Gene: KDSR
Official Full Name: 3-ketodihydrosphingosine reductaseprovided by HGNC
Gene Summary: The protein encoded by this gene catalyzes the reduction of 3-ketodihydrosphingosine to dihydrosphingosine. The putative active site residues of the encoded protein are found on the cytosolic side of the endoplasmic reticulum membrane. A chromosomal rearrangement involving this gene is a cause of follicular lymphoma, also known as type II chronic lymphatic leukemia. The mutation of a conserved residue in the bovine ortholog causes spinal muscular atrophy. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO37785 | KDSR Knockout cell line (HeLa) | Human | KDSR | 1:3~1:6 | Negative | Online Inquiry |
KO37786 | KDSR Knockout cell line (HCT 116) | Human | KDSR | 1:2~1:4 | Negative | Online Inquiry |
KO37787 | KDSR Knockout cell line (HEK293) | Human | KDSR | 1:3~1:6 | Negative | Online Inquiry |
KO37788 | KDSR Knockout cell line (A549) | Human | KDSR | 1:3~1:4 | Negative | Online Inquiry |
KDSR Gene Knockout Cell Lines are specifically engineered human cell lines that possess a targeted disruption of the KDSR gene, crucial for the biosynthesis of lysine-derived sphingolipids. This genetic modification allows for comprehensive studies into the role of KDSR in various biological processes, such as cellular membrane dynamics, apoptosis, and cell signaling pathways. The loss of KDSR function presents a unique opportunity for researchers to explore the implications of altered sphingolipid metabolism and its association with numerous pathological conditions, including cancer, neurodegenerative diseases, and metabolic disorders.
The mechanisms underlying the functionality of KDSR Gene Knockout Cell Lines hinge upon CRISPR-Cas9 gene editing technology, which provides a precise and efficient means for gene disruption. This level of specificity ensures that any observed phenotypic changes are attributable solely to the lack of KDSR activity, thereby facilitating accurate experimental outcomes. Furthermore, these cell lines can be utilized in pharmacological studies to test new therapeutics aimed at modulating sphingolipid metabolism, providing valuable insights into their efficacy and mechanisms of action.
Scientifically, KDSR Gene Knockout Cell Lines hold significant importance in both research and clinical applications. In the lab, they serve as a robust model for elucidating the biochemical pathways regulated by KDSR, enabling researchers to identify potential biomarkers for disease states. Clinically, understanding the role of KDSR could lead to novel therapeutic targets, paving the way for innovative treatments that could improve patient outcomes.
The advantages of KDSR Gene Knockout Cell Lines over traditional models lie in their reproducibility and the precision of the gene knockout. Unlike broader knockout models or pharmacological inhibitors, these cell lines afford researchers the ability to study the inherent biological effects of KDSR loss in a controlled environment. Furthermore, they are fully characterized and optimized for a range of applications, providing a reliable resource for experimental reproducibility.
For researchers and clinicians aiming to deepen their understanding of sphingolipid-related biology, KDSR Gene Knockout Cell Lines represent a critical tool. Our company is dedicated to advancing scientific research by providing high-quality, rigorously validated biological products, ensuring that researchers have access to the best tools for groundbreaking discoveries in cellular and molecular biology.
Please note that all services are for research use only. Not intended for any clinical use.
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