anti-HBA1 antibody is a Rabbit Monoclonal antibody detecting HBA1 in WB, IHC and IF. Suitable for Human.
Catalog No. ABIN7267608

Quick Overview for HBA1 antibody (ABIN7267608)

Target

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

Reactivity

  • 39
  • 20
  • 4
  • 3
  • 2
Human

Host

  • 45
  • 8
Rabbit

Clonality

  • 44
  • 9
Monoclonal

Conjugate

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

Application

  • 38
  • 23
  • 17
  • 12
  • 10
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purpose

    Hemoglobin subunit alpha (HBA1) Rabbit mAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human Hemoglobin subunit alpha (HBA1) (HBA1)

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    Alternative Name

    HBA1

    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. [provided by RefSeq, Jul 2008],HBA-T3, HBH,HBA1

    Molecular Weight

    15kDa

    Gene ID

    3039

    UniProt

    P69905
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