HFE
hemochromatosis
HFE1, HH, HLA-H, MVCD7, TFQTL2
Human HFE (3077), Mouse Hfe (15216), Rat Hfe (29199), naked mole-rat Hfe (101705145), dog HFE (100688951), domestic cat HFE (101084960), sheep HFE (101105539), cow HFE (497622)
- Human(3077) Summary: The protein encoded by this gene is a membrane protein that is similar to MHC class I-type proteins and associates with beta2-microglobulin (beta2M). 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. [provided by RefSeq, Jul 2008]
- Mouse(15216) hemochromatosis
- Rat(29199) hemochromatosis
- naked mole-rat(101705145) hemochromatosis
- dog(100688951) hemochromatosis
- domestic cat(101084960) hemochromatosis
- sheep(101105539) hemochromatosis
- cow(497622) hemochromatosis
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Antibodies
Anti-HFE antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
human
immunohistochemistry
western blot
western blot
Monoclonal Anti-HFE antibody produced in mouse, clone 1G12, purified immunoglobulin, buffered aqueous solution,
human
ELISA
immunofluorescence
western blot
immunofluorescence
western blot
Anti-HFE antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
human
immunohistochemistry
western blot
western blot