Gene: ARNT2
Official Full Name: aryl hydrocarbon receptor nuclear translocator 2provided by HGNC
Gene Summary: This gene encodes a member of the basic-helix-loop-helix-Per-Arnt-Sim (bHLH-PAS) superfamily of transcription factors. The encoded protein acts as a partner for several sensor proteins of the bHLH-PAS family, forming heterodimers with the sensor proteins that bind regulatory DNA sequences in genes responsive to developmental and environmental stimuli. Under hypoxic conditions, the encoded protein complexes with hypoxia-inducible factor 1alpha in the nucleus and this complex binds to hypoxia-responsive elements in enhancers and promoters of oxygen-responsive genes. A highly similar protein in mouse forms functional complexes with both aryl hydrocarbon receptors and Single-minded proteins, suggesting additional roles for the encoded protein in the metabolism of xenobiotic compounds and the regulation of neurogenesis, respectively. [provided by RefSeq, Dec 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO32519 | ARNT2 Knockout cell line (HCT 116) | Human | ARNT2 | 1:2~1:4 | Negative | Online Inquiry |
KO32520 | ARNT2 Knockout cell line (HEK293) | Human | ARNT2 | 1:3~1:6 | Negative | Online Inquiry |
KO32521 | ARNT2 Knockout cell line (A549) | Human | ARNT2 | 1:3~1:4 | Negative | Online Inquiry |
ARNT2 Gene Knockout Cell Lines are specifically engineered cell lines that have been utilized to create a functional deficiency of the ARNT2 (Aryl Hydrocarbon Receptor Nuclear Translocator 2) gene. This knockout functionality enables researchers to investigate the biological roles of ARNT2 in various cellular processes, including cell signaling, differentiation, and response to environmental cues. By eliminating the expression of this gene, these cell lines provide a controlled environment to study the downstream effects and pathways influenced by ARNT2 activity.
The primary mechanism by which ARNT2 Gene Knockout Cell Lines operate involves the loss of ARNT2 protein, a key component of heterodimer complexes with other transcription factors like the Aryl Hydrocarbon Receptor (AhR). This is particularly significant in cellular contexts where ARNT2 has been implicated in mediating responses to hypoxia, inflammatory processes, and the development of certain cancers. By utilizing these knockout lines, researchers can dissect the molecular consequences of ARNT2 deficiency, unraveling its role in gene regulation and contributing to a deeper understanding of disease mechanisms.
In the context of scientific research and clinical applications, ARNT2 Gene Knockout Cell Lines hold paramount importance. They facilitate the exploration of ARNT2's role in various pathologies, particularly its involvement in tumor biology and metabolic disorders. Moreover, they serve as a valuable tool in drug discovery, allowing for the identification of novel therapeutic targets and biomarkers.
What sets ARNT2 Gene Knockout Cell Lines apart from conventional cell lines is their precision engineering and reliability in providing replicable, consistent results. Unlike other models that may exhibit variable expression of target genes, these knockout lines deliver a definitive absence of ARNT2 function, significantly enhancing the quality of experimental outcomes. Additionally, their application across a range of cellular contexts broadens their utility, making them suitable for various types of studies—from basic biology to translational research.
Ultimately, ARNT2 Gene Knockout Cell Lines represent a critical resource for researchers and clinicians seeking to elucidate the complexities surrounding ARNT2's biological functions and its implications in health and disease. By choosing our ARNT2 Gene Knockout Cell Lines, you gain access to meticulously developed tools backed by our commitment to quality and innovation in biological products, empowering you to advance your research objectives effectively.
Please note that all services are for research use only. Not intended for any clinical use.
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