Gene: SYAP1
Official Full Name: synapse associated protein 1provided by HGNC
Gene Summary: Involved in several processes, including TORC2 signaling; cellular response to epidermal growth factor stimulus; and cellular response to peptide hormone stimulus. Located in several cellular components, including Golgi apparatus; cytoplasmic side of plasma membrane; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO22089 | SYAP1 Knockout cell line (HeLa) | Human | SYAP1 | 1:3~1:6 | Negative | Online Inquiry |
KO22090 | SYAP1 Knockout cell line (HCT 116) | Human | SYAP1 | 1:2~1:4 | Negative | Online Inquiry |
KO22091 | SYAP1 Knockout cell line (HEK293) | Human | SYAP1 | 1:3~1:6 | Negative | Online Inquiry |
KO22092 | SYAP1 Knockout cell line (A549) | Human | SYAP1 | 1:3~1:4 | Negative | Online Inquiry |
SYAP1 Gene Knockout Cell Lines are a specialized set of genetically modified cell lines in which the SYAP1 gene has been inactivated, allowing for the comprehensive study of its functional role within various biological processes. SYAP1, or Synapse Associated Protein 1, is known to be a critical component in the formation and maintenance of synapses, making these cell lines invaluable for research pertaining to neurobiology, cellular signaling, and synaptic function.
These knockout cell lines operate on a foundational mechanism of gene editing, commonly utilizing CRISPR/Cas9 technology, which precisely induces double-strand breaks in the DNA sequence coding for SYAP1. The resulting repair process via non-homologous end joining leads to the disruption of the gene, effectively rendering it non-functional. This allows researchers to investigate the loss-of-function effects of SYAP1 within a controlled environment, providing insights into pathways influenced by this protein, including potential implications in neurological disorders.
The scientific importance of SYAP1 Gene Knockout Cell Lines extends into both research and clinical settings. In research, these cell lines are pivotal for elucidating mechanisms underlying synaptic plasticity and neurodevelopmental disorders. Clinically, insights gained through using these models may contribute to targeted therapies for conditions such as autism spectrum disorders and schizophrenia, where synaptic dysfunction is highlighted.
Compared to alternative models, such as siRNA knockdowns or overexpression systems, the SYAP1 Gene Knockout Cell Lines offer a more stable and complete loss-of-function context, leading to more reproducible and reliable data. Furthermore, the permanence of the knockout allows for long-term studies that correlate cellular behavior with observed phenotypic changes, addressing the depth of research required in genetic studies.
For researchers, clinicians, and pharmaceutical companies seeking to advance their understanding of synaptic mechanisms and develop innovative treatments, investing in SYAP1 Gene Knockout Cell Lines presents a unique opportunity to drive impactful discoveries. Our company, a leader in providing high-quality biological products, is committed to ensuring that you have access to the latest advancements in genetic research tools, setting a solid foundation for your discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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