Gene: ST6GAL1
Official Full Name: ST6 beta-galactoside alpha-2,6-sialyltransferase 1provided by HGNC
Gene Summary: This gene encodes a member of glycosyltransferase family 29. The encoded protein is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The protein, which is normally found in the Golgi but can be proteolytically processed to a soluble form, is involved in the generation of the cell-surface carbohydrate determinants and differentiation antigens HB-6, CD75, and CD76. This gene has been incorrectly referred to as CD75. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03727 | ST6GAL1 Knockout cell line (HCT 116) | Human | ST6GAL1 | 1:2~1:4 | Negative | Online Inquiry |
KO03728 | ST6GAL1 Knockout cell line (HEK293) | Human | ST6GAL1 | 1:3~1:6 | Negative | Online Inquiry |
KO03729 | ST6GAL1 Knockout cell line (A549) | Human | ST6GAL1 | 1:3~1:4 | Negative | Online Inquiry |
ST6GAL1 Gene Knockout Cell Lines are specialized cellular models designed to facilitate the study of ST6 β-galactosamine α-2,6-sialyltransferase 1, a critical enzyme involved in the sialylation of glycoproteins and glycolipids. Sialylation is a vital biochemical modification that influences cell-cell interactions, immune response, and tumor progression. These knockout cell lines are generated using advanced CRISPR-Cas9 technology, enabling precise and efficient disruption of the ST6GAL1 gene. As a result, researchers can meticulously examine the downstream effects of ST6GAL1 deficiency on cellular behavior, signaling pathways, and overall cellular function.
The unique functionality of these cell lines lies in their ability to serve as robust tools for dissecting the role of sialylation in various biological contexts, including cancer biology, immunology, and developmental studies. By simulating a loss-of-function condition, scientists can gain insights into how alterations in the sialylation process affect glycan-mediated interactions, which are known to play pivotal roles in maintaining homeostasis and disease progression.
The scientific importance of ST6GAL1 Gene Knockout Cell Lines in research cannot be overstated. These cellular models are invaluable in preclinical studies, enabling the exploration of novel therapeutic targets for diseases such as cancer and autoimmune disorders. They allow researchers to evaluate the effectiveness of sialic acid-targeting therapies and understand the implications of glycan modifications in disease states.
Compared to standard cell lines, these knockout models provide a level of specificity and fidelity that enhances experimental outcomes. Researchers benefit from their ability to focus on the direct impacts of ST6GAL1 absence without confounding variables, ultimately leading to more reliable data. Furthermore, the ease of use and reproducibility associated with these cell lines significantly lowers the barrier to exploration in sialylation-related research.
In conclusion, ST6GAL1 Gene Knockout Cell Lines represent a cutting-edge platform for scientists aiming to unravel the complexities of sialylation. Backed by our company's extensive expertise in genetic engineering and cell line development, we are committed to providing high-quality, validated tools that empower advances in biomedical research. Our products are designed to meet the growing demands of modern scientific inquiry, making them an essential addition to any laboratory focused on glycoscience and its implications in health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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