TMEM214 Knockout cell line (ARPE-19)

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TMEM214 Knockout cell line (ARPE-19)

TMEM214 Knockout cell line (ARPE-19) Order

Catalog#YKO-H616

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-H616
Cell line TMEM214 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
TMEM214
Gene id
54867
Official full symbol
transmembrane protein 214
Also known as
None
None

KO strategy

Knockout region: Exon 2 (based on transcript TMEM214-201)
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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