GRLF1 (ARHGAP35) Human shRNA Plasmid Kit (Locus ID 2909)
CAT#: TL312603
ARHGAP35 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector, 5µg of each construct provided
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CNY 5,740.00
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CNY 4,070.00
Specifications
Product Data | |
Product Name | GRLF1 (ARHGAP35) Human shRNA Plasmid Kit (Locus ID 2909) |
Locus ID | 2909 |
UniProt ID | Q9NRY4 |
Synonyms | GRF-1; GRLF1; P190-A; P190A; p190ARhoGAP; p190RhoGAP |
Vector | pGFP-C-shLenti |
Format | Lentiviral plasmids |
Kit Components | ARHGAP35 - Human, 4 unique 29mer shRNA constructs in lentiviral GFP vector(Gene ID = 2909). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pGFP-C-shLenti Vector, TR30021, included for free. |
RefSeq | NM_004491, NM_024342, NM_004491.1, NM_004491.2, NM_004491.3, NM_004491.4, BC003514, BC065491, BC131565, BC150257, BM855708 |
Summary | The human glucocorticoid receptor DNA binding factor, which associates with the promoter region of the glucocorticoid receptor gene (hGR gene), is a repressor of glucocorticoid receptor transcription. The amino acid sequence deduced from the cDNA sequences show the presence of three sequence motifs characteristic of a zinc finger and one motif suggestive of a leucine zipper in which 1 cysteine is found instead of all leucines. The GRLF1 enhances the homologous down-regulation of wild-type hGR gene expression. Biochemical analysis suggests that GRLF1 interaction is sequence specific and that transcriptional efficacy of GRLF1 is regulated through its interaction with specific sequence motif. The level of expression is regulated by glucocorticoids. [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. |
Performance Guaranteed | OriGene guarantees that the sequences in the shRNA expression cassettes are verified to correspond to the target gene with 100% identity. One of the four constructs at minimum are guaranteed to produce 70% or more gene expression knock-down provided a minimum transfection efficiency of 80% is achieved. Western Blot data is recommended over qPCR to evaluate the silencing effect of the shRNA constructs 72 hrs post transfection. To properly assess knockdown, the gene expression level from the included scramble control vector must be used in comparison with the target-specific shRNA transfected samples. For non-conforming shRNA, requests for replacement product must be made within ninety (90) days from the date of delivery of the shRNA kit. To arrange for a free replacement with newly designed constructs, please contact Technical Services at techsupport@origene.com. Please provide your data indicating the transfection efficiency and measurement of gene expression knockdown compared to the scrambled shRNA control (Western Blot data preferred). |
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