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  2. Monoclonal

GTX40079

Hemoglobin antibody [901]

Cannot supply to this region.

SKU:
GTX40079
Additional Names:
CD31 Antibody , HBA1 Antibody , HBH Antibody
Application:
ELISA
Concentration:
1.1 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Protein G Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Mouse
Reactivities:
Human
Buffer:
PBS, no preservatives.
Immunogen:
Full length native protein (purified) (Human)
Clone:
901
Synonyms:
alpha globin chain;alpha one globin;alpha-2 globin chain;delta globin;ECYT7;HBA-T3;HBH;hemoglobin alpha 1 globin chain;hemoglobin subunit alpha;hemoglobin, alpha 1;METHBA
Extra Details:
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]
Shipping Conditions:
Blue Ice