8 results for "HGD Antibodies" in 产品

HGD Antibodies

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.

Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: IHC, WB, ICC/IF
Western Blot: HGD Antibody [NBP2-49039]
(10)
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Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: IHC, WB
Western Blot: HGD Antibody [NBP2-33488]
(9)
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Reactivity: Human
Details: Mouse IgG2a Kappa Monoclonal Clone #1F1
Applications: WB, ELISA, IP
Western Blot: HGD Antibody (1F1) [H00003081-M11]
(3)
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Recombinant Monoclonal Antibody

Reactivity: Human
Details: Rabbit IgG Monoclonal Clone #SR1835
Applications: IHC, WB, ICC/IF
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Recombinant Monoclonal Antibody

Reactivity: Human
Details: Rabbit IgG Monoclonal Clone #20D12
Applications: IHC, ELISA
HGD Antibody (20D12)
(2)
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Reactivity: Human
Details: Mouse IgG2b Kappa Monoclonal Clone #3G4
Applications: ELISA, ICC/IF
Immunocytochemistry/ Immunofluorescence: HGD Antibody (3G4) [H00003081-M10]
(2)
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Reactivity: Human
Details: Rabbit IgG Polyclonal
Applications: WB
Western Blot: HGD Antibody [NBP1-55134]
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Recombinant Monoclonal Antibody

Reactivity: Human
Details: Rabbit IgG Monoclonal Clone #7O8Q1
Applications: WB
Western Blot: HGD Antibody (7O8Q1) [NBP3-15477]
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