AASS 产品
(Aminoadipate Semialdehyde Synthase (AASS))
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This gene encodes a bifunctional enzyme that catalyzes the first two steps in the mammalian lysine degradation pathway. The N-terminal and the C-terminal portions of this enzyme contain lysine-ketoglutarate reductase and saccharopine dehydrogenase activity, respectively, resulting in the conversion of lysine to alpha-aminoadipic semialdehyde. Mutations in this gene are associated with familial hyperlysinemia. [provided by RefSeq, Jul 2008].
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Recommended AASS 抗体
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Reactivity
Application
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Datasheet
Reactivity
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Cat. No.
ABIN7444178
Quantity
100 μL
Datasheet
Datasheet
Reactivity
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Cat. No.
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Quantity
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Datasheet
Datasheet
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Cat. No.
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Recommended AASS 蛋白
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Source
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Cat. No.
ABIN7417786
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Mouse
Source
Escherichia coli (E. coli)
Validations
Cat. No.
ABIN7417861
Quantity
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Datasheet
Datasheet
Latest Publications for our AASS Products
: "Genetic basis of hyperlysinemia." in: Orphanet journal of rare diseases, Vol. 8, pp. 57, (2013) (PubMed).Synonyms and alternative names related to AASS
aminoadipate-semialdehyde synthase (AASS), aminoadipate-semialdehyde synthase (Aass), LKR, LKR/SDH, LKRSDH, LOR, LOR/SDH, LORSDH, Lorsdh, SDHProtein level used designations for AASS
- alpha-aminoadipate semialdehyde synthase
- alpha-aminoadipic semialdehyde synthase, mitochondrial
- aminoadipic semialdehyde synthase
- lysine-2-oxoglutarate reductase
- lysine-ketoglutarate reductase /saccharopine dehydrogenase
- lysine oxoglutarate reductase
- saccharopine dehydrogenase
- LKR/SDH
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