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ALDH3A2 Polyclonal Antibody, Unconjugated
Description
Aldehyde dehydrogenase isozymes are believed to have a significant role in eliminating aldehydes produced during alcohol metabolism and lipid peroxidation. This particular gene product facilitates the conversion of long-chain aliphatic aldehydes into fatty acids. Mutations in this gene result in Sjogren-Larsson syndrome. Additionally, various alternative versions of transcribed variants encoding different forms of this gene have been identified.
Basic Information
Synonyms: | ALDH3A2, Aldh4, Aldh4 r, Aldh4r, Ahd 3, Ahd3, Ahd 3r, AL3A2, Ahd3 r, Aldehyde dehydrogenase 10, Aldehyde dehydrogenase 3 family, Aldehyde dehydrogenase 3, Aldehyde dehydrogenase 3 family, member A2, Aldehyde dehydrogenase family 3 member A2, subfamily A2, Aldehyde dehydrogenase family 3, Aldehyde dehydrogenase, family 3, member 2, subfamily A, Aldh3, ALDH10, DKFZp686E23276, FALDH, Fatty aldehyde dehydrogenase, FLJ20851, Microsomal aldehyde dehydrogenase, msALDH, SLS |
Application: | WB/IHC/ELISA |
Label/Conjugates: | Unconjugated |
Crossreactivity: | Human |
Source/Host: | Rabbit |
Uniprot: | P51648 |
Accession: | BC002430 |
Buffer: | 50% glycerol, PBS with 0.05% sodium azide, PH7.4 |
Concentration: | 0.2 mg/mL |
Isotype: | IgG |
Purification: | Affinity purification |
Immunogen Properties
Abbre: | ALDH3A2 |
Calculated MW: | 55 kDa |
Clonality: | Polyclonal |
Immunogen: | Fusion protein derived from human ALDH3A2 |
Shipping and Handling
Stability & Storage: | Store the sample at a temperature of -20°C and avoid subjecting it to repeated freeze/thaw cycles. |
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