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Amaxa mouse t cell nucleofector medium
Mouse T Cell Nucleofector Medium, supplied by Amaxa, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+t+cell+nucleofector+medium/nucleofector/us10046028-780-7-6
Average 90 stars, based on 1 article reviews
mouse t cell nucleofector medium - by Bioz Stars, 2026-09
90/100 stars

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Cell Culture:

Article Title: Methods and compositions for modulating PD1
Article Snippet: Briefly, 1×10e7 viable cells were resuspended in 100 μA of Amaxa Nucleofector Solution and transfected either with 4 μg of plasmid containing ZFN pair 14546 and 14545, or 4 μg of mut PD1 Fok1 plasmid containing ZFN pair 14546-FokI EL and 14545-Fok I KK, 2.5 μg of Amaxa pmax GFP vector, or a no DNA control, using Amaxa Nucleofector (program X-01). .. Cells were cultured in 2 ml of fully supplemented Amaxa Mouse T Cell Nucleofector Medium at 30° C. after transfection. .. The next day, one ml of Amaxa Mouse T cell Nucleofector Medium was removed and replaced with one ml of complete media supplemented with 10 U/ml IL-2.

Article Title: Methods and compositions for modulating PD1
Article Snippet: Briefly, 1×10e7 viable cells were resuspended in 100 μl of Amaxa Nucleofector Solution and transfected either with 4 μg of plasmid containing ZFN pair 14546 and 14545, or 4 μg of mut PD1 Fok1 plasmid containing ZFN pair 14546-FokI EL and 14545-Fok I KK, 2.5 μg of Amaxa pmax GFP vector, or a no DNA control, using Amaxa Nucleofector (program X-01). .. Cells were cultured in 2 ml of fully supplemented Amaxa Mouse T Cell Nucleofector Medium at 30° C. after transfection. .. The next day, one ml of Amaxa Mouse T cell Nucleofector Medium was removed and replaced with one ml of complete media supplemented with 10 U/ml IL-2.

Article Title: Methods and compositions for modulating PD1
Article Snippet: Briefly, 1×10e7 viable cells were resuspended in 100 μl of Amaxa Nucleofector Solution and transfected either with 4 μg of plasmid containing ZFN pair 14546 and 14545, or 4 μg of mut PD1 Fok1 plasmid containing ZFN pair 14546-FokI EL and 14545-Fok I KK, 2.5 μg of Amaxa pmax GFP vector, or a no DNA control, using Amaxa Nucleofector (program X-01). .. Cells were cultured in 2 ml of fully supplemented Amaxa Mouse T Cell Nucleofector Medium at 30° C. after transfection. .. The next day, one ml of Amaxa Mouse T cell Nucleofector Medium was removed and replaced with one ml of complete media supplemented with 10 U/ml IL-2.

Transfection:

Article Title: Methods and compositions for modulating PD1
Article Snippet: Briefly, 1×10e7 viable cells were resuspended in 100 μA of Amaxa Nucleofector Solution and transfected either with 4 μg of plasmid containing ZFN pair 14546 and 14545, or 4 μg of mut PD1 Fok1 plasmid containing ZFN pair 14546-FokI EL and 14545-Fok I KK, 2.5 μg of Amaxa pmax GFP vector, or a no DNA control, using Amaxa Nucleofector (program X-01). .. Cells were cultured in 2 ml of fully supplemented Amaxa Mouse T Cell Nucleofector Medium at 30° C. after transfection. .. The next day, one ml of Amaxa Mouse T cell Nucleofector Medium was removed and replaced with one ml of complete media supplemented with 10 U/ml IL-2.

Article Title: Methods and compositions for modulating PD1
Article Snippet: Briefly, 1×10e7 viable cells were resuspended in 100 μl of Amaxa Nucleofector Solution and transfected either with 4 μg of plasmid containing ZFN pair 14546 and 14545, or 4 μg of mut PD1 Fok1 plasmid containing ZFN pair 14546-FokI EL and 14545-Fok I KK, 2.5 μg of Amaxa pmax GFP vector, or a no DNA control, using Amaxa Nucleofector (program X-01). .. Cells were cultured in 2 ml of fully supplemented Amaxa Mouse T Cell Nucleofector Medium at 30° C. after transfection. .. The next day, one ml of Amaxa Mouse T cell Nucleofector Medium was removed and replaced with one ml of complete media supplemented with 10 U/ml IL-2.

Article Title: Methods and compositions for modulating PD1
Article Snippet: Briefly, 1×10e7 viable cells were resuspended in 100 μl of Amaxa Nucleofector Solution and transfected either with 4 μg of plasmid containing ZFN pair 14546 and 14545, or 4 μg of mut PD1 Fok1 plasmid containing ZFN pair 14546-FokI EL and 14545-Fok I KK, 2.5 μg of Amaxa pmax GFP vector, or a no DNA control, using Amaxa Nucleofector (program X-01). .. Cells were cultured in 2 ml of fully supplemented Amaxa Mouse T Cell Nucleofector Medium at 30° C. after transfection. .. The next day, one ml of Amaxa Mouse T cell Nucleofector Medium was removed and replaced with one ml of complete media supplemented with 10 U/ml IL-2.

Electroporation:

Article Title: Antagonizing Peroxisome Proliferator-Activated Receptor α Activity Selectively Enhances Th1 Immunity in Male Mice.
Article Snippet: A pmaxGFP expression vector provided with the kit was also transfected at the same time as the siRNAs. .. After electroporation, mouse CD4+ T cells were recovered from the electroporation cuvette and then were allowed to rest overnight in supplemented Mouse T Cell Nucleofector Medium (Amaxa). ..

other:

Article Title: Regulation of T lymphocyte activation by microRNA-21.
Article Snippet: MicroRNAs are small noncoding RNAs that act as posttranscriptional regulators of gene expression.. To identify microRNAs involved in T cell activation, we performed a microRNA array profiling with Jurkat cells.. We found that microRNA-21 (miR-21), which is upregulated in many tumors by targeting a series of tumor suppressor genes to promote tumor growth, was significantly increased in activated Jurkat cells and primary CD4+ T lymphocytes compared with that in quiescent counterparts.



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