Gene: POMGNT1
Official Full Name: protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)provided by HGNC
Gene Summary: This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Feb 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00973 | POMGNT1 Knockout cell line (HCT 116) | Human | POMGNT1 | Negative | Online Inquiry | |
KO14973 | POMGNT1 Knockout cell line (HeLa) | Human | POMGNT1 | 1:3~1:6 | Negative | Online Inquiry |
KO14974 | POMGNT1 Knockout cell line (HEK293) | Human | POMGNT1 | 1:3~1:6 | Negative | Online Inquiry |
KO14975 | POMGNT1 Knockout cell line (A549) | Human | POMGNT1 | 1:3~1:4 | Negative | Online Inquiry |
POMGNT1 Gene Knockout Cell Lines represent a cutting-edge biological research tool designed for studying the role of the POMGNT1 gene in cellular processes and disease pathways. These cell lines have been genetically engineered to disrupt the normal expression of the POMGNT1 gene, which is crucial for glycosylation processes involved in muscle and neurological functions. By creating a knockout model, researchers can elucidate the specific contributions of POMGNT1 to the development of congenital disorders, including muscle dystrophies and other glycosylation-related diseases.
The key mechanism by which these cell lines function lies in the targeted gene editing techniques, such as CRISPR-Cas9 or similar technologies, effectively causing a sequence alteration that inhibits the expression of the POMGNT1 protein. This functional disruption allows for comprehensive analyses of the phenotypic outcomes, signaling pathways, and cellular behaviors that are affected by the loss of POMGNT1, providing invaluable insights into the gene's role in health and disease.
In both research and clinical settings, the POMGNT1 Gene Knockout Cell Lines are instrumental for advancing our understanding of glycosylation and its association with various pathologies. They serve as essential tools for drug discovery, biomarker identification, and the exploration of novel therapeutic strategies targeting glycosylation defects. Given the ongoing research into rare diseases that stem from glycosylation anomalies, these cell lines are particularly relevant for biopharmaceutical applications.
Compared to alternative cell lines, the POMGNT1 knockout models offer the unique advantage of enabling precise, targeted studies on a gene that is pivotal in a specialized area of molecular biology. Their specificity facilitates higher accuracy in experimental outcomes, ensuring robust and reproducible results that are critical for scientific advancement.
In conclusion, the POMGNT1 Gene Knockout Cell Lines provide invaluable resources for researchers and clinicians seeking to deepen their understanding of glycosylation and its implications in health and disease. Our company specializes in creating high-quality genetic models, leveraging state-of-the-art technologies to support advancements in biomedical research and foster innovation in therapeutic development.
Please note that all services are for research use only. Not intended for any clinical use.
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