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Found 1 matching solution for this experiment
pGS-CD62L
Peter D. Sun, Structural Immunology Section, Laboratory of Immun
Upstream tips |
Protocol tips |
Downstream tips |
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CHO-lec3.2.8.1 cells were grown in a 100 cm2 flask until approximately 80% confluence and transfected with a mixture of 30 μg sterile-filtered pGS-CD62L plasmid DNA, 90 μL Lipofactamine 3000, 60 μL P3000 reagent, and 3 mL Opti-MEM. After 20 hours of incubation at 37 °C, cells were trypsinized, resuspended in 200 mL selection medium containing 30 μM MSX, diluted seven-fold, and plated into ten 384 well plates with 50 μL per well. |
Selective medium replacements were made for wells exhibiting color change and the CD62L expressions were measured by ELISA following a manufacture’s instruction (R&D systems, Inc). The top 10% CD62L expression clones were trypsinized and transferred to 48 well plates, and their expressions were evaluated again by ELISA upon confluence. |
Protocol tips |
CHO-lec3.2.8.1 cells were grown in a 100 cm2 flask until approximately 80% confluence and transfected with a mixture of 30 μg sterile-filtered pGS-CD62L plasmid DNA, 90 μL Lipofactamine 3000, 60 μL P3000 reagent, and 3 mL Opti-MEM. After 20 hours of incubation at 37 °C, cells were trypsinized, resuspended in 200 mL selection medium containing 30 μM MSX, diluted seven-fold, and plated into ten 384 well plates with 50 μL per well. |
Downstream tips |
Selective medium replacements were made for wells exhibiting color change and the CD62L expressions were measured by ELISA following a manufacture’s instruction (R&D systems, Inc). The top 10% CD62L expression clones were trypsinized and transferred to 48 well plates, and their expressions were evaluated again by ELISA upon confluence. |
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