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HBA1

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.
Protein class

Disease related genes, FDA approved drug targets, Human disease related genes, Plasma proteins, Transporters

Predicted location

Intracellular

Single cell type specificity

Cell type enriched (Erythroid cells)

Immune cell specificity

Immune cell enhanced (neutrophil, plasmacytoid DC)

Cell line specificity

Group enriched (HEL, K-562)

Interaction

Heterotetramer of two alpha chains and two beta chains in adult hemoglobin A (HbA); two alpha chains and two delta chains in adult hemoglobin A2 (HbA2); two alpha chains and two epsilon chains in early embryonic hemoglobin Gower-2; two alpha chains and two gamma chains in fetal hemoglobin F (HbF). (Microbial infection) Interacts with Staphylococcus aureus protein isdB.

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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