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NSD1 Knockout Cell Lines

Gene: NSD1

Official Full Name: nuclear receptor binding SET domain protein 1provided by HGNC

Gene Summary: This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Sep 2018]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03392 NSD1 Knockout cell line (HeLa) Human NSD1 1:3~1:6 Negative Online Inquiry
KO03393 NSD1 Knockout cell line (HCT 116) Human NSD1 1:2~1:4 Negative Online Inquiry
KO03394 NSD1 Knockout cell line (HEK293) Human NSD1 1:3~1:6 Negative Online Inquiry
KO03395 NSD1 Knockout cell line (A549) Human NSD1 1:3~1:4 Negative Online Inquiry

Background

NSD1 Gene Knockout Cell Lines are specialized cellular models engineered through advanced genome editing techniques to lack the functional expression of the NSD1 gene. NSD1 (nuclear receptor-binding SET domain protein 1) is implicated in various critical cellular processes, including transcription regulation, chromatin remodeling, and cell cycle control. By creating a knockout of this gene, researchers can delve into its role in cellular functions and study the associated consequences of its absence.

The core mechanism of these cell lines involves CRISPR-Cas9 technology, which allows precise modifications at targeted genetic loci. The NSD1 knockout leads to alterations in gene expression profiles, enabling researchers to investigate pathways governed by NSD1 and its involvement in pathological conditions such as developmental disorders and certain cancers. The availability of these cell lines opens avenues for functional assays, drug screening, and the exploration of NSD1's role in epigenetic regulation.

The scientific importance of NSD1 Gene Knockout Cell Lines cannot be overstated, as they provide a vital tool in the understanding of epigenetic modifications and their impact on human health. Researchers in academic and clinical settings can employ these models to develop targeted therapies that address NSD1-mediated malignancies or genetic disorders.

Compared to alternative models, such as wild-type cell lines or other knockout systems, NSD1 Gene Knockout Cell Lines offer distinct advantages, including high specificity and relevancy in studies focused on malignancies linked to epigenetic changes. Their distinct genetic background allows for more precise interpretations of experimental results, ultimately leading to more successful translations into potential therapeutic strategies.

Researchers, clinicians, and pharmaceutical developers will find these cell lines invaluable for their capacity to reveal new biological insights and therapeutic approaches. With a commitment to providing cutting-edge biological products, our company leverages extensive expertise in gene editing technologies, ensuring that our clients have access to the highest-quality research tools to advance their scientific endeavors.

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

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