Home / ATXN7 Knockout Cell Lines

ATXN7 Knockout Cell Lines

Gene: ATXN7

Official Full Name: ataxin 7provided by HGNC

Gene Summary: The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the 'pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. This locus has been mapped to chromosome 3, and it has been determined that the diseased allele associated with spinocerebellar ataxia-7 contains 37-306 CAG repeats (near the N-terminus), compared to 4-35 in the normal allele. The encoded protein is a component of the SPT3/TAF9/GCN5 acetyltransferase (STAGA) and TBP-free TAF-containing (TFTC) chromatin remodeling complexes, and it thus plays a role in transcriptional regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]

Get A Quote
Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35508 ATXN7 Knockout cell line (HeLa) Human ATXN7 1:3~1:6 Negative Online Inquiry
KO35509 ATXN7 Knockout cell line (HCT 116) Human ATXN7 1:2~1:4 Negative Online Inquiry
KO35510 ATXN7 Knockout cell line (HEK293) Human ATXN7 1:3~1:6 Negative Online Inquiry
KO35511 ATXN7 Knockout cell line (A549) Human ATXN7 1:3~1:4 Negative Online Inquiry

Background

ATXN7 Gene Knockout Cell Lines are specialized cellular models engineered to lack the expression of the ATXN7 gene, which encodes ataxin-7, a protein implicated in neurodegenerative disorders such as Spinocerebellar Ataxia Type 7 (SCA7). These knockout cell lines serve as critical tools for studying gene function, elucidating disease mechanisms, and screening potential therapeutic agents. By depleting ATXN7, researchers can investigate the biochemical and physiological consequences of its absence, providing insight into the cellular pathways affected in SCA7 and related conditions.

The key mechanism through which these cell lines operate hinges on the CRISPR-Cas9 gene-editing technology, which precisely targets and deactivates the ATXN7 gene. This specificity allows researchers to observe the resultant phenotypic changes, such as altered protein interactions and cellular distress responses, which can lead to a deeper understanding of ataxin-7's role in neuronal health and pathology. Furthermore, these models facilitate drug discovery efforts by enabling high-throughput screening of compounds that may inhibit or reverse the effects of ATXN7 loss.

From a scientific perspective, the ATXN7 Gene Knockout Cell Lines are invaluable in both research and clinical settings. They not only contribute to the fundamental understanding of SCA7 but also enable the exploration of gene therapy options and regenerative medicine approaches. Compared to conventional cell lines, these knockout models offer precise genetic manipulation, allowing for more reliable and reproducible outcomes in experimental assays.

One of the distinct advantages of our ATXN7 Gene Knockout Cell Lines is the robustness and reliability of the knockout, validated through genomic sequencing and functional assays. This quality assurance ensures that researchers can trust the data generated from these lines, making them a superior choice over non-targeted cell lines or less specific knockdown methods.

In conclusion, our ATXN7 Gene Knockout Cell Lines are essential for researchers and clinicians focused on neurodegenerative diseases, providing a unique and advanced platform for discovery and innovation. As a pioneer in biological product offerings, our company is committed to delivering cutting-edge tools that empower scientific advancements, assisting the research community in tackling the challenges of genetic disorders.

Please note that all services are for research use only. Not intended for any clinical use.

Get a free quote

If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.

0

There is no product in your cart.