ZNF644 Knockout cell line(ARPE-19)

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ZNF644 Knockout cell line(ARPE-19)

ZNF644 Knockout cell line(ARPE-19) Order

Catalog#YKO-H552

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-H552
Cell line ZNF644 Knockout cell line(ARPE-19) Cell Type Human retinal pigment epithelial cell line
Morphology Epithelial-like, adherent Passage ratio 1:3~1:5
Culture method 90% DMEM/F12+10% FBS
Cryopreservation solution 50%DMEM/F12+40%FBS+10%DMSO
Special Note

STR Validation

Gene Information

Official symbol
ZNF644
Gene id
84146
Official full symbol
zinc finger protein 644
Also known as
BM-005, MYP21, NatF, ZEP-2
The protein encoded by this gene is a zinc finger transcription factor that may play a role in eye development. Defects in this gene have been associated with high myopia. Three transcript variants encoding two different isoforms have been found for this gene.

KO strategy

Knockout region: Exon 3 (based on transcript ZNF644-201)
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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