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Rabbit anti-Human HBA2 Polyclonal Antibody

The antibody against HBA2 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-142 of human HBA2 (NP_000508.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

ADA-09024A

The antibody against HBA2 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-142 of human HBA2 (NP_000508.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

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Specifications


Cat.No ADA-09024A ClonalityPolyclonal
Host SpeciesRabbitTarget NameHBA2
Target SynonymsHBH; ECYT7; HBA-T2; HBA2FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesMouse liverApplicationELISA, WB, IF/ICC

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 1-142 of human HBA2 (NP_000508.1).Target SpeciesHuman
Immunogen SequenceMVLSPADKTNVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHGKKVADALTNAVAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTPAVHASLDKFLASVSTVLTSKYRUniprot IDP69905
Background Information
  • Uniprot Id

    P69905

  • Target Species

    Human

  • Target Name

    HBA1

  • Target Full Name

    Hemoglobin subunit alpha

  • Target Function

    Involved in oxygen transport from the lung to the various peripheral tissues.

  • Target Involvement

    Heinz body anemias (HEIBAN); Alpha-thalassemia (A-THAL); Hemoglobin H disease (HBH)

  • Target Protein Families

    Globin family

  • Target Tissue Specificity

    Red blood cells.

  • Target Synonyms

    HBH; ECYT7; HBA-T3; METHBA; Hemoglobin subunit alpha (HBA1)

  • Target 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.

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