ALDH4A1 antibody

Synonyms:Delta-1-pyrroline-5-carboxylate dehydrogenase antibody, mitochondrial (P5C dehydrogenase)|Aldehyde dehydrogenase family 4 member A1|L-glutamate gamma-semialdehyde dehydrogenase|ALDH4A1|ALDH4|P5CDH antibody
Catalogue No.:FNab00296Reactivity:Human, Mouse
Host:RabbitTested Application:ELISA, WB, IHC
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
ALDH4A1 antibody
Catalogue No.
FNab00296
Size
100μg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
aldehyde dehydrogenase 4 family, member A1
Alternative Names
Delta-1-pyrroline-5-carboxylate dehydrogenase antibody, mitochondrial (P5C dehydrogenase)|Aldehyde dehydrogenase family 4 member A1|L-glutamate gamma-semialdehyde dehydrogenase|ALDH4A1|ALDH4|P5CDH antibody
UniProt ID
P30038
Observed MW
61 kDa
Application
Tested Applications
ELISA, WB, IHC
Recommended dilution
WB: 1:500 - 1:2000; IHC: 1:50 - 1:200
Validated Images
human heart tissue were subjected to SDS PAGE followed by western blot with FNab00296(ALDH4A1 antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded human esophageal cancer using FNab00296(ALDH4A1 antibody) at dilution of 1:100
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.