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PNKD Knockout Cell Lines

Gene: PNKD

Official Full Name: PNKD metallo-beta-lactamase domain containingprovided by HGNC

Gene Summary: This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO02587 PNKD Knockout cell line (HeLa) Human PNKD 1:3~1:6 Negative Online Inquiry
KO02588 PNKD Knockout cell line (HCT 116) Human PNKD 1:2~1:4 Negative Online Inquiry
KO02589 PNKD Knockout cell line (HEK293) Human PNKD 1:3~1:6 Negative Online Inquiry
KO02590 PNKD Knockout cell line (A549) Human PNKD 1:3~1:4 Negative Online Inquiry

Background

PNKD Gene Knockout Cell Lines are engineered cellular models that harbor targeted gene deletions of the PNKD gene, which has been implicated in various neurological disorders such as dystonia and paroxysmal kinesigenic dyskinesia. These cell lines are created using advanced techniques such as CRISPR/Cas9 gene editing, enabling precise modifications to the genome that allow researchers to investigate the functional consequences of PNKD loss of function. By utilizing these knockout models, scientists can delve into the molecular pathways and cellular mechanisms affected by PNKD depletion, enabling a deeper understanding of its role in neurophysiology.

The key functions of PNKD Gene Knockout Cell Lines are to serve as platforms for studying the cellular response to the absence of the PNKD gene and to facilitate the development of targeted therapeutic strategies. By observing how these cell lines behave in comparison to their wild-type counterparts, researchers can assess changes in cellular signaling, gene expression profiles, and phenotype alterations attributable to PNKD inactivation. This mechanistic insight is crucial for identifying potential drug targets and validating therapeutic modalities aimed at addressing PNKD-linked conditions.

Scientifically, the PNKD Gene Knockout Cell Lines have substantial importance in both research and clinical contexts. They provide a crucial tool for neuroscience research, allowing for the exploration of PNKD's involvement in neurotransmitter release, synaptic plasticity, and neuromodulatory processes. These insights can contribute to the development of novel treatment strategies for patients suffering from movement disorders.

In comparison to traditional methods of studying gene function, such as employing pharmacological inhibition or transgenic models that require significant time investment, the PNKD Gene Knockout Cell Lines are advantageous due to their rapid implementation and high throughput capability. They enable researchers to generate reproducible data efficiently, streamlining the process of hypothesis testing and experimental validation.

For researchers and clinicians keen on advancing their understanding and treatment of neurological conditions, the PNKD Gene Knockout Cell Lines represent a valuable asset. They facilitate investigations that can significantly impact therapeutic development and patient care. Our company specializes in providing high-quality biological products and tools tailored to support pioneering research initiatives, underpinned by our commitment to scientific excellence and innovation. Through rigorous production standards and a deep understanding of molecular genetics, we deliver products that empower the scientific community to explore and elucidate complex biological systems.

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

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