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TUBA1A Knockout Cell Lines

Gene: TUBA1A

Official Full Name: tubulin alpha 1aprovided by HGNC

Gene Summary: Microtubules of the eukaryotic cytoskeleton perform essential and diverse functions and are composed of a heterodimer of alpha and beta tubulins. The genes encoding these microtubule constituents belong to the tubulin superfamily, which is composed of six distinct families. Genes from the alpha, beta and gamma tubulin families are found in all eukaryotes. The alpha and beta tubulins represent the major components of microtubules, while gamma tubulin plays a critical role in the nucleation of microtubule assembly. There are multiple alpha and beta tubulin genes, which are highly conserved among species. This gene encodes alpha tubulin and is highly similar to the mouse and rat Tuba1 genes. Northern blot studies have shown that the gene expression is predominantly found in morphologically differentiated neurologic cells. This gene is one of three alpha-tubulin genes in a cluster on chromosome 12q. Mutations in this gene cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly, intellectual disability, and early-onset epilepsy caused by defective neuronal migration. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO34421 TUBA1A Knockout cell line (HeLa) Human TUBA1A 1:3~1:6 Negative Online Inquiry
KO34422 TUBA1A Knockout cell line (HCT 116) Human TUBA1A 1:2~1:4 Negative Online Inquiry
KO34423 TUBA1A Knockout cell line (HEK293) Human TUBA1A 1:3~1:6 Negative Online Inquiry
KO34424 TUBA1A Knockout cell line (A549) Human TUBA1A 1:3~1:4 Negative Online Inquiry

Background

TUBA1A Gene Knockout Cell Lines represent a groundbreaking approach to studying the roles of the TUBA1A gene, which encodes the alpha-tubulin protein essential for microtubule dynamics and cytoskeletal organization. These cell lines are engineered using CRISPR-Cas9 technology to effectively disrupt the TUBA1A gene, leading to a loss of function in the encoded protein. This knockout model provides researchers with a powerful tool to investigate the biological consequences of TUBA1A deficiency, revealing insights into cellular processes such as mitosis, intracellular transport, and neuronal development.

The primary mechanism by which these cell lines operate involves the precise deletion of the TUBA1A gene, which significantly alters microtubule stability and functionality. By studying the resultant phenotypic changes, researchers can dissect the pathways linked to diseases where microtubule dysregulation plays a crucial role, such as neurodegenerative disorders and cancer. In clinical settings, these knockout cell lines offer a platform for potential therapeutic drug testing, allowing for the screening of compounds that may restore microtubule function or mitigate the effects of TUBA1A loss.

Compared to traditional methods like RNA interference, TUBA1A Gene Knockout Cell Lines provide more reliable and permanent modifications of gene expression, ensuring reproducibility in experimental outcomes. Additionally, the specificity of CRISPR-Cas9 enables targeted gene manipulation, minimizing off-target effects that can complicate data interpretation.

For researchers and clinicians alike, the value of TUBA1A Gene Knockout Cell Lines is immense, as they facilitate a deeper understanding of cellular mechanisms and foster the development of innovative treatments. Our commitment to advancing biological research is underscored by our expertise in creating high-quality, customizable cell lines, ensuring that our products meet the diverse needs of the scientific community.

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

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