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NSD2 Knockout Cell Lines

Gene: NSD2

Official Full Name: nuclear receptor binding SET domain protein 2provided by HGNC

Gene Summary: This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO03324 NSD2 Knockout cell line (HeLa) Human NSD2 1:3~1:6 Negative Online Inquiry
KO03325 NSD2 Knockout cell line (HCT 116) Human NSD2 1:2~1:4 Negative Online Inquiry
KO03326 NSD2 Knockout cell line (HEK293) Human NSD2 1:3~1:6 Negative Online Inquiry
KO03327 NSD2 Knockout cell line (A549) Human NSD2 1:3~1:4 Negative Online Inquiry

Background

NSD2 Gene Knockout Cell Lines are genetically engineered cellular models designed to eliminate the expression of the NSD2 gene, which encodes a histone methyltransferase involved in chromatin remodeling and gene regulation. These cell lines serve as powerful tools for studying the functional implications of NSD2 loss in various biological processes, including cell proliferation, differentiation, and responses to external stimuli. By employing CRISPR-Cas9 technology for precise gene editing, these knockout cell lines provide researchers with a reliable system for dissecting the role of NSD2 in oncogenesis, epigenetic regulation, and disease pathology.

The primary mechanism through which NSD2 Gene Knockout Cell Lines operate involves the disruption of NSD2's enzymatic activity, leading to alterations in histone methylation patterns and subsequent changes in gene expression profiles. This disruption allows researchers to investigate the downstream effects on cellular behavior and signaling pathways, providing insights into the implications of NSD2 dysregulation in cancer and developmental disorders. Their use in functional genomics and pharmacological studies has proven essential in elucidating the complex regulatory mechanisms governed by histone modifications.

The scientific importance of NSD2 Gene Knockout Cell Lines extends into both research and clinical settings, as they offer a robust platform for drug discovery and validation. They enable the investigation of novel therapeutics targeting epigenetic modifications, thus contributing to the development of tailored therapeutic strategies in cancer treatment and other NSD2-associated conditions.

Compared to traditional knockdown methodologies, such as siRNA or shRNA approaches, NSD2 Gene Knockout Cell Lines provide a more stable and permanent modification of the target gene, leading to consistent experimental outcomes. This permanence offers significant advantages for long-term studies and enables comprehensive analyses of gene function and regulation.

For researchers and clinicians focused on exploring the facets of gene regulation and cancer biology, NSD2 Gene Knockout Cell Lines represent an invaluable resource. Their precise gene editing capabilities facilitate significant advancements in the understanding of gene function, thus paving the way for innovation in therapeutic approaches.

With a strong commitment to precision and quality, our company specializes in developing advanced biological research tools that empower the scientific community to drive breakthroughs in genomics and disease research.

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

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