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HGD, Mouse, Clone: 1F1, Abnova™
Mouse monoclonal antibody raised against a full-length recombinant HGD.
Supplier: Abnova Corporation H00003081M11
Description
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. [provided by RefSeq
Sequence: MAELKYISGFGNECSSEDPRCPGSLPEGQNNPQVCPYNLYAEQLSGSAFTCPRSTNKRSWLYRILPSVSHKPFESIDEGHVTHNWDEVDPDPNQLRWKPFEIPKASQKKVDFVSGLHTLCGAGDIKSNNGLAIHIFLCNTSMENRCFYNSDGDFLIVPQKGNLLIYTEFGKMLVQPNEICVIQRGMRFSIDVFEETRGYILEVYGVHLELPDLGPIGANGLANPRDFLIPIAWYEDRQVPGGYTVINKYQGKLFAAKQDVSPFNVVAWHGNYTPYKYNLKNFMVINSVAFDHADPSIFTVLTALRRPARSSWHLRGLPMAPWHLCLNHLSpecifications
HGD | |
Monoclonal | |
Unconjugated | |
PBS with no preservative; pH 7.4 | |
BC020792 | |
HGD | |
HGD (AAH20792, 1 a.a. ∼ 329 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. | |
100 μg | |
Primary | |
Human | |
Antibody | |
IgG2a κ |
ELISA, Immunoprecipitation, Western Blot | |
1F1 | |
Mouse monoclonal antibody raised against a full-length recombinant HGD. | |
HGD | |
AKU/HGO | |
Mouse | |
Affinity chromatography | |
RUO | |
3081 | |
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. | |
Liquid |
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