
Ubigene gene knockout cell lines mediated by optimized CRISPR-Cas9 technology provide reliable in vitro models for investigating gene function, signaling pathways, disease mechanisms, and therapeutic targets.
PHKA1 (phosphorylase kinase regulatory subunit alpha 1) encodes the skeletal muscle alpha subunit of phosphorylase kinase, a multisubunit enzyme complex that regulates glycogen breakdown. The alpha subunit has a regulatory role within the complex, whose catalytic gamma subunit phosphorylates glycogen phosphorylase to promote glycogenolysis. PHKA1 therefore contributes to regulation of muscle glycogen metabolism, and defects in this gene cause X-linked muscle glycogen storage disease.
Each knockout cell line is validated by STR authentication, sterility testing (bacteria/fungi), and mycoplasma screening. Genotype is confirmed by two rounds of PCR and Sanger sequencing. Only clones that pass all QC criteria are released, ensuring reliable identity and performance for downstream applications.

Cas9 cell lines in our cell bank can stably express Cas9 protein. Each Cas9 Stable Cell Line is easy to use and enables gene knockout simply by transfecting gRNA, while transfection of gRNA and donor DNA results in gene knock-in or point mutations
These Cas9 stable cell lines have been used to construct the KO cell lines for various genes, gene KO efficiency 5-10 times improved.
Selected cells, low passages, good cell condition, high activity, applicable for all kinds of gene-editing experiments.

Targeted knockout region: EExon 4
Reference Transcript: NM_001172436
Frameshift Mutation Strategy
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use





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