CD9 Knockout cell line (U-87 MG)

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CD9 Knockout cell line (U-87 MG)

CD9 Knockout cell line (U-87 MG) Order

Catalog#YKO-H786

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-H786
Cell line CD9 Knockout cell line (U-87 MG) Cell Type Human Osteosarcoma Cell Line
Morphology Epithelial-like, adherent Passage ratio 1:3~1:5
Culture method 90% MEM+10%FBS
Cryopreservation solution 50%MEM+40%FBS+10%DMSO
Special Note

STR Validation

Gene Information

Official symbol
CD9
Gene id
928
Official full symbol
CD9 molecule
Also known as
BTCC-1, DRAP-27, MIC3, MRP-1, TSPAN-29, TSPAN29
This gene encodes a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Tetraspanins are cell surface glycoproteins with four transmembrane domains that form multimeric complexes with other cell surface proteins. The encoded protein functions in many cellular processes including differentiation, adhesion, and signal transduction, and expression of this gene plays a critical role in the suppression of cancer cell motility and metastasis.

KO strategy

Knockout region: Exon 3 (based on transcript CD9-201)
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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