Gene: ARL13B
Official Full Name: ARF like GTPase 13Bprovided by HGNC
Gene Summary: This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03535 | ARL13B Knockout cell line (HeLa) | Human | ARL13B | 1:3~1:6 | Negative | Online Inquiry |
KO03536 | ARL13B Knockout cell line (HCT 116) | Human | ARL13B | 1:2~1:4 | Negative | Online Inquiry |
KO03537 | ARL13B Knockout cell line (HEK293) | Human | ARL13B | 1:3~1:6 | Negative | Online Inquiry |
KO03538 | ARL13B Knockout cell line (A549) | Human | ARL13B | 1:3~1:4 | Negative | Online Inquiry |
ARL13B Gene Knockout Cell Lines are specialized cell lines that have undergone targeted genome editing to disrupt the ARL13B gene, which plays a critical role in cilia formation and function. This innovative biological product allows researchers to study the effects of ARL13B depletion on cellular processes and signaling pathways, thereby elucidating its involvement in various physiological and pathological conditions, including cancers and ciliopathies.
The primary function of ARL13B Gene Knockout Cell Lines lies in their ability to mimic physiological conditions where ARL13B is absent. This enables scientists to explore the molecular mechanisms by which this gene influences cell behavior, morphology, and intercellular communication. Mechanistically, ARL13B is associated with the regulation of cilium structure and intracellular signaling; its disruption renders cells incapable of maintaining normal ciliary function, marking an essential area of study for understanding diseases linked to ciliary dysfunction.
The scientific importance of these cell lines is underscored by their applicability in both fundamental research and therapeutic discovery. They serve as invaluable tools for drug screening, target validation, and functional genomics, facilitating a deeper understanding of gene function in health and disease. The use of ARL13B knockout models can be particularly pivotal in studying neurodevelopmental disorders, where ciliary defects are implicated.
Compared to alternative models, such as overexpressing or silencing genes in wild-type cells, ARL13B Gene Knockout Cell Lines provide a more accurate representation of the gene's loss-of-function effects. This specificity not only enhances experimental reproducibility but also yields insights into pathophysiological mechanisms that are often obscured in non-knockout models.
For researchers and clinicians aiming to innovate in genetic research and therapeutic strategies, ARL13B Gene Knockout Cell Lines present a unique opportunity to uncover new avenues for intervention. Our company prides itself on expertise in producing high-fidelity genome-edited cell lines, backed by rigorous validation processes and extensive characterization. Through our commitment to quality, we empower the scientific community with tools that accelerate discovery and facilitate better health outcomes.
Please note that all services are for research use only. Not intended for any clinical use.
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