HGD rabbit pAb
Ref. EK-ES15769
50µl | 188.00 € | ||
100µl | 316.00 € |
Product Information
This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.[provided by RefSeq, May 2010],
Chemical properties
Technical inquiry about: EK-ES15769 HGD rabbit pAb
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