HBA2 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-62782
Catalog Number: E-AB-62782
Isotype: Rabbit IgG
Reactivity: mouse, rat
Applications: IHC
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: mouse, rat
Applications: IHC
Datasheet, Questions? Contact us!
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.
Research Area: Cancer, Cardiovascular
Synonyms:
HBA2, HBA-T2, HBH
Immunogen: Recombinant fusion protein of human HBA2 (NP_000508.1).
Swissprot: P69905
Gene ID: 3040
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "IHC 1:50-1:100"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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.
Research Area: Cancer, Cardiovascular
Synonyms:
HBA2, HBA-T2, HBH
Immunogen: Recombinant fusion protein of human HBA2 (NP_000508.1).
Swissprot: P69905
Gene ID: 3040
Purification Method: Affinity purification
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
Concentration: 1 mg/mL
Dilution: "IHC 1:50-1:100"
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
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