Gene: SPG21
Official Full Name: SPG21 abhydrolase domain containing, maspardinprovided by HGNC
Gene Summary: The protein encoded by this gene binds to the hydrophobic C-terminal amino acids of CD4 which are involved in repression of T cell activation. The interaction with CD4 is mediated by the noncatalytic alpha/beta hydrolase fold domain of this protein. It is thus proposed that this gene product modulates the stimulatory activity of CD4. Mutations in this gene are associated with autosomal recessive spastic paraplegia 21 (SPG21), also known as mast syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO22641 | SPG21 Knockout cell line (HeLa) | Human | SPG21 | 1:3~1:6 | Negative | Online Inquiry |
KO22642 | SPG21 Knockout cell line (HCT 116) | Human | SPG21 | 1:2~1:4 | Negative | Online Inquiry |
KO22643 | SPG21 Knockout cell line (HEK293) | Human | SPG21 | 1:3~1:6 | Negative | Online Inquiry |
KO22644 | SPG21 Knockout cell line (A549) | Human | SPG21 | 1:3~1:4 | Negative | Online Inquiry |
SPG21 Gene Knockout Cell Lines represent a specialized model system designed for the investigation of the SPG21 gene's role in human physiology and disease. By utilizing advanced CRISPR/Cas9 technology, these cell lines are engineered to lack functional SPG21, allowing researchers to elucidate the gene’s contribution to various biological pathways and neurodegenerative disorders, particularly those associated with hereditary spastic paraplegia.
The primary function of SPG21 Gene Knockout Cell Lines lies in their ability to mimic disease conditions in a controlled laboratory environment, enabling the functional characterization of the SPG21 gene. By observing the effects of knocking out the gene, researchers can gain insights into the molecular mechanisms underlying neurological dysfunction. These knockout models facilitate a deeper understanding of cellular processes such as apoptosis, autophagy, and mitochondrial dynamics, which are critically involved in neuronal health and disease progression.
The scientific importance of SPG21 Gene Knockout Cell Lines extends to their applications in both basic research and clinical settings. In research laboratories, these models are invaluable for studying gene function and validating potential therapeutic targets. Clinically, they offer a platform for high-throughput drug screening, allowing for the identification of novel compounds that could rectify SPG21-related pathologies, thereby impacting therapeutic strategies for patients.
One specific advantage of SPG21 Gene Knockout Cell Lines is their high specificity and reproducibility compared to traditional knockout methods, which often lead to off-target effects. Our cell lines are validated to ensure reliability in experimental outcomes, a crucial factor for researchers aiming for rigorous scientific results.
For researchers and clinicians focused on neurogenetic disorders, the SPG21 Gene Knockout Cell Lines are an essential tool that paves the way for breakthroughs in understanding and treating conditions linked to this gene. They provide a unique opportunity to explore the intricate relationship between gene expression and disease, potentially leading to innovative therapies.
Our company is dedicated to advancing the field of molecular biology through the development of cutting-edge research tools like the SPG21 Gene Knockout Cell Lines, bolstered by our commitment to high-quality standards and scientific excellence. We strive to support the research community in their quest for knowledge and therapeutic advancements.
Please note that all services are for research use only. Not intended for any clinical use.
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