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ST3GAL2 Knockout Cell Lines

Gene: ST3GAL2

Official Full Name: ST3 beta-galactoside alpha-2,3-sialyltransferase 2provided by HGNC

Gene Summary: The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi but can be proteolytically processed to a soluble form. This protein, which is a member of glycosyltransferase family 29, can use the same acceptor substrates as does sialyltransferase 4A. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35428 ST3GAL2 Knockout cell line (HeLa) Human ST3GAL2 1:3~1:6 Negative Online Inquiry
KO35429 ST3GAL2 Knockout cell line (HCT 116) Human ST3GAL2 1:2~1:4 Negative Online Inquiry
KO35430 ST3GAL2 Knockout cell line (HEK293) Human ST3GAL2 1:3~1:6 Negative Online Inquiry
KO35431 ST3GAL2 Knockout cell line (A549) Human ST3GAL2 1:3~1:4 Negative Online Inquiry

Background

ST3GAL2 Gene Knockout Cell Lines are specialized, genetically engineered cell lines that have undergone targeted mutagenesis to disrupt the ST3GAL2 gene, which encodes for an enzyme responsible for the synthesis of polysialic acid (PSA) on glycoproteins and glycolipids. These knockout cell lines are invaluable tools for studying the functional implications of ST3GAL2 absence in cellular processes, particularly in the context of developmental biology, cancer research, and neurobiology.

The primary function of ST3GAL2 in cellular mechanisms involves the modification of cell surface proteins, which influences cell-cell interactions, signaling pathways, and the development of cellular adhesion features. By facilitating the addition of sialic acid moieties to glycoproteins, ST3GAL2 plays a crucial role in modulating immune responses and neuronal development. The knockout of this gene allows researchers to elucidate the role of PSA in processes like neuronal plasticity, tumor progression, and cell signaling pathways, thereby contributing to a deeper understanding of how sialylation impacts physiological and pathological conditions.

In research and clinical settings, ST3GAL2 Gene Knockout Cell Lines are instrumental in providing insights into diseases linked to aberrant glycosylation, including various cancers and neurodegenerative disorders. By utilizing these cell lines, researchers can explore alternative therapeutic strategies aimed at targeting sialylation processes, potentially paving the way for novel interventions and improving clinical outcomes.

What sets ST3GAL2 Gene Knockout Cell Lines apart from traditional cellular models is their precision and specificity; they enable the investigation of the direct effects of the ST3GAL2 gene's absence, rather than relying on indirect inference, thus yielding more reliable and reproducible results. Furthermore, these models are valuable for validating findings from heterogeneous systems or animal models, allowing for a more streamlined path toward translational research.

In light of these compelling advantages, ST3GAL2 Gene Knockout Cell Lines serve as a crucial asset for researchers and clinicians seeking to innovate in the fields of glycoscience and disease mechanism discovery. Backed by a team of experts in genetic engineering and molecular biology, our company is committed to providing high-quality biological products that advance scientific research and enhance our understanding of complex biological systems.

Please note that all services are for research use only. Not intended for any clinical use.

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