GlycoErase™ FUT9 Knockout Human Prostate Cancer Cell 22RV1 (CAT#: GLJF-0525-JF282)

Description	The FUT9 knockout 22RV1 cell line, deficient in fucosyltransferase 9 involved in Lewis X (LeX) antigen synthesis, can be used to study the role of Lewis X antigen in prostate cancer; the absence of FUT9 may affect cell adhesion, migration, and functions related to Lewis X antigen presentation within the prostate tumor microenvironment.
Product Type	KO Cell Lines
Species	Human
Cell Morphology	Epitheloid cells, adherent
Passage Ratio	1:3~1:10
Cell Line	22RV1
Primary Disease	Prostate Adenocarcinoma
Lineage	Prostate

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 & RPMI
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	FUT9
Full Name	Fucosyltransferase 9
Alternative Name	Fuc-TIX
Location	6q16.1
Gene ID	10690
Summary	Golgi-localized fucosyltransferase that catalyzes the final step in Lewis X (LeX) antigen biosynthesis; essential for organ development during embryogenesis.