Gene: SYNJ2
Official Full Name: synaptojanin 2provided by HGNC
Gene Summary: The gene is a member of the inositol-polyphosphate 5-phosphatase family. The encoded protein interacts with the ras-related C3 botulinum toxin substrate 1, which causes translocation of the encoded protein to the plasma membrane where it inhibits clathrin-mediated endocytosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO07903 | SYNJ2 Knockout cell line (HeLa) | Human | SYNJ2 | 1:3~1:6 | Negative | Online Inquiry |
KO07904 | SYNJ2 Knockout cell line (HCT 116) | Human | SYNJ2 | 1:2~1:4 | Negative | Online Inquiry |
KO07905 | SYNJ2 Knockout cell line (HEK293) | Human | SYNJ2 | 1:3~1:6 | Negative | Online Inquiry |
KO07906 | SYNJ2 Knockout cell line (A549) | Human | SYNJ2 | 1:3~1:4 | Negative | Online Inquiry |
SYNJ2 Gene Knockout Cell Lines are genetically modified cell lines designed specifically to investigate the functional roles of the SYNJ2 gene in cellular processes. By employing CRISPR/Cas9 technology, these cell lines exhibit a complete knockout of SYNJ2 expression, allowing researchers to study the biological consequences of its absence in a controlled environment. The SYNJ2 gene encodes a phosphoinositide phosphatase involved in synaptic vesicle recycling and membrane trafficking, making it particularly significant for understanding neurodegenerative diseases and synaptic dysfunctions.
The primary mechanism of action in these knockout cell lines centers on the loss of SYNJ2 protein, which disrupts normal lipid metabolism and vesicular transport activities. This alteration enables the exploration of various signaling pathways affected by the SYNJ2 protein, providing insights into its role in cellular homeostasis and synaptogenesis. Furthermore, researchers can utilize these models to identify potential therapeutic targets for diseases such as Alzheimer’s, where SYNJ2 is known to play a role.
The scientific importance of SYNJ2 Gene Knockout Cell Lines lies in their wide-ranging applications in both basic and translational research. These cell lines are invaluable for studying neurological function, drug discovery, and potential treatment strategies for synaptic-related disorders. Their ability to mimic human genetic mutations and offer insights into disease mechanisms makes them a critical resource for researchers and clinicians alike.
What sets SYNJ2 Gene Knockout Cell Lines apart is their precise and efficient knockout system, which ensures reproducibility and reliability in experimental outcomes. Compared to alternative methods, such as RNA interference, which may have off-target effects, the CRISPR/Cas9 approach provides a clean and definitive solution for gene editing.
For researchers and clinicians seeking to enhance their understanding of neurobiology, the SYNJ2 Gene Knockout Cell Lines are an essential tool. They allow for the delineation of complex biological interactions and pave the way for innovative therapeutic strategies. With a commitment to delivering high-quality biological products and unparalleled expertise in genetic modifications, our company ensures that researchers have access to the tools they need for groundbreaking discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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