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GlycoErase™ GALNT1 Knockout Human Skin Cancer Cell A2058

CAT#: GLJF-0525-JF923

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Overview
Description
The GALNT1 knockout A2058 cell line, lacking polypeptide N-acetylgalactosaminyltransferase 1 that initiates muciN-type O-glycosylation, allows for the investigation of muciN-type O-glycosylation's role in melanoma, potentially affecting cell surface properties, cell-cell interactions, and barrier functions relevant to tumor behavior.
Product Type
KO Cell Lines
Species
Human
Cell Morphology
Epithelial cells, adherent
Passage Ratio
1:2~1:3
Cell Line
A2058
Primary Disease
Melanoma
Lineage
Skin
Specification
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
EMEM & 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 Information
Target
GALNT1
Full Name
Polypeptide N-acetylgalactosaminyltransferase 1
Alternative Name
GalNAc-T1
Location
18q12.2
Gene ID
Summary
Initiates mucin-type O-linked glycosylation by transferring GalNAc to serine and threonine residues on target proteins within the Golgi apparatus.
For Research Use Only.
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