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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
IDI1 encodes a peroxisomally-localized enzyme that catalyzes the interconversion of isopentenyl diphosphate (IPP) to its highly electrophilic isomer, dimethylallyl diphosphate (DMAPP), which are the substrates for the successive reaction that results in the synthesis of farnesyl diphosphate and, ultimately, cholesterol. It has been shown in peroxisomal deficiency diseases such as Zellweger syndrome and neonatal adrenoleukodystrophy that there is reduction in IPP isomerase activity.
Optimal dilution of the IDI1 antibody should be determined by the researcher.
An E.coli-derived human recombinant protein (amino acids M1-M227) was used as the immunogen for the IDI1 antibody.
After reconstitution, the IDI1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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