- Poly28640 (See other available formats)
- Other Names
- Hemoglobin Subunit Alpha 1, Hemoglobin Alpha 1, HBA2
- Rabbit Polyclonal IgG
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- Product Citations
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HBα1 (Hemoglobin alpha 1) is a component of the complex that forms hemoglobin in the red blood cells, which carries and transports oxygen to the peripheral tissues. Deletions of HBα1 lead to a genetic disorder called alpha thalassemia, a blood disorder in which hemoglobin production is reduced.Product Details
- Antibody Type
- Host Species
- Recombinant HBα1 (Met1~Arg142) with N-terminal His-Tag
- 0.01 M PBS, pH7.4, containing 0.02% NaN3, 50% glycerol.
- The antibody was purified by affinity chromatography.
- 0.5 mg/ml
- Storage & Handling
- Store at 4°C for up to 3 months. For longer term storage aliquot into small volumes and store at -20°C.
WB - Quality tested
- Recommended Usage
Each lot of this antibody is quality control tested by Western blotting. For Western blotting, the suggested use of this reagent is 0.05 - 1.0 µg per ml. It is recommended that the reagent be titrated for optimal performance for each application.
- HBα1 is a 142 amino acid protein with predicted and observed molecular mass of ~15 kD.
Tissue Distribution: Bone marrow and spleen
Cellular Distribution: Extracellular and cytosol
- HBα1 is a component of the hemoglobin complex that carries oxygen.
- HBα1 forms heterotetramer with HBβ1.
- Biology Area
- Molecular Family
- Blood Group Markers, Carrier Proteins
- Antigen References
- Patrinos GP, et al. 2005. Hum Mutat. 26(5):399
- Standing SJ, et al. 1992. Ann Clin Biochem. 29:494
- Koslowski H, et al. 1990. Padiatr Grenzgeb. 29(1):25
- Gene ID
- 3039 View all products for this Gene ID 3040 View all products for this Gene ID
- View information about HBalpha1 on UniProt.org
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