GlycoErase™ TPI1 Knockout HepG2 Cell Line (CAT#: GLJF-0825-JF718)

Description	GlycoErase™ TPI1 knockout HepG2 cell line removes TPI1, encoding triosephosphate isomerase, a key enzyme in glycolysis and gluconeogenesis. This knockout facilitates studies on glycolytic flux control, redox and energy balance, and enzymopathy, with applications in metabolic research and rare disease modeling, especially in liver cells.
Product Type	KO Cell Lines
Species	Human
Cell Morphology	Epithelial-like, adherent
Passage Ratio	1:4~1:6
Cell Line	HepG2
Primary Disease	Hepatoblastoma
Lineage	Liver
Lineage Subtype	Hepatoblastoma

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 & Glutamine
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	TPI1
Full Name	Triosephosphate Isomerase 1
Alternative Name	TIM; TPI; TPID; HEL-S-49
Location	12p13.31
Gene ID	7167
Summary	The enzyme encoded here catalyzes the G3P and DHAP interconversion in glycolysis and gluconeogenesis. Defects cause triosephosphate isomerase deficiency. Pseudogenes exist on four chromosomes, and alternative splicing produces variant isoforms.