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Your search for "hfe" returned 71 TaqMan® Gene Expression Assays
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]
HFE, HFE1, HH, HLA-H, MR2, MVCD7, TFQTL2
(Human) Q30201, (Human) B2CKL0, (Human) O75929, (Human) O75930, (Human) O75931, (Human) Q17RT0, (Human) Q96KU5, (Human) Q96KU6, (Human) Q96KU7, (Human) Q96KU8, (Human) Q9HC64, (Human) Q9HC68, (Human) Q9HC70, (Human) Q9HC83, (Mouse) P70387, (Mouse) Q14AQ5, (Mouse) Q5SZ90, (Mouse) Q9D754, (Rat) O35799, (Rat) O35175
|Protocol||Protocol: TaqMan® Gene Expression Assays||PDF, 2349.1 KB|
|App Note||Application Note: TaqMan® Gene Expression Assays Endogenous Controls||PDF, 493.8 KB|
|QRC||QRC: TaqMan® Gene Expression Assays||PDF, 200.9 KB|
|White Paper||Design Process for Gene Expression Assays||PDF, 943.6 KB|
|White Paper||Gene Expression Assay Performance Guarantee||PDF, 481.9 KB|
|White Paper||TaqMan® Assays shipped at ambient temperature retain their quality and stability||PDF, 3255.7 KB|
|Brochure||Understanding Your Shipment||PDF, 3726.3 KB|
|White Paper||Product Stability Study||PDF, 446.0 KB|
|Spreadsheet||Pathogen Assay Information||XLSX, 4231.7 KB|
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