prd shgfp non effective (OriGene)
94
Structured Review
OriGene
prd shgfp non effective
Prd Shgfp Non Effective, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 73 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/prd+shgfp+non+effective/Negative+shRNA+control+in+pRS+Vector/pm21841822-225-37-39
Average 94 stars, based on 73 article reviews
Prd Shgfp Non Effective, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 73 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/prd+shgfp+non+effective/Negative+shRNA+control+in+pRS+Vector/pm21841822-225-37-39
Average 94 stars, based on 73 article reviews
prd shgfp non effective - by Bioz Stars,
2026-10
94/100 stars
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Knockdown:Article Title: Deacetylation of FOXO3 by SIRT1 or SIRT2 leads to Skp2-mediated FOXO3 ubiquitination and degradation. Article Snippet: Skp2-targeting shRNA (50-TCTAAGCCTGGAAGG CCTG-30) and GFP shRNA (50-GCAAGCTGACCCTGAA GTTC-30) were subcloned into the pSUPER-puro vector (Oligoengine, Seattle, WA, USA), followed by transfection into Phoenix packaging cells and infection into DU145 cells according to the standard procedure (Brummelkamp et al., 2002). .. These plasmids also were used for transient knockdown of Skp2 in HEK293T cells by transient transfection. pRSshSIRT1 plasmid (Origene, Rockville, MD, USA, TI337728, 50-TTATTTGGCTACACTAAAGAATGCAGTAT-30) was used for transient knockdown of SIRT1 in HEK293T cells and DU145 cells. Transfection:Article Title: Deacetylation of FOXO3 by SIRT1 or SIRT2 leads to Skp2-mediated FOXO3 ubiquitination and degradation. Article Snippet: Skp2-targeting shRNA (50-TCTAAGCCTGGAAGG CCTG-30) and GFP shRNA (50-GCAAGCTGACCCTGAA GTTC-30) were subcloned into the pSUPER-puro vector (Oligoengine, Seattle, WA, USA), followed by transfection into Phoenix packaging cells and infection into DU145 cells according to the standard procedure (Brummelkamp et al., 2002). .. These plasmids also were used for transient knockdown of Skp2 in HEK293T cells by transient transfection. pRSshSIRT1 plasmid (Origene, Rockville, MD, USA, TI337728, 50-TTATTTGGCTACACTAAAGAATGCAGTAT-30) was used for transient knockdown of SIRT1 in HEK293T cells and DU145 cells. Plasmid Preparation:Article Title: Deacetylation of FOXO3 by SIRT1 or SIRT2 leads to Skp2-mediated FOXO3 ubiquitination and degradation. Article Snippet: Skp2-targeting shRNA (50-TCTAAGCCTGGAAGG CCTG-30) and GFP shRNA (50-GCAAGCTGACCCTGAA GTTC-30) were subcloned into the pSUPER-puro vector (Oligoengine, Seattle, WA, USA), followed by transfection into Phoenix packaging cells and infection into DU145 cells according to the standard procedure (Brummelkamp et al., 2002). .. These plasmids also were used for transient knockdown of Skp2 in HEK293T cells by transient transfection. pRSshSIRT1 plasmid (Origene, Rockville, MD, USA, TI337728, 50-TTATTTGGCTACACTAAAGAATGCAGTAT-30) was used for transient knockdown of SIRT1 in HEK293T cells and DU145 cells. Control:Article Title: Deacetylation of FOXO3 by SIRT1 or SIRT2 leads to Skp2-mediated FOXO3 ubiquitination and degradation. Article Snippet: Skp2-targeting shRNA (50-TCTAAGCCTGGAAGG CCTG-30) and GFP shRNA (50-GCAAGCTGACCCTGAA GTTC-30) were subcloned into the pSUPER-puro vector (Oligoengine, Seattle, WA, USA), followed by transfection into Phoenix packaging cells and infection into DU145 cells according to the standard procedure (Brummelkamp et al., 2002). .. These plasmids also were used for transient knockdown of Skp2 in HEK293T cells by transient transfection. pRSshSIRT1 plasmid (Origene, Rockville, MD, USA, TI337728, 50-TTATTTGGCTACACTAAAGAATGCAGTAT-30) was used for transient knockdown of SIRT1 in HEK293T cells and DU145 cells. |