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TOR1B Knockout Cell Lines

Gene: TOR1B

Official Full Name: torsin family 1 member Bprovided by HGNC

Gene Summary: The protein encoded by this gene is an ATPase found primarily in the endoplasmic reticulum and nuclear envelope. This gene has a highly-similar neighboring gene, TOR1A, that encodes a protein that is likely to interact in a complex with this protein. Finally, this protein may act as a chaperone and play a role in maintaining the integrity of the nuclear envelope and endoplasmic reticulum. Several transcript variants, some protein-coding and others non-protein coding, have been found for this gene. [provided by RefSeq, Dec 2015]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO27616 TOR1B Knockout cell line (HeLa) Human TOR1B 1:3~1:6 Negative Online Inquiry
KO27617 TOR1B Knockout cell line (HCT 116) Human TOR1B 1:2~1:4 Negative Online Inquiry
KO27618 TOR1B Knockout cell line (HEK293) Human TOR1B 1:3~1:6 Negative Online Inquiry
KO27619 TOR1B Knockout cell line (A549) Human TOR1B 1:3~1:4 Negative Online Inquiry

Background

TOR1B Gene Knockout Cell Lines are genetically engineered cell lines that have had the TOR1B gene functionally disrupted through targeted gene knockout technology. This modification leads to the investigation of the physiological roles of the TOR1B protein, which is implicated in various cellular processes, including neurotransmitter release, synaptic plasticity, and cellular signaling. By utilizing these knockout lines, researchers can explore the downstream effects of TOR1B deficiency, facilitating a better understanding of its contribution to neurodegenerative diseases and other neurological disorders.

These cell lines operate through precise CRISPR-Cas9 gene-editing technology, which ensures high specificity and efficiency in targeting the TOR1B gene. By eliminating TOR1B expression, researchers can assess changes in cellular behavior and protein interaction networks, thus creating a model to study the functional dynamics involved in cellular signaling and network communication. This capability is particularly valuable in elucidating the pathophysiological mechanisms underpinning conditions like dystonia and other movement disorders.

The scientific importance of TOR1B Gene Knockout Cell Lines extends to their applications in both research and clinical settings. They serve as a robust tool for pharmacological studies, enabling the identification of potential therapeutic targets and the screening of small molecules that can modulate signaling pathways affected by TOR1B loss. Unlike alternative methods, such as transient transfection or RNA interference, the knockout approach offers stable phenotypic effects, allowing for long-term studies and reproducibility in experimental results.

Value to researchers and clinicians lies in the ability to generate precise, controlled settings that mimic pathological conditions. The insights gained can lead to significant advancements in treatment frameworks and drug development strategies. Ultimately, these cell lines not only enhance the understanding of TOR1B-related pathways but also foster innovation in therapeutic interventions that could address complex neurological conditions.

Backed by years of expertise in genetic engineering and a commitment to advancing biological research, our company is a trusted provider of high-quality cell lines tailored to meet the diverse needs of the scientific community. Our commitment to rigorous development and quality assurance ensures that researchers can confidently utilize our TOR1B Gene Knockout Cell Lines to drive their discoveries forward.

Please note that all services are for research use only. Not intended for any clinical use.

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