Gene: DTNBP1
Official Full Name: dystrobrevin binding protein 1provided by HGNC
Gene Summary: This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. A similar protein in mouse is a component of a protein complex termed biogenesis of lysosome-related organelles complex 1 (BLOC-1), and binds to alpha- and beta-dystrobrevins, which are components of the dystrophin-associated protein complex (DPC). Mutations in this gene are associated with Hermansky-Pudlak syndrome type 7. This gene may also be associated with schizophrenia. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO02222 | DTNBP1 Knockout cell line (HeLa) | Human | DTNBP1 | 1:3~1:6 | Negative | Online Inquiry |
KO02223 | DTNBP1 Knockout cell line (HCT 116) | Human | DTNBP1 | 1:2~1:4 | Negative | Online Inquiry |
KO02224 | DTNBP1 Knockout cell line (HEK293) | Human | DTNBP1 | 1:3~1:6 | Negative | Online Inquiry |
KO02225 | DTNBP1 Knockout cell line (A549) | Human | DTNBP1 | 1:3~1:4 | Negative | Online Inquiry |
DTNBP1 Gene Knockout Cell Lines represent a powerful tool in genetic research and biomedicine, meticulously engineered to eliminate the expression of the DTNBP1 gene. The DTNBP1 gene encodes a protein crucial for synaptic vesicle dynamics, and its dysregulation has been implicated in various neuropsychiatric disorders, including schizophrenia and bipolar disorder. By creating these knockout cell lines, researchers can investigate the role of DTNBP1 in cellular processes, neuronal function, and disease pathogenesis, allowing for a clearer understanding of its contribution to brain disorders.
The primary function of DTNBP1 Gene Knockout Cell Lines lies in their ability to provide a controlled environment to observe the absence of DTNBP1 protein, thereby elucidating its biological pathways and interactions. The mechanism relies on CRISPR-Cas9 gene-editing technology, which facilitates precise modifications in the genomic sequence, leading to the stable knockout of the gene. This level of control helps in dissecting the gene's involvement in neurotransmitter release and synaptic transmission, critical elements of neurobiology.
Scientific investigations utilizing DTNBP1 knockout models have applications in drug discovery, pathway elucidation, and personalized medicine approaches. The relevance of this knockout model extends to studies of neurodevelopmental and mood disorders, making it invaluable for both academia and pharmaceutical research. Its application can significantly enhance the translational potential of findings from bench to bedside, providing critical insights into potential therapeutic targets.
Compared to alternative models, DTNBP1 Gene Knockout Cell Lines offer high specificity and reproducibility. They allow for real-time monitoring of cellular responses without the interference that other methods may introduce, such as chemical inhibitors or siRNA-based knockdown techniques that can produce off-target effects or temporary changes in gene expression.
For researchers and clinicians aiming to explore the nuances of neuropsychiatric disorders, the DTNBP1 Gene Knockout Cell Lines provide an essential platform that bridges gaps in our understanding of disease etiology and treatment. Our company is dedicated to advancing research through innovative biological products, utilizing state-of-the-art technologies and a commitment to quality and precision in every offering, ensuring that our customers receive tools that empower impactful discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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