ALDH3A2 Antibody (C-term) Blocking Peptide
€363.00
In stock
SKU
AC-BP1468b
Background:
Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. ALDH3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the ALDH3A2 gene cause Sjogren-Larsson syndrome.
Other Names:
Fatty aldehyde dehydrogenase, Aldehyde dehydrogenase 10, Aldehyde dehydrogenase family 3 member A2, Microsomal aldehyde dehydrogenase, ALDH3A2, ALDH10, FALDH
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP1468b was selected from the C-term region of human ALDH3A2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: ALDH3A2
Gene ID: 224
Primary Accession: P51648
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. ALDH3A2 catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the ALDH3A2 gene cause Sjogren-Larsson syndrome.
Other Names:
Fatty aldehyde dehydrogenase, Aldehyde dehydrogenase 10, Aldehyde dehydrogenase family 3 member A2, Microsomal aldehyde dehydrogenase, ALDH3A2, ALDH10, FALDH
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP1468b was selected from the C-term region of human ALDH3A2. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Gene Name: ALDH3A2
Gene ID: 224
Primary Accession: P51648
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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