CEPT1 Human shRNA Plasmid Kit (Locus ID 10390)

SKU
TR313975
CEPT1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector, 5µg of each construct provided
  $883.00
2 Weeks*
Specifications
Specifications
Product Data
Locus ID 10390
Vector pRS
E. coli Selection Ampicillin
Mammalian Cell Selection Puromycin
Format Retroviral plasmids
Components CEPT1 - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 10390). 5µg purified plasmid DNA per construct
29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free.
RefSeq NM_001007794, NM_001330743, NM_006090, NR_138483, NR_138484, NR_138485, NM_001007794.1, NM_001007794.2, NM_006090.1, NM_006090.2, NM_006090.3, NM_006090.4, BC032610, BC032610.2, BC049196, NM_006090.5
UniProt ID Q9Y6K0
Summary This gene codes for a choline/ethanolaminephosphotransferase, which functions in the synthesis of choline- or ethanolamine- containing phospholipids. Alternative splicing results in multiple transcript variants. provided by RefSeq, Aug 2016
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.
Storage Store at -20°C
Shipping Ambient
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Documents
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file-alt Citations

Long-term autophagy is sustained by activation of CCTβ3 on lipid droplets
Ogasawara, Cheng, Tatematsu et al
Nature communications (2020) 11 (1), 4480 DOI: 10.1038/s41467-020-18153-w
Cited by 41
AI Summary: In this study, OriGene’s shRNA products TR313975D (for CEPT1) and TR305398C (for CHPT1) were used to generate stable knockdown cell lines, enabling the investigation of these genes' roles in autophagy regulation.
Snippet: (synthesized by Japan Bio Service). The siRNAs were transfected using Lipofectamine RNAiMAX (Thermo Fisher). For human CEPT1 and CHPT1, stable cell lines harboring shRNAs (TR313975D and TR305398C, Origene) were generated as described below using retroviral vectors. Retroviral production and generation of stable cell lines by infection PLAT-E cells63 and pMXs-IRES-Puro vector64 were kindly prov
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Showing 1-1 of 1 papers.
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