Gene: TMEM67
Official Full Name: transmembrane protein 67provided by HGNC
Gene Summary: The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO23529 | TMEM67 Knockout cell line (HeLa) | Human | TMEM67 | 1:3~1:6 | Negative | Online Inquiry |
KO23530 | TMEM67 Knockout cell line (HCT 116) | Human | TMEM67 | 1:2~1:4 | Negative | Online Inquiry |
KO23531 | TMEM67 Knockout cell line (HEK293) | Human | TMEM67 | 1:3~1:6 | Negative | Online Inquiry |
KO23532 | TMEM67 Knockout cell line (A549) | Human | TMEM67 | 1:3~1:4 | Negative | Online Inquiry |
TMEM67 Gene Knockout Cell Lines are specialized cellular models engineered to lack the TMEM67 gene, a critical player in the pathway associated with ciliogenesis and signal transduction within the primary cilium. These knockout cell lines serve as essential tools for understanding the genetic and molecular mechanisms underlying various cellular processes, particularly those related to the cilia’s role in homeostasis and cellular signaling. By systematically removing the TMEM67 gene, researchers can effectively mimic disease states associated with ciliary dysfunction, such as polycystic kidney disease and Joubert syndrome.
The primary function of TMEM67 Gene Knockout Cell Lines is to provide a platform for studying the downstream effects of TMEM67 depletion. The absence of the gene alters cellular behavior, including changes in morphogenesis, proliferation, and signaling pathways mediated by the cilia. This provides invaluable insights into the complex interactions between cilia and cellular functions, facilitating research into therapeutic targets for ciliary-related diseases.
The scientific importance of these cell lines extends to both basic and translational research. In preclinical studies, they aid in assessing the efficacy and mechanism of action of potential drug candidates aiming to treat ciliary disorders. Similarly, their unique ability to provide a controlled in vitro environment accelerates discoveries in gene therapy and regenerative medicine.
Compared to other models, TMEM67 Gene Knockout Cell Lines offer distinct advantages, including the ability to closely replicate the pathogenic phenotype observed in human disorders related to TMEM67 deficiency. This makes them a valuable alternative to traditional models that may not adequately reflect the biological complexity or heterogeneity of human conditions.
For researchers and clinicians, the TMEM67 Gene Knockout Cell Lines represent a strategic investment in the study of ciliary biology and associated diseases, helping to fill critical knowledge gaps and drive innovations in clinical care. Our company specializes in developing high-quality, precision-engineered cell lines that empower the scientific community to uncover key biological truths and advance therapeutic strategies.
Please note that all services are for research use only. Not intended for any clinical use.
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