Gene: SYNE1
Official Full Name: spectrin repeat containing nuclear envelope protein 1provided by HGNC
Gene Summary: This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO03169 | SYNE1 Knockout cell line (HeLa) | Human | SYNE1 | 1:3~1:6 | Negative | Online Inquiry |
KO03170 | SYNE1 Knockout cell line (HCT 116) | Human | SYNE1 | 1:2~1:4 | Negative | Online Inquiry |
KO03171 | SYNE1 Knockout cell line (HEK293) | Human | SYNE1 | 1:3~1:6 | Negative | Online Inquiry |
KO03172 | SYNE1 Knockout cell line (A549) | Human | SYNE1 | 1:3~1:4 | Negative | Online Inquiry |
SYNE1 Gene Knockout Cell Lines are specialized cellular models designed to investigate the biological functions of the SYNE1 gene, which plays a crucial role in maintaining cellular architecture and nuclear positioning. By employing advanced gene-editing techniques such as CRISPR-Cas9, these cell lines effectively disrupt the expression of SYNE1, enabling researchers to study downstream effects related to cell signaling, migration, and mechanotransduction.
The primary function of these knockout cell lines is to provide a controlled environment for evaluating the consequences of SYNE1 loss on cellular behavior and physiology. Mechanistically, the absence of SYNE1 alters the interaction between the cytoskeleton and the nuclear envelope, leading to changes in cellular morphology and functional cell organization. This disruption can serve as a valuable model for examining diseases linked to nuclear positioning defects, such as muscular dystrophies and certain neurological disorders.
The scientific importance of SYNE1 Gene Knockout Cell Lines is underscored by their applications in both fundamental research and clinical settings. They have proven instrumental in elucidating the molecular pathways affected by SYNE1 deficiencies, which can provide insights into therapeutic targets for diseases characterized by cytoskeletal abnormalities. Furthermore, these cell lines facilitate high-throughput screening processes, allowing for the identification of potential drug compounds that may alleviate the symptoms associated with SYNE1-related disorders.
Compared to traditional cell lines that may not accurately reflect genetic modifications, SYNE1 Gene Knockout Cell Lines provide a distinct advantage by allowing researchers to work with a biologically relevant model that mirrors the consequences of gene loss. This specificity enhances the reliability of experimental outcomes, solidifying their position as a preferred choice for genetic studies.
For researchers and clinicians, the value of SYNE1 Gene Knockout Cell Lines lies in their capacity to drive innovative research and contribute to the understanding of genetic and degenerative diseases. They empower users to advance their studies with precision and confidence in their models.
Our company prides itself on offering cutting-edge biological tools and resources, backed by extensive expertise in gene editing and cell line development. We are committed to supporting the scientific community in advancing research and improving patient outcomes through our high-quality products.
Please note that all services are for research use only. Not intended for any clinical use.
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