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HFE (NM_139003) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC219194L4V
- LentiORF®
-
Lenti ORF particles, HFE (mGFP-tagged)-Human hemochromatosis (HFE), transcript variant 3, 200ul, >10^7 TU/mL
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CNY 8,360.00
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Specifications
| Product Data | |
| Product Name | HFE (NM_139003) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | HFE1; HH; HLA-H; MVCD7; TFQTL2 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_139003 |
| ORF Size | 726 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC219194).
|
| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_139003.2 |
| RefSeq Size | 1904 bp |
| RefSeq ORF | 729 bp |
| Locus ID | 3077 |
| Protein Families | Druggable Genome, Transmembrane |
| MW | 27.7 kDa |
| Gene 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] |
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