Hemoglobin alpha antibody

Synonyms:Alpha globin antibody, HBA1 antibody, HBA2 antibody, Hemoglobin a antibody, Hemoglobin alpha chain antibody, Hemoglobin subunit alpha antibody, hemoglobin antibody, alpha 1 antibody
Catalogue No.:FNab03825Reactivity:Mouse, Rat
Host:RabbitTested Application:ELISA, WB, IHC
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
Hemoglobin alpha antibody
Catalogue No.
FNab03825
Size
100μg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
hemoglobin, alpha 1
Alternative Names
Alpha globin antibody, HBA1 antibody, HBA2 antibody, Hemoglobin a antibody, Hemoglobin alpha chain antibody, Hemoglobin subunit alpha antibody, hemoglobin antibody, alpha 1 antibody
UniProt ID
P69905
Observed MW
13 kDa
Application
Tested Applications
ELISA, WB, IHC
Recommended dilution
WB: 1:500 - 1:2000; IHC: 1:50 - 1:100
Validated Images
mouse liver were subjected to SDS PAGE followed by western blot with FNab03825(Hemoglobin alpha antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded mouse heart using FNab03825(Hemoglobin alpha antibody) at dilution of 1:100
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.