- Tel: 858.663.9055
- Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
The ACAA1 gene encodes an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of 3-ketoacyl-CoA thiolase (peroxisomal) leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants.
Titration of the ACAA1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.
A portion of amino acids 147-176 from the human protein was used as the immunogen for this ACAA1 antibody.
Aliquot the ACAA1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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