jetprime dna/sirna (Sartorius AG)
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jetprime dna/sirna
Jetprime Dna/Sirna, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 11113 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/jetprime/jetPRIME+DNA%2FsiRNA/custom%40101000027%4042639794
Average 99 stars, based on 11113 article reviews
Jetprime Dna/Sirna, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 11113 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/jetprime/jetPRIME+DNA%2FsiRNA/custom%40101000027%4042639794
Average 99 stars, based on 11113 article reviews
jetprime dna/sirna - by Bioz Stars,
2026-09
99/100 stars
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Cell Culture:Article Title: Method for producing t cells modified by chimeric antigen receptor Article Snippet: .. Specific steps are as follows. (1) The 293FT cell culture flask (T175) that had reached 80%-90% was taken out from the cell incubator in 5% CO2 at 37° C., the cells were collected and washed after digestion, 4.5×106 cells and 9 mL of DMEM complete medium (purchased from Gibco, product catalog No.: 11965-084) were added to each 10 cm-cell culture dish and gently shaken, and the resulting mixture was put in the incubator in 5% CO2 at 37° C. (2) On the second day of culturing, the following reagents were added to each culture dish: 500 μL of Recombinant:Article Title: Method for producing t cells modified by chimeric antigen receptor Article Snippet: .. Specific steps are as follows. (1) The 293FT cell culture flask (T175) that had reached 80%-90% was taken out from the cell incubator in 5% CO2 at 37° C., the cells were collected and washed after digestion, 4.5×106 cells and 9 mL of DMEM complete medium (purchased from Gibco, product catalog No.: 11965-084) were added to each 10 cm-cell culture dish and gently shaken, and the resulting mixture was put in the incubator in 5% CO2 at 37° C. (2) On the second day of culturing, the following reagents were added to each culture dish: 500 μL of Plasmid Preparation:Article Title: Method for producing t cells modified by chimeric antigen receptor Article Snippet: .. Specific steps are as follows. (1) The 293FT cell culture flask (T175) that had reached 80%-90% was taken out from the cell incubator in 5% CO2 at 37° C., the cells were collected and washed after digestion, 4.5×106 cells and 9 mL of DMEM complete medium (purchased from Gibco, product catalog No.: 11965-084) were added to each 10 cm-cell culture dish and gently shaken, and the resulting mixture was put in the incubator in 5% CO2 at 37° C. (2) On the second day of culturing, the following reagents were added to each culture dish: 500 μL of Article Title: A novel adenovirus 19K/IX protein promotes infection by preventing proteasomal degradation of tyrosine-ubiquitinated capsid protein pIX Article Snippet: Plasmid encoding HA-Ubiquitin was purchased from Addgene (#17608), the His-Ubiquitin expressing plasmid has been described before [ ]. .. All plasmid transfections were performed with the Article Title: Targeting UBE2T by β-elemene inhibits prostate cancer stem cells and bone metastasis by blocking the TRIM28/pGSK3β/β-catenin signaling. Article Snippet: .. Briefly, Plasmid transfection was performed using Transfection:Article Title: A novel adenovirus 19K/IX protein promotes infection by preventing proteasomal degradation of tyrosine-ubiquitinated capsid protein pIX Article Snippet: Plasmid encoding HA-Ubiquitin was purchased from Addgene (#17608), the His-Ubiquitin expressing plasmid has been described before [ ]. .. All plasmid transfections were performed with the Article Title: FOXC2 represses NFAT1-dependent transcription through a DNA-facilitated protein–protein interaction Article Snippet: .. The cells were transfected with pcDNA3.1–NFAT1 and pcDNA3.1–FOXC2 plasmids for 48 h using Article Title: Targeting UBE2T by β-elemene inhibits prostate cancer stem cells and bone metastasis by blocking the TRIM28/pGSK3β/β-catenin signaling. Article Snippet: .. Briefly, Plasmid transfection was performed using Article Title: The proximal N-terminus of IRAG is required for potentiation of HCN4 channels Article Snippet: .. Transient transfection of HCN4 constructs and/or IRAG was performed using Fugene6 (Promega, Madison, WI) or Article Title: SNHG7 interacts with PCBP2 to promote CDKN2A expression and modulate cuproptosis in colorectal cancer Article Snippet: .. They were transfected into SW480 and RKO cells according to the manufacturer's instructions by Article Title: DNA-PK interacts with cyclic dinucleotides and inhibits type I interferon responses Article Snippet: Flow cytometry data were then analyzed using the NovoExpress software (Agilent), while fluorescence microscopy data were analyzed with Harmony software (Revvity). .. T98G cells grown on coverslips were transfected with 1 μg/ml 2′3′-cGAMP–iFluor 488 (#20320; AAT BioQuest) or DMSO (control) using Article Title: FOXC2 represses NFAT1-dependent transcription through a DNA-facilitated protein-protein interaction. Article Snippet: .. The cells were transfected with pcDNA3.1 –NFAT1 and pcDNA3.1 –FOXC2 plasmids for 48 h using Knockdown:Article Title: Targeting UBE2T by β-elemene inhibits prostate cancer stem cells and bone metastasis by blocking the TRIM28/pGSK3β/β-catenin signaling. Article Snippet: .. Briefly, Plasmid transfection was performed using Expressing:Article Title: Targeting UBE2T by β-elemene inhibits prostate cancer stem cells and bone metastasis by blocking the TRIM28/pGSK3β/β-catenin signaling. Article Snippet: .. Briefly, Plasmid transfection was performed using Construct:Article Title: The proximal N-terminus of IRAG is required for potentiation of HCN4 channels Article Snippet: .. Transient transfection of HCN4 constructs and/or IRAG was performed using Fugene6 (Promega, Madison, WI) or Control:Article Title: DNA-PK interacts with cyclic dinucleotides and inhibits type I interferon responses Article Snippet: Flow cytometry data were then analyzed using the NovoExpress software (Agilent), while fluorescence microscopy data were analyzed with Harmony software (Revvity). .. T98G cells grown on coverslips were transfected with 1 μg/ml 2′3′-cGAMP–iFluor 488 (#20320; AAT BioQuest) or DMSO (control) using |