Gene: STX2
Official Full Name: syntaxin 2provided by HGNC
Gene Summary: The product of this gene belongs to the syntaxin/epimorphin family of proteins. The syntaxins are a large protein family implicated in the targeting and fusion of intracellular transport vesicles. The product of this gene regulates epithelial-mesenchymal interactions and epithelial cell morphogenesis and activation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO38001 | STX2 Knockout cell line (HeLa) | Human | STX2 | 1:3~1:6 | Negative | Online Inquiry |
KO38002 | STX2 Knockout cell line (HCT 116) | Human | STX2 | 1:2~1:4 | Negative | Online Inquiry |
KO38003 | STX2 Knockout cell line (HEK293) | Human | STX2 | 1:3~1:6 | Negative | Online Inquiry |
KO38004 | STX2 Knockout cell line (A549) | Human | STX2 | 1:3~1:4 | Negative | Online Inquiry |
STX2 Gene Knockout Cell Lines are genetically engineered cell lines that have been developed to lack the syntaxin 2 (STX2) gene, a member of the syntaxin family essential for various membrane trafficking processes. By specifically employing CRISPR/Cas9 technology or similar gene-editing techniques, these cell lines allow researchers to investigate the role of STX2 in cellular functions such as vesicle fusion, neurotransmitter release, and hormone secretion.
The primary mechanism of action revolves around the deletion of the STX2 gene, which disrupts the normal molecular pathways involved in exocytosis and intracellular communication. This provides a valuable model for studying diseases where STX2 dysfunction may be implicated, including certain neuropsychiatric disorders and cancer. Researchers can explore how the absence of STX2 impacts cellular behavior, signaling pathways, and physiological responses, enabling the identification of potential therapeutic targets.
The scientific importance of STX2 Gene Knockout Cell Lines lies in their versatility and applicability in both basic research and clinical contexts. They can be utilized to elucidate the molecular mechanisms underlying various diseases, facilitate drug discovery, and assist in the validation of biomarkers. Moreover, these knockout cell lines can play a critical role in developing targeted therapies, offering insights into how specific genetic alterations influence drug response and resistance.
One significant advantage of the STX2 Gene Knockout Cell Lines is their high specificity and reproducibility, allowing for consistent results that enhance the reliability of experimental outcomes. Compared to other genetic modification approaches, such as RNA interference, gene knockout provides a more permanent alteration of gene expression, enabling long-term studies of gene function.
Researchers and clinicians will find STX2 Gene Knockout Cell Lines invaluable for advancing understanding of synaptic transmission and other cellular processes linked to STX2, potentially translating into innovative treatment strategies. With extensive expertise in genetic engineering and cell line development, our company offers superior quality biological products tailored to meet the rigorous demands of the biotech and pharmaceutical industries, thereby enhancing research efficacy and outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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