Ano6 Mouse shRNA Plasmid (Locus ID 105722)
CAT#: TR511035
Ano6 - Mouse, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
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CNY 4,790.00
货期*
现货
规格
Cited in 1 publication. |
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经常一起买 (1)
Specifications
Product Data | |
Product Name | Ano6 Mouse shRNA Plasmid (Locus ID 105722) |
Locus ID | 105722 |
UniProt ID | Q6P9J9 |
Synonyms | 2900059G15Rik; AA407480; AW554778; F730003B03Rik; Tmem16f |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | Ano6 - Mouse, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 105722). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | BC060732, NM_001253813, NM_175344, NM_175344.1, NM_175344.2, NM_175344.3, NM_175344.4, NM_001253813.1, BC023745, BC052511 |
Summary | Small-conductance calcium-activated nonselective cation (SCAN) channel which acts as a regulator of phospholipid scrambling in platelets, osteoblasts and fetal thymocytes. Phospholipid scrambling results in surface exposure of phosphatidylserine which in platelets is essential to trigger the clotting system whereas in osteoblasts is essential for the deposition of hydroxyapatite during bone mineralization. Has calcium-dependent phospholipid scramblase activity; scrambles phosphatidylserine, phosphatidylcholine and galactosylceramide. Can generate outwardly rectifying chloride channel currents in airway epithelial cells and Jurkat T lymphocytes.[UniProtKB/Swiss-Prot Function] |
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). |
Citations (1)
The use of this RNAi has been cited in the following citations: |
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Calcium-dependent phospholipid scrambling by TMEM16F
,Jun Suzuki, Masato Umeda, Peter J. Sims, Shigekazu Nagata,
Nature 468, 834-838 (24 November 2010) doi:10.1038/nature09583 Letter
[Ano6]
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