

Supplier:
Aviva Systems Biology IncorporatedOAT (ornithine aminotransferase (gyrate atrophy)) Blocking Peptide (the middle region of protein) (100ug)
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SPECIFICATIONS
Size
100 ug
Format
Lyophilized powder
Presku
AAP48134
Target
OAT is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. 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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-42 DB459793.1 27-68 43-2062 BC016928.1 1-2020 2063-2066 M12267.1 2010-2013
Weight
45kDa
Gene Id
4942
Alternative Names
DKFZp781A11155; HOGA
Applications
ELISA
Hosts
Mouse
Reactivities
Rat
Applications
ELISA
Hosts
Mouse
Applications
FC
Hosts
Mouse
Reactivities
Hum
Applications
ELISA, WB
Hosts
Mouse
Reactivities
Hum
Applications
ELISA, IHC
Hosts
Mouse
Reactivities
Hum
Applications
ELISA
Hosts
Mouse
Reactivities
Hum
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