ALDH1A3 Antibody (Center) Blocking Peptide
€293.00
In stock
SKU
AC-BP7847c
Background:
Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. The enzyme ALDH1A3 uses retinal as a substrate, either in a free or cellular retinol-binding protein form.
Other Names: Aldehyde dehydrogenase family 1 member A3, Aldehyde dehydrogenase 6, Retinaldehyde dehydrogenase 3, RALDH-3, RalDH3, ALDH1A3, ALDH6
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP7847c was selected from the Center region of human ALDH1A3. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Type: Synthetic peptide
Primary Accession: P47895
Gene ID: 220
Gene Name: ALDH1A3
Format: Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
Bio References:
Rexer,B.N., Cancer Res. 61 (19), 7065-7070 (2001)Yoshida,A., Eur. J. Biochem. 251 (3), 549-557 (1998)
Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. The enzyme ALDH1A3 uses retinal as a substrate, either in a free or cellular retinol-binding protein form.
Other Names: Aldehyde dehydrogenase family 1 member A3, Aldehyde dehydrogenase 6, Retinaldehyde dehydrogenase 3, RALDH-3, RalDH3, ALDH1A3, ALDH6
Target/Specificity:
The synthetic peptide sequence used to generate the antibody AP7847c was selected from the Center region of human ALDH1A3. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Type: Synthetic peptide
Primary Accession: P47895
Gene ID: 220
Gene Name: ALDH1A3
Format: Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
Bio References:
Rexer,B.N., Cancer Res. 61 (19), 7065-7070 (2001)Yoshida,A., Eur. J. Biochem. 251 (3), 549-557 (1998)
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