CCDC86 Knockout cell line(NCI-H1299)

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CCDC86 Knockout cell line(NCI-H1299)

CCDC86 Knockout cell line(NCI-H1299) Order

Catalog#YKO-H516

Price (USD)-

Size 1*10^6

Instruction

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.

Cell Info

Catalog YKO-H516
Cell line CCDC86 Knockout cell line(NCI-H1299) Cell Type Human Non-small Cell Lung Carcinoma Cell Line
Morphology Epithelial-like, adherent Passage ratio 1:3~1:6
Culture method 88%RPMI-1640+10% FBS+1%Glutamax+1%Sodium Pyruvate
Cryopreservation solution 90%FBS+10%DMSO
Special Note

STR Validation

Gene Information

Official symbol
CCDC86
Gene id
79080
Official full symbol
coiled-coil domain containing 86
Also known as
None
Enables RNA binding activity. Located in chromosome; nucleolus; and nucleoplasm.

KO strategy

Knockout region: Exon 1 (based on transcript CCDC86-201)
Validation: PCR+Sanger Sequencing

Method

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.

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