GlycoErase™ PHKA1 Knockout HEK293T Cell Line (CAT#: GLJF-0825-JF551)

Description	GlycoErase™ PHKA1 knockout HEK293T cell line lacks PHKA1 expression. PHKA1 encodes the skeletal muscle isoform of the phosphorylase kinase alpha subunit, a critical regulator of glycogen breakdown. Mutations cause glycogen storage disease type IXD. This HEK293T knockout enables studies on glycogenolysis, calcium regulation, and inherited glycogen disorders.
Product Type	KO Cell Lines
Species	Human
Cell Morphology	Epithelial-like, adherent
Passage Ratio	1:2~1:4
Cell Line	HEK293T
Lineage	Embryonic kidney

Cell Viability	>90%
Sterility Test	The sterility test indicated an absence of microbial growth.
Identity Test	STR identification
Mycoplasma Test	Negative
Virus Test	Negative for HIV, HBV and HCV.
Genetic Stability Testing	We conduct cell genetic stability studies in full compliance with ICH guidelines. Our expertise enables us to design and execute a comprehensive testing program tailored to your specific needs and regulatory requirements.
Validation	PCR, Sanger Sequencing
Culture Medium	DMEM & FBS & Penicillin/Streptomycin
Application	Functional assay
Size	1 M cells/vial*2
Product Format	Frozen
Shipping	Dry ice
Availability Status	Made to order
Handling Notes	Upon receipt, this product must be immediately transferred from dry ice to liquid nitrogen (-150°C to -190°C) and stored in a liquid nitrogen tank. Cell viability is critically dependent on proper handling. We cannot guarantee viability if these instructions are not strictly adhered to.
Product Disclaimer	This product is provided for research only, not suitable for human or animal use. Due to the inherent limitations of infectious agent testing, investigators must exercise extreme caution when handling cells provided by Creative Biolabs, treating all cells as potentially biohazardous.

Target	PHKA1
Full Name	Phosphorylase Kinase Regulatory Subunit Alpha 1
Alternative Name	PHKA
Location	Xq13.1
Gene ID	5255
Summary	Phosphorylase kinase is a complex enzyme with subunits alpha, beta, gamma, and delta. The alpha subunit, encoded by this gene, is involved in muscle glycogen storage disease type 9D. Alternative splicing results in multiple isoforms.