Gene: SPEF1
Official Full Name: sperm flagellar 1provided by HGNC
Gene Summary: Enables actin binding activity. Involved in filopodium assembly and lamellipodium assembly. Located in several cellular components, including basolateral plasma membrane; lamellipodium; and microvillus. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO28695 | SPEF1 Knockout cell line (HCT 116) | Human | SPEF1 | 1:2~1:4 | Negative | Online Inquiry |
SPEF1 Gene Knockout Cell Lines are an advanced biotechnological tool designed to facilitate the study of the SPEF1 gene, known for its involvement in the development and maintenance of cilia and flagella in various cell types. By employing CRISPR-Cas9 technology, these cell lines allow for precise gene editing, resulting in the complete knockout of SPEF1 function. This targeted approach enables researchers to investigate the consequential phenotypic effects linked to SPEF1 deficiencies, thus unraveling its role in critical biological processes.
The key function of these knockout cell lines lies in their ability to provide a controlled environment for assessing the impacts of the SPEF1 gene on cellular behavior. Researchers can conduct assays to measure changes in motility, proliferation, and cilia structure, offering insights that are crucial for understanding the underlying mechanisms of ciliary dysfunctions associated with various diseases, including respiratory disorders and infertility conditions.
In terms of scientific significance, SPEF1 Gene Knockout Cell Lines are invaluable in both basic and clinical research. They serve as models for studying genetic diseases, evaluating therapeutic effects, or screening potential drug candidates targeting ciliary-related pathologies. Furthermore, they aid in elucidating the molecular pathways involving SPEF1, thus contributing to the wider field of regenerative medicine.
Compared to alternative models, such as wild-type cell lines or non-targeted knockout approaches, these specialized cell lines provide a higher specificity and reliability, ensuring that experimental outcomes can be directly attributed to the absence of the SPEF1 gene. Additionally, their consistency in genetic background allows for reproducible research findings, enhancing the robustness of scientific inquiry.
Researchers and clinicians looking to deepen their understanding of motile cilia-related diseases will find significant value in SPEF1 Gene Knockout Cell Lines. By providing an accurate and well-characterized model, these cell lines not only open new avenues of research but also facilitate the development of potential therapeutic strategies.
Backed by our company’s extensive expertise in genetic engineering and cellular models, we are committed to offering high-quality biological products that meet the rigorous demands of contemporary scientific research.
Please note that all services are for research use only. Not intended for any clinical use.
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