Gene: DPM3
Official Full Name: dolichyl-phosphate mannosyltransferase subunit 3, regulatoryprovided by HGNC
Gene Summary: Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of mannosyl residues on the lumenal side of the endoplasmic reticulum (ER). Lack of Dol-P-Man results in defective surface expression of GPI-anchored proteins. Dol-P-Man is synthesized from GDP-mannose and dolichol-phosphate on the cytosolic side of the ER by the enzyme dolichyl-phosphate mannosyltransferase. The protein encoded by this gene is a subunit of dolichyl-phosphate mannosyltransferase and acts as a stabilizer subunit of the dolichyl-phosphate mannosyltransferase complex. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO21807 | DPM3 Knockout cell line (HeLa) | Human | DPM3 | 1:3~1:6 | Negative | Online Inquiry |
KO21808 | DPM3 Knockout cell line (HCT 116) | Human | DPM3 | 1:2~1:4 | Negative | Online Inquiry |
KO21809 | DPM3 Knockout cell line (HEK293) | Human | DPM3 | 1:3~1:6 | Negative | Online Inquiry |
KO21810 | DPM3 Knockout cell line (A549) | Human | DPM3 | 1:3~1:4 | Negative | Online Inquiry |
DPM3 Gene Knockout Cell Lines are specialized cell lines that have been genetically engineered to disrupt the expression of the DPM3 gene, which plays a crucial role in the synthesis of dolichol phosphate. Dolichol phosphate is vital for N-glycosylation, a post-translational modification essential for proper protein folding and function. By targeting the DPM3 gene, these knockout cell lines serve as powerful tools for elucidating the biological pathways associated with glycoprotein synthesis and identifying the consequences of disrupted glycosylation patterns.
The key mechanism underlying the functionality of DPM3 Gene Knockout Cell Lines involves the inactivation of DPM3, which leads to reduced levels of dolichol phosphate and subsequent impairment in glycosylation processes. This can result in altered protein localization, stability, and activity, providing researchers with a valuable experimental model to study the implications of glycosylation deficiencies in various physiological and pathological contexts, including cancer progression, congenital disorders, and targeted drug delivery mechanisms.
The scientific importance of these cell lines extends into both research and clinical settings. In research, they enable the exploration of glycosylation's role in cellular signaling and development, while in clinical studies, such models can assist in understanding patient-specific glycosylation patterns that may affect disease outcomes and treatment responses. Additionally, the use of DPM3 Gene Knockout Cell Lines can facilitate drug discovery efforts aimed at correcting glycosylation defects or identifying new therapeutic targets.
What sets DPM3 Gene Knockout Cell Lines apart from alternatives is their specificity and reliability, derived from precise gene-editing techniques such as CRISPR-Cas9. These cell lines exhibit consistent and reproducible phenotypic outcomes, thereby enhancing experimental rigor and ensuring that results are reflective of genuine biological processes rather than artifacts of in vitro culture systems.
For researchers and clinicians alike, the DPM3 Gene Knockout Cell Lines present an invaluable resource, providing insights that could lead to breakthroughs in understanding glycosylation-related diseases and optimizing therapeutic strategies. Partnering with our company, known for its commitment to precision genetic engineering and high-quality biological products, gives you access to advanced tools that support your innovative research initiatives and clinical applications.
Please note that all services are for research use only. Not intended for any clinical use.
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