Hereditary Hemochromatosis Protein (HFE) Protein
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Description
HFE is a recombinant protein.
Documents del producto
Product specifications
| Category | Proteins and Peptides |
| Immunogen Target | HFE |
| Conjugation | Unconjugated |
| Expression | Recombinant |
| Purity | > 85% (SDS-PAGE) |
| Size 1 | 5 µg |
| Size 2 | 20 µg |
| Size 3 | 1 mg |
| Form | Liquid |
| Tested Applications | SDS-PAGE |
| Availability | Shipped within 5-10 working days. |
| Dry Ice | No |
| UniProt ID | Q30201 |
| Background | Protein HFE |
| Status | RUO |
| Note | This product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use. |
Descripción
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HFE antibody
Binds to transferrin receptor(TFR) and reduces its affinity for iron-loaded transferrin.
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Hereditary Hemochromatosis Protein (HFE) Antibody
HFE Antibody is a Rabbit Polyclonal antibody against 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 (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].
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Hereditary Hemochromatosis Protein (HFE) Antibody
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.
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