Gene: SPOCK1
Official Full Name: SPARC (osteonectin), cwcv and kazal like domains proteoglycan 1provided by HGNC
Gene Summary: This gene encodes the protein core of a seminal plasma proteoglycan containing chondroitin- and heparan-sulfate chains. The protein's function is unknown, although similarity to thyropin-type cysteine protease-inhibitors suggests its function may be related to protease inhibition. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35251 | SPOCK1 Knockout cell line (HeLa) | Human | SPOCK1 | 1:3~1:6 | Negative | Online Inquiry |
KO35252 | SPOCK1 Knockout cell line (A549) | Human | SPOCK1 | 1:3~1:4 | Negative | Online Inquiry |
SPOCK1 Gene Knockout Cell Lines are specialized, genetically engineered cells in which the SPOCK1 gene has been disrupted or "knocked out" using advanced CRISPR-Cas9 technology. This targeted gene inactivation offers researchers a powerful tool to study the role of SPOCK1 in various biological processes, including cell adhesion, migration, and extracellular matrix interactions. By removing the function of this gene, scientists can effectively dissect its contributions to cellular behavior and investigate potential implications in diseases such as cancer and fibrosis.
The core mechanism behind these knockout cell lines relies on precise genomic editing, allowing researchers to investigate the phenotypic outcomes following SPOCK1 disruption. This facilitates a deeper understanding of the gene’s role in modulating cellular pathways and responses to environmental stimuli, thereby providing insights into pathophysiological mechanisms. In research settings, these cell lines are invaluable for exploring drug responses, gene interactions, and the underlying molecular mechanisms of disease.
What sets our SPOCK1 Gene Knockout Cell Lines apart from alternatives is the rigor of our validation processes. Each cell line is genetically characterized to ensure fidelity and reproducibility, reducing potential off-target effects commonly associated with gene editing. Researchers can have confidence in the robustness of their results, as these cell lines are optimized for various applications, including functional studies, therapeutic screenings, and mechanism elucidation.
This product is particularly attractive to researchers and clinicians focused on unraveling the complexities of cellular physiology and disease mechanisms. The ability to manipulate specific genes in a controlled manner allows for targeted investigations that can lead to novel therapeutic strategies or biomarker identification.
Our company has extensive expertise in gene editing technologies and a strong commitment to providing high-quality biological products. With a portfolio designed to meet the needs of the research community, we strive to empower scientists in their quest for innovative solutions in research and clinical applications.
Please note that all services are for research use only. Not intended for any clinical use.
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