别名:DKFZp781A11155; GACR; gyrate atrophy; HOGA; OAT应用:WB
反应种属:Human,Mouse,Rat
规格:50μl/100μl
| Description |
|---|
| This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Alternatively spliced transcript variants encoding different isoforms have been described. Related pseudogenes have been defined on the X chromosome.ana G., Proc. Natl. Acad. Sci. U.S.A. 83:1203-1207(1986).Ramesh V., DNA 5:493-501(1986). |
| Specification | |
|---|---|
| Aliases | DKFZp781A11155; GACR; gyrate atrophy; HOGA; OAT |
| Entrez GeneID | 4942; |
| Swissprot | P04181 |
| WB Predicted band size | 49kDa |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human,Mouse,Rat |
| Immunogen | Synthesized peptide derived from Internal of human OAT. |
| Formulation | Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. |
| Application | |
|---|---|
| WB | 1/500-1/3000 |
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Western blot analysis of extracts from K562/COLO205 cells, using OAT antibody P42509. |
本公司的所有产品仅用于科学研究或者工业应用等非医疗目的,不可用于人类或动物的临床诊断或治疗,非药用,非食用。
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本公司的所有产品仅用于科学研究或者工业应用等非医疗目的,不可用于人类或动物的临床诊断或治疗,非药用,非食用。
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