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Hemoglobin alpha Antibody

Hemoglobin alpha Antibody

Cat no: 251337

Supplier: ABBIOTEC
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Hemoglobin alpha is involved in o, Xenopus/Amphibian,ygen transport from the lung to the various peripheral tissues. Defects in hemoglobin alpha are the cause of alpha-thalassemia (A-THAL). The thalassemias are the most common monogenic diseases and occur mostly in Mediterranean and Southeast Asian populations. The hallmark of alpha-thalassemia is an imbalance in globin-chain production in the adult HbA molecule. The level of alpha chain production can range from none to very nearly normal levels. Untreated,Mouse,ost patients die in childhood or early adolescence.
Catalogue number: 251337
Reactivities: Human, Mouse, Bovine, Chicken/Bird, Rabbit
Applications: Immunohistochemistry
Size: 0.1 mg
Accession: P69905
Antigen: KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human hemoglobin alpha.
Format: Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4 with 0.09% sodium azide. Antibody was purified by Protein-G affinity chromatography.
P type: Rabbit Polyclonal Antibody
Isotype: Rabbit Ig
Additional info: HBA1; Hemoglobin alpha; Hemoglobin alpha 1; Hemoglobin subunit alpha; Hemoglobin alpha chain; Alpha-globin; HBA1
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