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FIGURE: 1 / 5
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total HFE.
The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin. It is thought that this protein functions to regulate iron absorption by regulating the interaction of the transferrin receptor with transferrin. The iron storage disorder, hereditary haemochromatosis, is a recessive genetic disorder that results from defects in this gene. At least nine alternatively spliced variants have been described for this gene. Additional variants have been found but their full-length nature has not been determined.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: hemochromatosis; hereditary hemochromatosis protein HLA-H; HFE 1; high Fe; HLA H; MGC10379; MGC103790; MGC:150812; MHC class I-like protein HFE; RT1-CAFE; unnamed protein product
Gene Aliases: HFE1; HH; HLA-H; MR2; MVCD7; TFQTL2
UniProt ID: (Human) Q30201, (Rat) O35799, (Mouse) P70387
Entrez Gene ID: (Human) 3077, (Rat) 29199, (Mouse) 15216
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