Gene: ANK1
Official Full Name: ankyrin 1provided by HGNC
Gene Summary: Ankyrins are a family of proteins that link the integral membrane proteins to the underlying spectrin-actin cytoskeleton and play key roles in activities such as cell motility, activation, proliferation, contact and the maintenance of specialized membrane domains. Multiple isoforms of ankyrin with different affinities for various target proteins are expressed in a tissue-specific, developmentally regulated manner. Most ankyrins are typically composed of three structural domains: an amino-terminal domain containing multiple ankyrin repeats; a central region with a highly conserved spectrin binding domain; and a carboxy-terminal regulatory domain which is the least conserved and subject to variation. Ankyrin 1, the prototype of this family, was first discovered in the erythrocytes, but since has also been found in brain and muscles. Mutations in erythrocytic ankyrin 1 have been associated in approximately half of all patients with hereditary spherocytosis. Complex patterns of alternative splicing in the regulatory domain, giving rise to different isoforms of ankyrin 1 have been described. Truncated muscle-specific isoforms of ankyrin 1 resulting from usage of an alternate promoter have also been identified. [provided by RefSeq, Dec 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO01602 | ANK1 Knockout cell line (HeLa) | Human | ANK1 | 1:3~1:6 | Negative | Online Inquiry |
KO01603 | ANK1 Knockout cell line (A549) | Human | ANK1 | 1:3~1:4 | Negative | Online Inquiry |
ANK1 Gene Knockout Cell Lines are genetically engineered cellular models that have undergone a selective disruption of the ANK1 gene, which encodes for ankyrin 1—a crucial cytoskeletal protein involved in maintaining cell membrane integrity and regulating the architecture of the cell. By employing techniques such as CRISPR/Cas9 gene editing, these cell lines effectively eliminate the expression of ANK1, allowing researchers to investigate the gene’s functional roles in various biological processes.
The key function of the ANK1 Gene Knockout Cell Lines lies in their ability to provide insight into the physiological and pathological implications of ankyrin 1 deficiency. By creating a controlled environment where the gene is absent, researchers can observe alterations in cell morphology, signaling pathways, and interactions with other cellular components. This is invaluable in dissecting the gene’s contributions to diseases such as hereditary spherocytosis and other erythrocyte disorders, where abnormal red blood cell shape and function are often seen.
The scientific importance of using ANK1 Gene Knockout Cell Lines extends to both research and clinical applications. These models serve as powerful tools for drug discovery, enabling the screening of therapeutic compounds that target pathways affected by ANK1 manipulation. They also aid in understanding genetic contributions to conditions influenced by cellular biomechanics, thereby informing potential gene therapies.
Compared to alternative models, the ANK1 Gene Knockout Cell Lines stand out due to their precise genetic modification and the ability to replicate human cellular responses. This specificity not only enhances the relevancy of experimental outcomes but also reduces the likelihood of off-target effects that can arise with less precise genetic manipulation techniques.
Researchers and clinicians benefit significantly from the use of these cell lines, as they provide a robust framework for advancing knowledge in cell biology, disease mechanisms, and therapeutic development. These models are particularly valuable in fostering collaborations between academic and clinical environments, enabling translational research that can bring discoveries from the bench to the bedside.
[Your Company] has a proven track record in delivering high-quality biological products and cutting-edge research tools. Our expertise ensures that the ANK1 Gene Knockout Cell Lines undergo rigorous quality control measures, making them an essential addition to your research toolkit and contributing to your scientific success.
Please note that all services are for research use only. Not intended for any clinical use.
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