FABP5 Knockout cell line(MDA-MB-231)

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FABP5 Knockout cell line(MDA-MB-231)

FABP5 Knockout cell line(MDA-MB-231) Order

Catalog#YKO-H509

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-H509
Cell line FABP5 Knockout cell line(MDA-MB-231) Cell Type Human Breast Cancer Cell Line
Morphology Epithelial-like, adherent Passage ratio 1:3~1:4
Culture method 90%L-15+10%FBS
Cryopreservation solution 90%FBS+10%DMSO
Special Note L-15 medium is formulated for growth of cells in CO2 free system. If using CO2 incubator, seal the flask cap tightly to ensure a CO2-free environment

STR Validation

Gene Information

Official symbol
FABP5
Gene id
2171
Official full symbol
fatty acid binding protein 5
Also known as
E-FABP, EFABP, KFABP, PA-FABP, PAFABP
This gene encodes the fatty acid binding protein found in epidermal cells, and was first identified as being upregulated in psoriasis tissue. Fatty acid binding proteins are a family of small, highly conserved, cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands. FABPs may play roles in fatty acid uptake, transport, and metabolism. Polymorphisms in this gene are associated with type 2 diabetes. The human genome contains many pseudogenes similar to this locus.

KO strategy

Knockout region: Exon 2 (based on transcript FABP5-201)
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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