Homogentisate 1,2-dioxygenase Antibody / HGD
The HGD gene encodes homogentisate 1,2-dioxygenase (HGD), an enzyme involved in the catabolism of phenylalanine and tyrosine. 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 is mapped to chromosome 3q21-q23 by a preliminary PCR screen of hamster/human somatic cell hybrid genomic DNA samples and by fluorescence in situ hybridization.
Product Specifications
CAS Number
9007-83-4
Specifications
Western blot: 0.5-1 µg/mL, Immunohistochemistry (FFPE) : 2-5 µg/mL, Flow cytometry: 1-3ug/million cells
UniProt
Q93099
Host
Mouse
Reactivity
Human
Immunogen
Recombinant human protein (amino acids D374-N445) was used as the immunogen for the Homogentisate 1,2-dioxygenase antibody.
Clonality
Monoclonal
Isotype
IgG2b
Clone
2F11E1
Applications
WB, IHC-P, FACS
Purity
Antigen affinity purified
Format
Antigen affinity purified
Buffer
Lyophilized from 1X PBS with 2% Trehalose
Reconstitution
Limitations
This Homogentisate 1,2-dioxygenase antibody is available for research use only.
Storage Conditions
Formulation
0.5 mg/mL if reconstituted with 0.2ml sterile DI water
Applications Notes
Optimal dilution of the Homogentisate 1,2-dioxygenase antibody should be determined by the researcher.
Location
Cytoplasmic
Image Legend
Documents
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