GlycoErase™ RXYLT1 Knockout IST-Mes2 Cell Line (CAT#: GLJF-0425-JF973)

Description	The RXYLT1 knockout IST-Mes2 cell line lacks RXYLT1 protein, ribitol xylosyltransferase 1, predicted to have glycosyltransferase function. RXYLT1 knockout in IST-Mes2 cells enables study of glycosyltransferase function disruption in Pleural Mesothelioma, potentially affecting unknown glycosylation pathways and requiring further research to define RXYLT1's role in tumors.
Product Type	KO Cell Lines
Species	Human
Cell Morphology	Epithelial-like, adherent
Passage Ratio	1:2~1:8
Cell Line	IST-Mes2
Primary Disease	Pleural mesothelioma
Lineage	Pleura
Lineage Subtype	Pleural mesothelioma

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	2 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	RXYLT1
Full Name	Ribitol xylosyltransferase 1
Alternative Name	HP10481, TMEM5
Location	12q14.2
Gene ID	10329
Summary	Type II transmembrane protein with predicted glycosyltransferase function; mutations cause cobblestone lissencephaly, a severe brain malformation.