GlycoErase™ PRKAB1 Knockout HEK293T Cell Line (CAT#: GLJF-0825-JF588)

Description	GlycoErase™ PRKAB1 knockout HEK293T cell line eliminates PRKAB1, the β regulatory subunit of AMPK, which shapes holoenzyme assembly, subcellular localization, and allosteric regulation. This knockout provides a platform to study AMPK structural biology, subunit-specific regulation, and metabolic stress responses for therapeutic discovery.
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	PRKAB1
Full Name	Protein Kinase Amp-Activated Non-Catalytic Subunit Beta 1
Alternative Name	AMPK; HAMPKb
Location	12q24.23
Gene ID	5564
Summary	This gene produces a beta regulatory subunit of AMPK, which influences enzyme localization and activation through myristoylation and phosphorylation. It may act as a scaffold for AMPK assembly.