RAB2A Knockout Cell Line - CD BioSciences

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RAB2A Knockout Cell Line

RAB2A Knockout Cell Line

SPL-02928

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Description
14bp deletion
Target Information
Target Name RAB2A
Gene Abbr. RAB2A
Gene ID 5862
Full Name RAB2A, member RAS oncogene family
Alias LHX, RAB2
Species Human
Genomic Locus chr8:60572060
Transcript NM_002865
WT Expression Level 124.97 TPM (TPM = Transcripts per million; any value less than 3 is considered non-expressing)
Introduction The protein encoded by this gene belongs to the Rab family, members of which are small molecular weight guanosine triphosphatases (GTPases) that contain highly conserved domains involved in GTP binding and hydrolysis. The Rabs are membrane-bound proteins, involved in vesicular fusion and trafficking. This protein is a resident of pre-Golgi intermediates, and is required for protein transport from the endoplasmic reticulum (ER) to the Golgi complex. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011].
Product Details
Cell Line Model HAP1
Genotype HAP1 cell line, edited by CRISPR/Cas to contain a 14bp deletion in a coding exon of RAB2A.
Description 14bp deletion
Parental Cell Line C631
Guide RNA Sequence GCTCGAATGATAACTATTGA
PCR Primer Forward: ATAGCTAGTGGCAGATTTGGAGATT
Reverse: GTGTCTAACAAACCATAACAGGCAT
Handling Specifications
Revival Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into 10 mL of pre-warmed media in a 10 cm dish.
Culture Medium IMDM + 10% FCS
Growth Properties Cells are adherent cells that are cultured at 37°C in a humidified atmosphere with 5% CO2. Cells should be passaged every 2-3 days, splitting approximately 1:10-1:20.
Freeze Medium IMDM + 20% FCS + 10% DMSO
Biosafety Level BSL-1
Disclaimer This product is classified under IATA regulations as a GMMO (genetically modified micro-organism) and will ship as UN3245. If applicable, ensure facility meets all requirements per local and country regulations.

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