SPOP Knockout cell line(5637)

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SPOP Knockout cell line(5637)

SPOP Knockout cell line(5637) Order

Catalog#YKO-H520

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-H520
Cell line SPOP Knockout cell line(5637) Cell Type Human bladder carcinoma cell line
Morphology Epithelial-like, adherent Passage ratio 1:2-1:3
Culture method 90%RPMI-1640+10%FBS
Cryopreservation solution 50%RPMI-1640+40%FBS+10%DMSO
Special Note

STR Validation

Gene Information

Official symbol
SPOP
Gene id
8405
Official full symbol
speckle type BTB/POZ protein
Also known as
BTBD32, NEDMACE, NEDMIDF, NSDVS1, NSDVS2, TEF2
This gene encodes a protein that may modulate the transcriptional repression activities of death-associated protein 6 (DAXX), which interacts with histone deacetylase, core histones, and other histone-associated proteins. In mouse, the encoded protein binds to the putative leucine zipper domain of macroH2A1.2, a variant H2A histone that is enriched on inactivated X chromosomes. The BTB/POZ domain of this protein has been shown in other proteins to mediate transcriptional repression and to interact with components of histone deacetylase co-repressor complexes. Alternative splicing of this gene results in multiple transcript variants encoding the same protein.

KO strategy

Knockout region: Exon 6 (based on transcript SPOP-206)
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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