lipofectin method (Thermo Fisher)
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lipofectin method
Lipofectin Method, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/lipofectin+method/pm23921576-61-39-41
Average 86 stars, based on 1 article reviews
Lipofectin Method, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/lipofectin+method/pm23921576-61-39-41
Average 86 stars, based on 1 article reviews
lipofectin method - by Bioz Stars,
2026-10
86/100 stars
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Transfection:Article Title: Conditional expression of PTEN alters the androgen responsiveness of prostate cancer cells. Article Snippet: Z. Wu, M. Conaway, D. Gioeli, M.J. Weber, and D. Theodorescu* DepartmentofMolecular PhysiologyandBiological Physics,Universityof VirginiaHealth Sciences Center, Charlottesville,Virginia DepartmentofHealth Evaluation Sciences (Biostatistics),Universityof VirginiaHealth SciencesCenter, Charlottesville,Virginia DepartmentofMicrobiology,Universityof VirginiaHealth Sciences Center,Charlottesville,Virginia Article Title: Method for regulating genes with electromagnetic response elements Article Snippet: .. Materials and Methods Cell Culture and Transfections As previously described, HeLa cells were used for transient transfections and the Article Title: Differential Ras activation between caveolae/raft and non-raft microdomains. Article Snippet: .. Cell culture, transfection, and imaging COS cells were transfected with pRaichu-tH or pRaichu-tK using the Article Title: Bromodomain analysis of Brd2-dependent transcriptional activation of cyclin A Article Snippet: .. Low passage NIH/3T3 cells (A.T.C.C., Manassas, VA, U.S.A.) were grown in DMEM (Dulbecco's modified Eagle's medium; Invitrogen) supplemented with 10% normal calf serum and PSG (penicillin, streptomycin and glutamine), maintained at less than 75% confluence and transfected in triplicate in 60 mm dishes at 50% confluence with plasmids by the Article Title: A novel double-enhanced suicide gene therapy in a colon cancer cell line mediated by gef and apoptin. Article Snippet: Background Double-suicide gene therapy is a promising strategy for the treatment of advanced cancer.. It has become an important research line in the development of gene therapy to overcome the drawbacks of single-gene therapy.. Objective The aim of this study was to investigate the usefulness of double-suicide gene therapy with the two suicide genes, gef and apoptin, in colon carcinoma. Article Title: A novel point mutation in the ligand-binding domain (LBD) of the human glucocorticoid receptor (hGR) causing generalized glucocorticoid resistance: the importance of the C terminus of hGR LBD in conferring transactivational activity. Article Snippet: .. CV-1, COS-7, and HCT-116 cells were transfected using the other:Article Title: Novel codon-optimized GM-CSF gene as an adjuvant to enhance the immunity of a DNA vaccine against HIV-1 Gag. Article Snippet: NIH3T3, CT-26, and eLa cells were transfected by the Cell Culture:Article Title: Method for regulating genes with electromagnetic response elements Article Snippet: .. Materials and Methods Cell Culture and Transfections As previously described, HeLa cells were used for transient transfections and the Article Title: Differential Ras activation between caveolae/raft and non-raft microdomains. Article Snippet: .. Cell culture, transfection, and imaging COS cells were transfected with pRaichu-tH or pRaichu-tK using the Imaging:Article Title: Differential Ras activation between caveolae/raft and non-raft microdomains. Article Snippet: .. Cell culture, transfection, and imaging COS cells were transfected with pRaichu-tH or pRaichu-tK using the Modification:Article Title: Bromodomain analysis of Brd2-dependent transcriptional activation of cyclin A Article Snippet: .. Low passage NIH/3T3 cells (A.T.C.C., Manassas, VA, U.S.A.) were grown in DMEM (Dulbecco's modified Eagle's medium; Invitrogen) supplemented with 10% normal calf serum and PSG (penicillin, streptomycin and glutamine), maintained at less than 75% confluence and transfected in triplicate in 60 mm dishes at 50% confluence with plasmids by the Construct:Article