M6PR Knockout Cell Line - CD BioSciences

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M6PR Knockout Cell Line

M6PR Knockout Cell Line

SPL-01930

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1 Unit Online Inquiry
Description
8bp deletion
Target Information
Target Name M6PR
Gene Abbr. M6PR
Gene ID 4074
Full Name mannose-6-phosphate receptor, cation dependent
Alias CD-M6PR, CD-MPR, MPR 46, MPR-46, MPR46
Species Human
Genomic Locus chr12:8945519
Transcript NM_002355
WT Expression Level 342.16 TPM (TPM = Transcripts per million; any value less than 3 is considered non-expressing)
Introduction This gene encodes a member of the P-type lectin family. P-type lectins play a critical role in lysosome function through the specific transport of mannose-6-phosphate-containing acid hydrolases from the Golgi complex to lysosomes. The encoded protein functions as a homodimer and requires divalent cations for ligand binding. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. A pseudogene of this gene is located on the long arm of chromosome X. [provided by RefSeq, May 2011].
Product Details
Cell Line Model HAP1
Genotype HAP1 cell line, edited by CRISPR/Cas to contain a 8bp deletion in a coding exon of M6PR.
Description 8bp deletion
Parental Cell Line C631
Guide RNA Sequence TTCAGGGTGTGCCGGGAAGC
PCR Primer Forward: GGTAGGAAGGGGAGTTTTCTTACTT
Reverse: CAAATATTCACTCAGCCATGACCTC
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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