Human PSEN1 knockout PC-3 cell line

Description

Recommended control: Human wild-type PC-3 cell line ab290718 . Please note a wild-type cell line is not automatically included with a knockout cell line order, if required please add recommended wild-type cell line at no additional cost using the code WILDTYPE-TMTK1. Cryopreservation cell medium: Cell Freezing Medium-DMSO Serum free media, contains 8.7 % DMSO in MEM supplemented with methyl cellulose. Culture medium: F-12K + 10 % FBS Initial handling guidelines: Upon arrival, the vial should be stored in liquid nitrogen vapor phase and not at -80C. Storage at -80C may result in loss of viability. 1. Thaw the vial in 37C water bath for approximately 1-2 minutes. 2. Transfer the cell suspension 0.8 mL to a 15 mL/50 mL conical sterile polypropylene centrifuge tube containing 8.4 mL pre-warmed culture medium, wash vial with an additional 0.8 mL culture medium total volume 10 mL to collect remaining cells, and centrifuge at 201 x g rcf for 5 minutes at room temperature. 10 mL represents minimum recommended dilution. 20 mL represents maximum recommended dilution. 3. Resuspend the cell pellet in 5 mL pre-warmed culture medium and count using a haemocytometer or alternative cell counting method. Based on cell count, seed cells in an appropriate cell culture flask at a density of 2x104 cells/cm2. Seeding density is given as a guide only and should be scaled to align with individual lab schedules. 4. Incubate the culture at 37C incubator with 5 % CO2. Cultures should be monitored daily. Subculture guidelines: All seeding densities should be based on cell counts gained by established methods. A guide seeding density of 2x104 cells/cm2 is recommended. A partial media change 24 hours prior to subculture may be helpful to encourage growth, if required. Cells should be passaged when they have achieved 80-90 % confluence. We will provide viable cells that proliferate on revival. This product is subject to limited use licenses from The Broad Institute and ERS Genomics Limited, and is developed with patented technology. For full details of the limited use licenses and relevant patents please refer to our limited use license and patent pages.