Description
ALAS2 Polyclonal Antibody | E-AB-10763 | Gentaur UK, US & Europe Distribution
Type: Polyclonal Antibody
Synonyms: 5 @aminolevulinate synthase erythroid specific, 5 aminolevulinate synthase 2, 5 aminolevulinate synthase 5 aminolevulinate synthase 2, 5 aminolevulinate synthase erythroid specific mitochondrial, 5 aminolevulinic acid synthase 2, 5 aminolevulinic acid synthase, 5-aminolevulinate synthase, 5-aminolevulinic acid synthase 2, Alas 2, ALAS, ALAS E, ALAS, erythroid, ALAS-E, Alas2, ALASE, Aminolevulinate delta synthase 2, Aminolevulinic acid synthase 2, erythroid, ANH1, ASB, Delta ALA synthase 2, Delta ALA synthetase, Delta aminolevulinate synthase 2, Delta aminolevulinate synthase, Delta-ALA synthase 2, Delta-aminolevulinate synthase 2, Erythroid specific ALAS, erythroid-specific, FLJ93603, HEM0, mitochondrial, OTTHUMP00000023388, OTTHUMP00000023389, OTTMUSP00000020679, RP23-338A17.1, SIDBA1, XLDPP, XLEPP, XLSA
Application: WB, ELISA
Reactivity: Human, Mouse, Rat
Host: Rabbit
Isotype: IgG
Reserch Areas: Cancer, Cardiovascular, Metabolism, Signal Transduction
Background: The product of this gene specifies an erythroid-specific mitochondrially located enzyme. The encoded protein catalyzes the first step in the heme biosynthetic pathway. Defects in this gene cause X-linked pyridoxine-responsive sideroblastic anemia. Alternatively spliced transcript variants encoding different isoforms have been identified.
Concentration: 0.2 mg/mL
Storage: Store at -20°C. Avoid freeze / thaw cycles.
Immunogen: Recombinant protein of human ALAS2
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification Method: Affinity purification
Dilution: WB 1:500-1:2000
Clone: N/A
Conjugation: Unconjugated
Molecular Weight(Calculated): 64 kDa
Molecular Weight(Observed): N/A