OAT purified MaxPab rabbit polyclonal antibody (D01P)
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More Files
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human OAT protein.
Immunogen
OAT (NP_000265.1, 1 a.a. ~ 439 a.a) full-length human protein.
Sequence
MFSKLAHFQRFAVLSRGVHSSVASATSVATKKTVQGPPTSDDIFEREYKYGAHNYHPLPVALERGKGIYLWDVEGRKYFDFLSSYSAVNQGHCHPKIVNALKSQVDKLTLTSRAFYNNVLGEYEEYITKLFNYHKVLPMNTGVEAGETACKLARKWGYTVKGIQKYKAKIVFAAGNFWGRTLSAISSSTDPTSYDGFGPFMPGFDIIPYNDLPALERALQDPNVAAFMVEPIQGEAGVVVPDPGYLMGVRELCTRHQVLFIADEIQTGLARTGRWLAVDYENVRPDIVLLGKALSGGLYPVSAVLCDDDIMLTIKPGEHGSTYGGNPLGCRVAIAALEVLEEENLAENADKLGIILRNELMKLPSDVVTAVRGKGLLNAIVIKETKDWDAWKVCLRLRDNGLLAKPTHGDIIRFAPPLVIKEDELRESIEIINKTILSF
Host
Rabbit
Reactivity
Human
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of OAT expression in transfected 293T cell line (H00004942-T02) by OAT MaxPab polyclonal antibody.
Lane 1: OAT transfected lysate(48.50 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — OAT
Entrez GeneID
4942GeneBank Accession#
NM_000274.1Protein Accession#
NP_000265.1Gene Name
OAT
Gene Alias
DKFZp781A11155, HOGA
Gene Description
ornithine aminotransferase (gyrate atrophy)
Omim ID
258870Gene Ontology
HyperlinkGene Summary
This gene encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme is 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. [provided by RefSeq
Other Designations
OTTHUMP00000020690|ornithine aminotransferase
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Interactome
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Pathway
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Disease
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