PKC alpha (PRKCA) Human shRNA Lentiviral Particle (Locus ID 5578)
SKU
TL320466V
PRKCA - Human shRNA lentiviral particles (4 unique 29mer target-specific shRNA, 1 scramble control), 0.5 ml each, >10^7 TU/ml.
$1,731.00
5 Weeks*
Specifications
| Product Data | |
| Locus ID | 5578 |
|---|---|
| Synonyms | AAG6; PKC-alpha; PKCA; PKCalpha; PKCI+/-; PRKACA |
| Vector | pGFP-C-shLenti |
| E. coli Selection | Chloramphenicol (34 ug/ml) |
| Mammalian Cell Selection | Puromycin |
| Format | Lentiviral particles |
| Components | PRKCA - Human shRNA lentiviral particles (4 unique 29mer target-specific shRNA, 1 scramble control), 0.5 ml each, >10^7 TU/ml. |
| RefSeq | BC011942, NM_002737, NM_002737.1, NM_002737.2, BC015855, BC053321, BC062759, BC071767, BC103691, BC107592, BC109273, BC109274, BC122530, BM015483 |
| UniProt ID | P17252 |
| Summary | Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. This kinase has been reported to play roles in many different cellular processes, such as cell adhesion, cell transformation, cell cycle checkpoint, and cell volume control. Knockout studies in mice suggest that this kinase may be a fundamental regulator of cardiac contractility and Ca(2+) handling in myocytes. 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). |
| Storage | Store at -80°C |
| Shipping | Dry Ice |
Reviews
Documents
Resources
Citations
Reactivation of fetal splicing programs in diabetic hearts is mediated by protein kinase C signaling
Verma, Deshmukh, Liu et al
J Biol Chem (2013) 288 (49), 35372-86 DOI: 10.1074/jbc.M113.507426
Verma, Deshmukh, Liu et al
J Biol Chem (2013) 288 (49), 35372-86 DOI: 10.1074/jbc.M113.507426
AI Summary: OriGene products, specifically the CELF1 Myc-DDK tagged cDNA (RC201307) and Rbfox2 Myc-DDK tagged cDNA (RC208408) plasmids, were used in this study to overexpress and analyze the roles of CELF1 and Rbfox2 proteins in mediating PKC-dependent alternative splicing changes in diabetic hearts.
Showing 1-1 of 1 papers.
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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen
complexities in the preparation of your product. International customers may expect an additional 1-2 weeks
in shipping.
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