Catalog#:YKO-H621
Price (USD):-
Size: 1*10^6
Exclusive Red Cotton system(en.rc-crispr.com)was used to design the sgRNA fragment knockout strategy. Two sgRNAs were constructed into CRISPR-U™ plasmid which will be subsequentially transfected into cells by electroporation/virus method. And the single-cell clones were isolated by the limited dilution method and the Monoclone Genotype Validation Kit (Cat: YK-MV-1000) was used for cell lysis and PCR amplification on the single-cell clones, and then the genotype was verified by Sanger sequencing. Upon passing the final validation, the positive clones were expanded and cryopreserved.
Catalog | YKO-H621 | ||
Cell line | MILR1 Knockout cell line(THP-1) | Cell Type | Human Ovarian Granulosa Cell Line |
Morphology | Monocyte, suspension | Passage ratio | Control the cell density at 2x10^5~4.0x10^5 cells/ml during passaging, and carry out the passage when the cells grow to 8x10^5~1.0x10^6 cells/ml. |
Culture method | 90%RPMI-1640+10%FBS | ||
Cryopreservation solution | 90%FBS+10%DMSO | ||
Special Note | The cell culture density needs to be strictly controlled. The cell viability after thawing is relatively low, it is recommended to use Australia-sourced FBS for thawing or increase the FBS ratio to 20%. When the cells grow normally and can be passaged after 2 passages, the cells can be cultured using the normal culture method. |