PKC iota (PRKCI) Human shRNA Plasmid Kit (Locus ID 5584)
CAT#: TR320472
PRKCI - Human, 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 3 publications. |
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经常一起买 (2)
Specifications
Product Data | |
Product Name | PKC iota (PRKCI) Human shRNA Plasmid Kit (Locus ID 5584) |
Locus ID | 5584 |
UniProt ID | P41743 |
Synonyms | DXS1179E; nPKC-iota; PKCI |
Vector | pRS |
Format | Retroviral plasmids |
Kit Components | PRKCI - Human, 4 unique 29mer shRNA constructs in retroviral untagged vector(Gene ID = 5584). 5µg purified plasmid DNA per construct29-mer scrambled shRNA cassette in pRS Vector, TR30012, included for free. |
RefSeq | NM_002740, NM_002740.1, NM_002740.2, NM_002740.3, NM_002740.4, NM_002740.5, BC022016, BC042405, BM767350 |
Summary | This gene encodes a member of the protein kinase C (PKC) family of serine/threonine protein kinases. The PKC family comprises at least eight members, which are differentially expressed and are involved in a wide variety of cellular processes. This protein kinase is calcium-independent and phospholipid-dependent. It is not activated by phorbolesters or diacylglycerol. This kinase can be recruited to vesicle tubular clusters (VTCs) by direct interaction with the small GTPase RAB2, where this kinase phosphorylates glyceraldehyde-3-phosphate dehydrogenase (GAPD/GAPDH) and plays a role in microtubule dynamics in the early secretory pathway. This kinase is found to be necessary for BCL-ABL-mediated resistance to drug-induced apoptosis and therefore protects leukemia cells against drug-induced apoptosis. There is a single exon pseudogene mapped on chromosome X. [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). |
Citations (3)
The use of this RNAi has been cited in the following citations: |
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PRKCI negatively regulates autophagy via PIK3CA/AKT-MTOR signaling
,Qu, L;Li, G;Xia, D;Hongdu, B;Xu, C;Lin, X;Chen, Y;,
Biochem. Biophys. Res. Commun.
,PubMed ID 26792725
[PRKCI]
|
PKC iota promotes ovarian tumor progression through deregulation of cyclin E
,null,
Oncogene
,PubMed ID 26279297
[PRKCI]
|
Identification of a Small Molecule with Synthetic Lethality for K-Ras and Protein Kinase C Iota
,Wei Guo, Shuhong Wu, Jinsong Liu, and Bingliang Fang,
Cancer Res. 2008; 68(18): p. 7403-7408
[PRKCI]
|
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