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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.
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.
| Cat.No | ADA-09024A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | HBA2 |
| Target Synonyms | HBH; ECYT7; HBA-T2; HBA2 | Form | Liquid |
| Species Reactivity | Human, Mouse, Rat | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | Mouse liver | Application | ELISA, WB, IF/ICC |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 1-142 of human HBA2 (NP_000508.1). | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | MVLSPADKTNVKAAWGKVGAHAGEYGAEALERMFLSFPTTKTYFPHFDLSHGSAQVKGHGKKVADALTNAVAHVDDMPNALSALSDLHAHKLRVDPVNFKLLSHCLLVTLAAHLPAEFTPAVHASLDKFLASVSTVLTSKYR | Uniprot ID | P69905 |
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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