AL4A1 rabbit pAb
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AL4A1 rabbit pAb
Background :
This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2009]Description :
This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jun 2009],Product Name Alternative :
Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial (P5C dehydrogenase) (EC 1.5.1.12) (Aldehyde dehydrogenase family 4 member A1)UniProt :
P30038Swiss Prot :
P30038Reactivity :
Human; Mouse; RatImmunogen :
Synthesized peptide derived from human AL4A1 AA range: 39-89Target :
AL4A1Clonality :
PolyclonalSource :
RabbitApplications :
WBConcentration :
1 mg/mlDilution :
WB 1:500-2000Buffer :
-20°C/1 yearMolecular Weight :
60kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
60kDFragment :
IgGSubcellular Location :
Mitochondrion matrix.Other Product Names :
Delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial (P5C dehydrogenase) (EC 1.5.1.12) (Aldehyde dehydrogenase family 4 member A1)Gene ID (Human) :
8659

