Gene: SOBP
Official Full Name: sine oculis binding protein homologprovided by HGNC
Gene Summary: The protein encoded by this gene is a nuclear zinc finger protein that is involved in development of the cochlea. Defects in this gene have also been linked to intellectual disability. [provided by RefSeq, Mar 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO13852 | SOBP Knockout cell line (HCT 116) | Human | SOBP | 1:2~1:4 | Negative | Online Inquiry |
KO13853 | SOBP Knockout cell line (HEK293) | Human | SOBP | 1:3~1:6 | Negative | Online Inquiry |
SOBP Gene Knockout Cell Lines are specifically engineered cell lines in which the SRY-Box Transcription Factor 2 (SOBP) gene has been completely inactivated through advanced gene editing techniques such as CRISPR/Cas9. These cell lines provide a robust platform for investigating the role of the SOBP gene in various biological processes, including cell differentiation, proliferation, and neurodevelopmental pathways. By removing the influence of SOBP, researchers can pinpoint its functional contributions, thereby enhancing our understanding of gene regulation and expression.
The primary function of these knockout cell lines is to facilitate the study of gene loss-of-function effects. By observing the resultant phenotypical and molecular changes, researchers can elucidate the pathways influenced by SOBP under specific conditions, providing insights into associated disorders, particularly in neural contexts where SOBP is implicated. These models are invaluable in research settings focused on developmental biology, neurology, and gene expression regulation, allowing for a more nuanced exploration of cellular mechanisms.
The scientific importance of SOBP Gene Knockout Cell Lines lies in their ability to act as a translational tool for understanding the role of transcription factors in development and diseases, such as schizophrenia or autism spectrum disorders. Their use in drug discovery and disease modeling can pave the way for innovative therapeutic interventions.
When compared to alternative gene editing approaches, these knockout cell lines are advantageous due to their specificity and reproducibility. Researchers benefit from the ability to generate consistent, high-quality data and to perform experiments across various conditions without the confounding effects of the SOBP gene.
For researchers and clinicians committed to advancing their understanding of genetic disturbances and developing targeted therapies, SOBP Gene Knockout Cell Lines represent an indispensable asset. Their precision enables enhanced research accuracy, leading to faster breakthroughs in gene function elucidation.
Our company excels in delivering biologically relevant tools and resources, ensuring that innovators have access to quality models like the SOBP Gene Knockout Cell Lines for their cutting-edge research and clinical applications.
Please note that all services are for research use only. Not intended for any clinical use.
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