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IHC-P analysis of rat spleen tissue section using Hemoglobin alpha [GT1234] Hemoglobin alpha [GT1234]. Dilution : 1:100 Blue : DAPI for nuclear staining.
IHC-P analysis of rat spleen tissue section using Hemoglobin alpha [GT1234] Hemoglobin alpha [GT1234]. Dilution : 1:100 Blue : DAPI for nuclear staining.
IHC-P analysis of rat spleen tissue section using Hemoglobin alpha [GT1234] Hemoglobin alpha [GT1234]. Dilution : 1:100 Blue : DAPI for nuclear staining.

Hemoglobin alpha antibody [GT1234]

GTX02831
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetHBA1
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Overview

  • Supplier
    GeneTex
  • Product Name
    Hemoglobin alpha antibody [GT1234]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. IHC-P: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    GT1234
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID3039
  • Target name
    HBA1
  • Target description
    hemoglobin subunit alpha 1
  • Target synonyms
    alpha globin chain; alpha one globin; alpha-2 globin chain; delta globin; ECYT7; HBA-T3; HBH; hemoglobin alpha 1 globin chain; hemoglobin subunit alpha; hemoglobin, alpha 1; METHBA
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP69905
  • Protein Name
    Hemoglobin subunit alpha
  • Scientific Description
    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]
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352203

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