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ALG3 Knockout Cell Lines

Gene: ALG3

Official Full Name: ALG3 alpha-1,3- mannosyltransferaseprovided by HGNC

Gene Summary: This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO32170 ALG3 Knockout cell line (HeLa) Human ALG3 1:3~1:6 Negative Online Inquiry
KO32171 ALG3 Knockout cell line (HCT 116) Human ALG3 1:2~1:4 Negative Online Inquiry
KO32172 ALG3 Knockout cell line (HEK293) Human ALG3 1:3~1:6 Negative Online Inquiry
KO32173 ALG3 Knockout cell line (A549) Human ALG3 1:3~1:4 Negative Online Inquiry

Background

ALG3 Gene Knockout Cell Lines are a cutting-edge tool designed for the study of glycosylation processes and the biological implications of defective glycan synthesis. The ALG3 gene encodes a key enzyme involved in the early stages of N-glycosylation, specifically catalyzing the addition of the first glucose residue to the growing oligosaccharide chain on nascent glycoproteins. By creating knockout cell lines that lack functional ALG3 expression, researchers can elucidate the role of this gene in glycan formation and its downstream effects on protein maturation and stability.

The primary function of ALG3 Gene Knockout Cell Lines lies in their ability to serve as a model for studying glycosylation-related disorders and the cellular responses to altered glycoprotein profiles. The knockout mechanism disrupts the normal glycosylation pathway, enabling the examination of the resulting phenotypic changes, which can include altered cellular signaling, protein misfolding, and impacts on cell proliferation. These insights are crucial in understanding the basis of various congenital disorders of glycosylation and other related diseases.

The scientific importance of these cell lines can be observed in both research and clinical contexts, where they provide a valuable platform for drug discovery, biomarker development, and the study of therapeutic approaches targeting glycosylation pathways. Their application in high-throughput screening can accelerate the identification of compounds that modulate glycosylation patterns, offering new avenues in disease treatment.

Compared to traditional cell lines utilized in similar studies, ALG3 Gene Knockout Cell Lines provide a more specific and relevant model for glycosylation research. Unlike other knockout models, these lines meticulously replicate the alteration at a crucial juncture in the glycosylation pathway, yielding findings that are predicted to be more reflective of physiological processes. This specificity enhances the precision of research outcomes, thereby improving reproducibility and applicability.

For researchers and clinicians, the value proposition of ALG3 Gene Knockout Cell Lines is compelling. They offer a unique resource for elucidating the complexities of glycoprotein maturation and its implications in disease, facilitating a deeper understanding of therapeutic targets. Furthermore, they empower users to push the boundaries of current glycosylation research.

Our company boasts extensive expertise in the development of high-quality biological products tailored for your research needs. With a commitment to innovation and supporting scientific discovery, we provide unparalleled resources that enable advancements in the 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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