Gene: BRD2
Official Full Name: bromodomain containing 2provided by HGNC
Gene Summary: This gene encodes a transcriptional regulator that belongs to the BET (bromodomains and extra terminal domain) family of proteins. This protein associates with transcription complexes and with acetylated chromatin during mitosis, and it selectively binds to the acetylated lysine-12 residue of histone H4 via its two bromodomains. The gene maps to the major histocompatability complex (MHC) class II region on chromosome 6p21.3, but sequence comparison suggests that the protein is not involved in the immune response. This gene has been implicated in juvenile myoclonic epilepsy, a common form of epilepsy that becomes apparent in adolescence. Multiple alternatively spliced variants have been described for this gene. [provided by RefSeq, Dec 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO02956 | BRD2 Knockout cell line (HeLa) | Human | BRD2 | 1:3~1:6 | Negative | Online Inquiry |
KO02957 | BRD2 Knockout cell line (HCT 116) | Human | BRD2 | 1:2~1:4 | Negative | Online Inquiry |
KO02958 | BRD2 Knockout cell line (HEK293) | Human | BRD2 | 1:3~1:6 | Negative | Online Inquiry |
KO02959 | BRD2 Knockout cell line (A549) | Human | BRD2 | 1:3~1:4 | Negative | Online Inquiry |
BRD2 Gene Knockout Cell Lines are genetically modified cell lines in which the BRD2 gene has been inactivated or “knocked out.” The BRD2 gene encodes a member of the bromodomain and extraterminal (BET) protein family, which plays a pivotal role in regulating gene expression by interacting with acetylated lysines on histones. By utilizing techniques such as CRISPR-Cas9 or homologous recombination, these cell lines facilitate the study of BRD2's biological functions, including its involvement in cell proliferation, differentiation, and transcriptional regulation.
BRD2 knockout cell lines allow researchers to dissect the molecular pathways influenced by BRD2 activity, rendering them invaluable in understanding various diseases, particularly cancer, where aberrant BRD2 expression is often implicated. These models can thus serve as excellent platforms for drug discovery and development, enabling the screening of BRD2-targeting compounds and examining their therapeutic efficacy.
One of the main advantages of our BRD2 Gene Knockout Cell Lines is their reliability and reproducibility. Compared to traditional methods of gene knockdown, such as RNA interference, which can be transient and variable, our knockout lines provide a stable loss-of-function model that precisely reflects the absence of BRD2, making experimental results more robust. Furthermore, these cell lines can be used in combination with other genomic, transcriptomic, and proteomic analyses to provide a comprehensive understanding of cellular responses to therapeutic agents.
For researchers and clinicians, these cell lines significantly streamline the process of investigating BRD2-related mechanisms, ultimately advancing the field of epigenetics and therapeutic design. Our company's dedication to cutting-edge genomic technologies and expertise in gene editing empowers users with high-quality biological products that meet the rigorous demands of modern scientific research. Whether in academic, pharmaceutical, or clinical settings, our BRD2 Gene Knockout Cell Lines are essential tools for pioneering innovative approaches in disease treatment and understanding.
Please note that all services are for research use only. Not intended for any clinical use.
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