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Species | Human |
Cat.No | ABC-KH10105 |
Product Category | Transfected Stable Cell Lines |
Size/Quantity | 1 vial |
Shipping Info | Dry Ice |
Growth Conditions | 37 ℃, 5% CO2 |
Biosafety Level | 1 |
Storage | Liquid Nitrogen |
Product Type | Knockout Stable Cell Line |
Host Cell | HEK293; HeLa or other cell lines |
Human NINJ1 knockout cell line is edited by CRISPR/Cas9 technology.
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ll give you a $100 coupon. Simply click here and submit your paper’s PubMed ID (PMID).
For research use only
The Human NINJ1 Knockout Cell Line is a genetically engineered cell line where the NINJ1 gene has been disrupted or “knocked out” using CRISPR/Cas9 technology. This allows researchers to study the function of the NINJ1 gene by observing the effects of its absence on cellular processes.
This cell line is created using CRISPR/Cas9 technology, a precise genome-editing tool that enables the targeted disruption of the NINJ1 gene. This results in the complete knockout of the gene, allowing for detailed studies of its role and function in various cellular processes.
The Human NINJ1 Knockout Cell Line is used to investigate the biological functions and pathways involving the NINJ1 gene. It is valuable for studying neural regeneration, cell adhesion, inflammation, blood-brain barrier integrity, and apoptosis. These studies can contribute to the understanding of neurological and immunological diseases and the development of new therapeutic approaches.
The NINJ1 gene plays crucial roles in several biological processes, including neural regeneration, cell adhesion, and immune response regulation. By studying the effects of NINJ1 knockout, researchers can gain insights into its function and involvement in disease mechanisms, potentially leading to new therapeutic targets for neurological and immune-related conditions.
CRISPR/Cas9-edited Human NINJ1 Knockout Cell Line offers several advantages, including high specificity and efficiency in gene editing, allowing for precise disruption of the NINJ1 gene. This facilitates the study of gene function and interaction in a controlled environment, providing reliable data for understanding NINJ1’s role in cellular processes and disease states.