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HGD Products

Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26.
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16 results for "HGD" in Products

16 results for "HGD" in Products

HGD Products

Homogentisate 1,2-dioxygenase (HGD) gene mutations are the molecular cause of alkaptonuria, a rare hereditary disorder of the phenylalanine catabolism. The highest expression of HGD is in the prostate, small intestine, colon, and liver. The HGD gene contains 14 exons. Conflicting reports have placed the gene at 3q2, 3q13.3-q21, 3q21-q24, 3q21-q23, or 3q25-q26.
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Applications: IHC, WB, ICC/IF
Reactivity: Human
Applications: IHC, WB
Reactivity: Human
Applications: IHC, WB, ICC/IF
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: WB, ELISA, IP
Reactivity: Human
Applications: ELISA, ICC/IF
Reactivity: Human
Applications: IHC, ELISA
Reactivity: Human

Recombinant monoclonal antibody expressed in HEK293F cells

Applications: ELISA
Applications: WB
Reactivity: Human
Catalog #: H00003081-T01
Applications: WB
Catalog #: H00003081-Q01
Applications: WB, ELISA, MA, AP
Applications: WB, ELISA, MA, AP, PAGE
Applications: WB, ELISA, MA, AP, PAGE
Applications: WB
Reactivity: Human

Recombinant Monoclonal Antibody

Applications: ELISA
Applications: AC
Applications: AC
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