TPCN2 Knockout cell line (T98G)

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TPCN2 Knockout cell line (T98G)

TPCN2 Knockout cell line (T98G) Order

Catalog#YKO-H793

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-H793
Cell line TPCN2 Knockout cell line (T98G) Cell Type T98G Cell Line
Morphology Fibroblast,adherent Passage ratio 1:2-1:4
Culture method 88%MEM+10%FBS+1%NEAA+1%Sodium Pyruvate 100 mM Solution
Cryopreservation solution 90%FBS+10%DMSO
Special Note

Gene Information

Official symbol
TPCN2
Gene id
219931
Official full symbol
two pore segment channel 2
Also known as
SHEP10, TPC2
This gene encodes a putative cation-selective ion channel with two repeats of a six-transmembrane-domain. The protein localizes to lysosomal membranes and enables nicotinic acid adenine dinucleotide phosphate (NAADP) -induced calcium ion release from lysosome-related stores. This ubiquitously expressed gene has elevated expression in liver and kidney. Two common nonsynonymous SNPs in this gene strongly associate with blond versus brown hair pigmentation.

KO strategy

Knockout region: None (based on transcript TPCN2-201)
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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