Anti-HGD Polyclonal Antibody, 20.0ul
£72.56
Delivery: 2 weeks
SKU
K111794P-20.0ul
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.
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.
- Size: 20.0ul
- Molecular Weight: 50kDa
- Physical State: Liquid
- Storage: Store at -20℃. Avoid freeze/thaw cycles.
- Application: IHC;WB
- Brand: Saint Michael
- Catalogue No.: K111794P-20.0ul
For laboratory research use only. Not for human or animal consumption, diagnostic or therapeutic use.
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