Gene: SPG7
Official Full Name: SPG7 matrix AAA peptidase subunit, parapleginprovided by HGNC
Gene Summary: This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2014]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO13794 | SPG7 Knockout cell line (HeLa) | Human | SPG7 | 1:3~1:6 | Negative | Online Inquiry |
KO13795 | SPG7 Knockout cell line (HCT 116) | Human | SPG7 | 1:2~1:4 | Negative | Online Inquiry |
KO13796 | SPG7 Knockout cell line (HEK293) | Human | SPG7 | 1:3~1:6 | Negative | Online Inquiry |
KO13797 | SPG7 Knockout cell line (A549) | Human | SPG7 | 1:3~1:4 | Negative | Online Inquiry |
SPG7 Gene Knockout Cell Lines are sophisticated biological tools engineered to facilitate the study of the SPG7 gene, which plays a crucial role in cellular function and neurodegenerative disorders. The SPG7 gene encodes the serine protease-like protein, involved in mitochondrial dynamics and apoptosis regulation. The knockout cell lines provide a specialized platform for researchers to investigate the biological pathways associated with SPG7 and their implications in conditions such as hereditary spastic paraplegia.
These cell lines operate through a targeted gene disruption approach, utilizing CRISPR-Cas9 technology to create precise deletions or modifications within the SPG7 gene sequence. This mechanism allows for the detailed exploration of gene function, protein interactions, and the downstream effects of its absence on cellular behavior, metabolism, and signaling pathways. Researchers can employ various assays to elucidate the phenotypic consequences of SPG7 deletion, gaining insights into its role in mitochondrial function and neurological health.
The scientific importance of SPG7 Gene Knockout Cell Lines lies in their capacity to advance understanding in both fundamental biology and potential therapeutic interventions. Their utility spans across basic research, drug discovery, and the development of gene therapies, addressing unmet needs in regenerative medicine and genetic disorders.
One of the key advantages of our SPG7 Gene Knockout Cell Lines is the rigorous validation process that ensures the fidelity and reproducibility of the knockout. Unlike alternative models, which may produce inconsistent results, these cell lines offer reliable outcomes, critical for researchers aiming for a deeper understanding of SPG7-associated pathologies. Additionally, our product is designed for ease of use, with optimized growth conditions that facilitate efficient handling and experimentation.
We believe that our SPG7 Gene Knockout Cell Lines are invaluable assets to researchers and clinicians committed to unraveling the complexities of neurodegenerative diseases and developing novel therapeutic strategies. Backed by a team of experts and a history of innovation in biological products, we are dedicated to providing tools that enhance scientific discovery and improve health outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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