Anti-Human ALDH3A2 Polyclonal Antibody

Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA07484
Size 100μl
Host Type Rabbit
Immunogen Fusion protein of human ALDH3A2
Specificity
Isotype IgG
Reacitivity Human
Clone
Uniprot P51648
Concentration 0.2 mg/mL
Dilution WB 1:500-2000, IHC 1:25-100, ELISA 1:2000-5000
Formulation
Application WB,IHC,ELISA
Other Names Ahd 3,Ahd 3r,Ahd3,Ahd3 r,AL3A2,Aldehyde dehydrogenase 10,Aldehyde dehydrogenase 3,Aldehyde dehydrogenase 3 family,member A2,Aldehyde dehydrogenase family 3 member A2,Aldehyde dehydrogenase family 3,subfamily A2,Aldehyde dehydrogenase,family 3,subfamily A,member 2,ALDH10,Aldh3,ALDH3A2,Aldh4,Aldh4 r,Aldh4r,DKFZp686E23276,FALDH,Fatty aldehyde dehydrogenase,FLJ20851,Microsomal aldehyde dehydrogenase,msALDH,SLS
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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