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IHC-P analysis of human spleen tissue using GTX04752 Hemoglobin alpha antibody [EGI-8].
IHC-P analysis of human spleen tissue using GTX04752 Hemoglobin alpha antibody [EGI-8].
IHC-P analysis of human spleen tissue using GTX04752 Hemoglobin alpha antibody [EGI-8].

Hemoglobin alpha antibody [EGI-8]

GTX04752
GeneTex
ApplicationsFlow Cytometry, ImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetHBA1
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Overview

  • Supplier
    GeneTex
  • Product Name
    Hemoglobin alpha antibody [EGI-8]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:2000. IHC-P: 1:50-1:200. FCM: 1:50. IP: 1:50. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Flow Cytometry, ImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    EGI-8
  • Conjugate
    Unconjugated
  • Gene ID3039
  • Target name
    HBA1
  • Target description
    hemoglobin subunit alpha 1
  • Target synonyms
    ECYT7, HBA-T3, HBH, METHBA, hemoglobin subunit alpha, alpha globin chain, alpha one globin, alpha-2 globin chain, delta globin, hemoglobin alpha 1 globin chain, hemoglobin, alpha 1
  • 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]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    41116161