HFE Human shRNA Plasmid Kit (Locus ID 3077)

SKU
TG312470
HFE - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector, 5µg of each construct provided
  $883.00
In Stock*
Specifications
Specifications
Product Data
Locus ID 3077
Synonyms HFE1; HH; HLA-H; MVCD7; TFQTL2
Vector pGFP-V-RS
E. coli Selection Kanamycin
Format Retroviral plasmids
Components HFE - Human, 4 unique 29mer shRNA constructs in retroviral GFP vector(Gene ID = 3077). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pGFP-V-RS Vector, TR30013, included for free.
RefSeq NM_000410, NM_001300749, NM_139002, NM_139003, NM_139004, NM_139005, NM_139006, NM_139007, NM_139008, NM_139009, NM_139010, NM_139011, NM_000410.1, NM_000410.2, NM_000410.3, NM_139004.1, NM_139004.2, NM_139007.1, NM_139007.2, NM_139010.1, NM_139010.2, NM_139003.1, NM_139003.2, NM_139006.1, NM_139006.2, NM_139009.1, NM_139009.2, NM_139008.1, NM_139008.2, NM_139011.1, NM_139011.2, NM_001300749.1, NM_139002.1, NM_139005.1, BC074721, BC117201, BC117203, BC143887, NM_139010.3, NM_139003.3, NM_139009.3, NM_139011.3, NM_139004.3, NM_139008.3, NM_139006.3, NM_139007.3, NM_001300749.2, NM_000410.4
UniProt ID Q30201
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
shRNA Design These shRNA constructs were designed against multiple splice variants at this gene locus. To be certain that your variant of interest is targeted, please contact techsupport@origene.com. If you need a special design or shRNA sequence, please utilize our custom shRNA service.
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