DVL3 Knockout cell line(OVCAR-3)

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DVL3 Knockout cell line(OVCAR-3)

DVL3 Knockout cell line(OVCAR-3) Order

Catalog#YKO-H500

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-H500
Cell line DVL3 Knockout cell line(OVCAR-3) Cell Type Human ovarian cancer cell line
Morphology Epithelial-like, adherent Passage ratio 1:3~1:5
Culture method 80%RPMI-1640+20% FBS
Cryopreservation solution 50%RPMI-1640+40% FBS+10%DMSO
Special Note 0.01mg/ml bovine insulin

STR Validation

Gene Information

Official symbol
DVL3
Gene id
1857
Official full symbol
dishevelled segment polarity protein 3
Also known as
DRS3
This gene is a member of a multi-gene family which shares strong similarity with the Drosophila dishevelled gene, dsh. The Drosophila dishevelled gene encodes a cytoplasmic phosphoprotein that regulates cell proliferation.

KO strategy

Knockout region: Exon 2 (based on transcript DVL3-201)
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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