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GlycoErase™ RXYLT1 Knockout Human Ovarian Cancer Cell A2780 (CAT#: GLJF-0525-JF1101)

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1 M cells/vial*2

Description RXYLT1 knockout A2780 cells, deficient in ribitol xylosyltransferase 1 predicted to have glycosyltransferase function, enable study of glycosyltransferase function disruption, potentially affecting unknown glycosylation pathways and requiring further research to define RXYLT1's role.
Product Type KO Cell Lines
Species Human
Cell Morphology Epithelial-like, adherent
Passage Ratio 1:3~1:6
Cell Line A2780
Primary Disease Ovarian Epithelial Tumor
Lineage Ovary/Fallopian Tube
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 FBS & Glutamine & 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 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.
For Research Use Only.
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