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HGD
Homogentisate 1,2-dioxygenaseAKU, HGO
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]
Top validated antibodies |
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| Boster Biological Technology |  A01909-1 |
Polyclonal |
WB
EL
ICC
IHC
FC
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| Invitrogen Antibodies | H00003081-M09 |
Monoclonal |
EL
ICC
IP
OA
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| Biorbyt | orb412976 |
Polyclonal |
WB
EL
ICC
IHC
FC
|
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| Atlas Antibodies | HPA052359 |
1 references | Polyclonal |
WB
ICC
IHC
|
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| antibodies-online | ABIN396085 |
5 references | Monoclonal |
EL
ICC
|
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