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- Tel: 858.663.9055
- Email: info@nsjbio.com
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The HMBS gene encodes a member of the hydroxymethylbilane synthase superfamily. The encoded protein is the third enzyme of the heme biosynthetic pathway and catalyzes the head to tail condensation of four porphobilinogen molecules into the linear hydroxymethylbilane. Mutations in this gene are associated with the autosomal dominant disease acute intermittent porphyria. [RefSeq]
Optimal dilution of the HMBS antibody should be determined by the researcher.
A synthetic peptide specific to human HMBS was used as the immunogen for the HMBS antibody.
Store the HMBS antibody at -20oC.
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