Title: Bromodomain analysis of Brd2-dependent transcriptional activation of cyclin A Article Snippet: .. Low passage NIH/3T3 cells (A.T.C.C., Manassas, VA, U.S.A.) were grown in DMEM (Dulbecco's modified Eagle's medium; Invitrogen) supplemented with 10% normal calf serum and PSG (penicillin, streptomycin and glutamine), maintained at less than 75% confluence and transfected in triplicate in 60 mm dishes at 50% confluence with plasmids by the Article Title: Tat-dependent repression of human immunodeficiency virus type 1 long terminal repeat promoter activity by fusion of cellular transcription factors. Article Snippet: Transcription initiation from HIV-1 long terminal repeat (LTR) promoter requires the virally encoded transactivator, Tat, and several cellular co-factors to accomplish the Tat-dependent processive transcription elongation.. Individual cellular transcription activators, LBP-1b and Oct-1, on the other hand, have been shown to inhibit LTR promoter activities probably via competitive binding against TFIID to the TATA-box in LTR promoter.. To explore the genetic interference strategies against the viral replication, we took advantage of the existence of the bipartite DNA binding domains and the repression domains of LBP-1b and Oct-1 factors to generate a chimeric transcription repressor. Luciferase:Article Title: Bromodomain analysis of Brd2-dependent transcriptional activation of cyclin A Article Snippet: .. Low passage NIH/3T3 cells (A.T.C.C., Manassas, VA, U.S.A.) were grown in DMEM (Dulbecco's modified Eagle's medium; Invitrogen) supplemented with 10% normal calf serum and PSG (penicillin, streptomycin and glutamine), maintained at less than 75% confluence and transfected in triplicate in 60 mm dishes at 50% confluence with plasmids by the Expressing:Article Title: Bromodomain analysis of Brd2-dependent transcriptional activation of cyclin A Article Snippet: .. Low passage NIH/3T3 cells (A.T.C.C., Manassas, VA, U.S.A.) were grown in DMEM (Dulbecco's modified Eagle's medium; Invitrogen) supplemented with 10% normal calf serum and PSG (penicillin, streptomycin and glutamine), maintained at less than 75% confluence and transfected in triplicate in 60 mm dishes at 50% confluence with plasmids by the Article Title: Tat-dependent repression of human immunodeficiency virus type 1 long terminal repeat promoter activity by fusion of cellular transcription factors. Article Snippet: Transcription initiation from HIV-1 long terminal repeat (LTR) promoter requires the virally encoded transactivator, Tat, and several cellular co-factors to accomplish the Tat-dependent processive transcription elongation.. Individual cellular transcription activators, LBP-1b and Oct-1, on the other hand, have been shown to inhibit LTR promoter activities probably via competitive binding against TFIID to the TATA-box in LTR promoter.. To explore the genetic interference strategies against the viral replication, we took advantage of the existence of the bipartite DNA binding domains and the repression domains of LBP-1b and Oct-1 factors to generate a chimeric transcription repressor. Incubation:Article Title: A novel double-enhanced suicide gene therapy in a colon cancer cell line mediated by gef and apoptin. Article Snippet: Background Double-suicide gene therapy is a promising strategy for the treatment of advanced cancer.. It has become an important research line in the development of gene therapy to overcome the drawbacks of single-gene therapy.. Objective The aim of this study was to investigate the usefulness of double-suicide gene therapy with the two suicide genes, gef and apoptin, in colon carcinoma. Selection:Article Title: A novel double-enhanced suicide gene therapy in a colon cancer cell line mediated by gef and apoptin. Article Snippet: Background Double-suicide gene therapy is a promising strategy for the treatment of advanced cancer.. It has become an important research line in the development of gene therapy to overcome the drawbacks of single-gene therapy.. Objective The aim of this study was to investigate the usefulness of double-suicide gene therapy with the two suicide genes, gef and apoptin, in colon carcinoma. |