Gene: RHOT2
Official Full Name: ras homolog family member T2provided by HGNC
Gene Summary: This gene encodes a member of the Rho family of GTPases. The encoded protein is localized to the outer mitochondrial membrane and plays a role in mitochondrial trafficking and fusion-fission dynamics. [provided by RefSeq, Nov 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03630 | RHOT2 Knockout cell line (HeLa) | Human | RHOT2 | 1:3~1:6 | Negative | Online Inquiry |
KO03631 | RHOT2 Knockout cell line (HCT 116) | Human | RHOT2 | 1:2~1:4 | Negative | Online Inquiry |
KO03632 | RHOT2 Knockout cell line (HEK293) | Human | RHOT2 | 1:3~1:6 | Negative | Online Inquiry |
KO03633 | RHOT2 Knockout cell line (A549) | Human | RHOT2 | 1:3~1:4 | Negative | Online Inquiry |
RHOT2 Gene Knockout Cell Lines are advanced genomic tools that facilitate the study of mitochondrial dynamics and cellular signaling by enabling researchers to investigate the functional role of the RHOT2 gene. RHOT2 (Ras Homolog Family Member T2) is critically involved in mitochondrial transport, influencing cellular energy production and apoptosis pathways. By employing CRISPR/Cas9 gene-editing technology, these knockout cell lines effectively disrupt the RHOT2 gene, allowing for a deeper understanding of its role in cellular physiology.
The primary function of the RHOT2 knockout cell lines lies in their ability to mimic specific pathological conditions associated with mitochondrial dysfunction. Researchers utilize these models to elucidate the mechanistic underpinnings of diseases such as neurodegenerative disorders, cancer, and metabolic syndromes, where mitochondrial activity is often compromised. The knockout models allow for the assessment of mitochondrial morphology, cellular respiration, and the investigation of signaling pathways that are modulated by RHOT2.
Scientifically, the RHOT2 knockout cell lines represent a significant advancement over traditional methods such as RNA interference, as they provide full gene disruption, enabling more precise investigations into gene function. This precision offers researchers an opportunity to generate reproducible results that can validate their hypotheses with a high degree of confidence. Furthermore, the use of knockout models assists in drug discovery and therapeutic development, as they enable the screening of compounds that may correct or mitigate the phenotypic effects of loss of RHOT2 functionality.
What distinguishes our RHOT2 Gene Knockout Cell Lines from alternatives is the rigorous quality control and characterization established during their development. Each line undergoes extensive validation to confirm the absence of RHOT2 expression, ensuring that users receive a reliable tool for their research. Our commitment to providing customizable cell lines tailored to specific research needs enhances the versatility and utility of these models.
For researchers and clinicians alike, the RHOT2 Gene Knockout Cell Lines offer an invaluable resource in the quest to decipher complex cellular mechanisms and improve therapeutic strategies. The insights garnered from these cell lines have the potential to pave the way for innovative treatments targeting mitochondrial-related disorders.
At our company, we bring years of expertise in cellular biology and innovative genetic engineering techniques, ensuring that our products not only meet but exceed the expectations of the scientific community, empowering breakthroughs in biomedical research.
Please note that all services are for research use only. Not intended for any clinical use.
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