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ZNF513 Knockout Cell Lines

Gene: ZNF513

Official Full Name: zinc finger protein 513provided by HGNC

Gene Summary: The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO26614 ZNF513 Knockout cell line (HeLa) Human ZNF513 1:3~1:6 Negative Online Inquiry
KO26615 ZNF513 Knockout cell line (HCT 116) Human ZNF513 1:2~1:4 Negative Online Inquiry
KO26616 ZNF513 Knockout cell line (HEK293) Human ZNF513 1:3~1:6 Negative Online Inquiry
KO26617 ZNF513 Knockout cell line (A549) Human ZNF513 1:3~1:4 Negative Online Inquiry

Background

ZNF513 Gene Knockout Cell Lines are specialized cellular models generated through targeted gene editing techniques aimed at knocking out the ZNF513 gene. This gene is part of the zinc finger protein family, which plays critical roles in various cellular processes including transcriptional regulation, DNA repair, and apoptosis. By creating knockout cell lines, researchers can elucidate the functional significance of ZNF513, enabling in-depth studies on its involvement in cellular responses, disease pathways, and potential therapeutic targets.

The mechanism behind these cell lines involves the utilization of CRISPR-Cas9 technology, which allows for precise editing of the genome. By designing specific guide RNAs that target the ZNF513 locus, the Cas9 nuclease induces double-strand breaks, leading to insertions or deletions that results in gene inactivation. This method not only ensures a high efficiency of knockout but also a stable genetic modification, permitting continuous observation of cellular behavior over time.

Scientifically, ZNF513 knockout cell lines are significant in various fields such as cancer research, where the role of transcription factors in tumorigenesis is investigated, as well as in studies of somatic cell reprogramming and stem cell biology. In clinical settings, insights gained from these models could translate into novel therapeutic strategies, as understanding the full ramifications of ZNF513 loss may reveal potential biomarkers or targets for intervention.

Comparing ZNF513 knockout cell lines to alternative models, they offer enhanced specificity and reliability. Traditional methods such as RNA interference may lead to off-target effects or incomplete gene silencing. In contrast, knockout cell lines derived from CRISPR technology ensure a complete loss of function and a more accurate representation of the biological consequences.

For researchers and clinicians alike, the ability to study the ZNF513 gene within a controlled environment presents immense value. With these knockout cell lines, users gain a powerful tool for dissecting gene functions and validating research findings.

Our company is committed to advancing biological research by providing high-quality, innovative cell line products developed through state-of-the-art methodologies and expertise in molecular biology. Through our offerings, researchers can achieve profound insights and drive forward the boundaries of scientific discovery.

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

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