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LMNA Knockout Cell Lines

Gene: LMNA

Official Full Name: lamin A/Cprovided by HGNC

Gene Summary: The protein encoded by this gene is part of the nuclear lamina, a two-dimensional matrix of proteins located next to the inner nuclear membrane. The lamin family of proteins make up the matrix and are highly conserved in evolution. During mitosis, the lamina matrix is reversibly disassembled as the lamin proteins are phosphorylated. Lamin proteins are thought to be involved in nuclear stability, chromatin structure and gene expression. Vertebrate lamins consist of two types, A and B. Alternative splicing results in multiple transcript variants. Mutations in this gene lead to several diseases: Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome. [provided by RefSeq, May 2022]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO07161 LMNA Knockout cell line (HeLa) Human LMNA 1:3~1:6 Negative Online Inquiry
KO07162 LMNA Knockout cell line (HCT 116) Human LMNA 1:2~1:4 Negative Online Inquiry
KO07163 LMNA Knockout cell line (HEK293) Human LMNA 1:3~1:6 Negative Online Inquiry
KO07164 LMNA Knockout cell line (A549) Human LMNA 1:3~1:4 Negative Online Inquiry

Background

LMNA Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to lack the expression of the LMNA gene, which encodes for lamin A/C, vital components of the nuclear lamina. These cell lines serve as invaluable tools for studying the functional roles of lamin proteins in cellular structure and dynamics, nuclear stability, and gene expression regulation. By providing a model system that mimics specific pathological states, researchers can elucidate the implications of LMNA mutations linked to various diseases, including muscular dystrophies, cardiomyopathies, and progeria syndromes.

The key function of LMNA Gene Knockout Cell Lines lies in their ability to enable scientists to investigate the consequences of lamin A/C deficiency on cellular processes. The absence of the LMNA gene allows researchers to dissect signaling pathways and structural changes that accompany nuclear envelope instability and altered cellular function. These cell lines facilitate the exploration of drug candidates, thereby advancing therapeutic strategies aimed at ameliorating the effects of LMNA-related disorders.

Scientific importance extends beyond basic research; in clinical settings, these cell lines can be instrumental in developing gene therapies and personalized medicine approaches. Their unique advantages include the ability to study disease mechanisms in a controlled environment, reproducibility of results, and the capacity to customize for specific experimental conditions compared to other non-targeted models.

For researchers and clinicians, LMNA Gene Knockout Cell Lines represent a significant advancement in experimental biology, enabling deeper insights into cellular pathology and therapeutic development. Their established use in prominent laboratories assures users of their quality and relevance to ongoing research initiatives.

With extensive expertise in genetic engineering and cell biology, our company is dedicated to providing high-quality biological products that empower scientific discovery and innovation.

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

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