Gene: NAT8B
Official Full Name: N-acetyltransferase 8B (putative, gene/pseudogene)provided by HGNC
Gene Summary: This gene is highly similar to the N-acetyltransferase 8 (NAT8) gene which encodes a kidney and liver protein with homology to bacterial acetyltransferases involved in drug resistance. This gene is localized on chromosome 2 in the vicinity of the NAT8 gene and represents a human-specific transcribed pseudogene of NAT8. This gene contains two common polymorphic nonsense mutations that disrupt the active site of the protein. In the extremely rare event when both nonsense mutations are absent, the predicted protein would contain a complete acetyltransferase domain and would be identical in length to NAT8. [provided by RefSeq, Apr 2022]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO22505 | NAT8B Knockout cell line (HeLa) | Human | NAT8B | 1:3~1:6 | Negative | Online Inquiry |
KO22506 | NAT8B Knockout cell line (HCT 116) | Human | NAT8B | 1:2~1:4 | Negative | Online Inquiry |
KO22507 | NAT8B Knockout cell line (HEK293) | Human | NAT8B | 1:3~1:6 | Negative | Online Inquiry |
KO22508 | NAT8B Knockout cell line (A549) | Human | NAT8B | 1:3~1:4 | Negative | Online Inquiry |
NAT8B Gene Knockout Cell Lines are genetically engineered cellular models specifically designed to study the impact of the NAT8B gene in various biological processes. The NAT8B gene encodes a protein involved in amino acid metabolism, particularly within the context of the liver, and disruptions in its expression have been implicated in metabolic disorders and hepatic diseases. By creating knockout models whereby the NAT8B gene has been inactivated, researchers can investigate the function of this gene in cellular contexts and elucidate its role in disease mechanisms.
The key mechanism of action of these cell lines involves the precise deletion of the NAT8B gene using CRISPR-Cas9 technology, ensuring a targeted disruption without affecting adjacent gene regions. This allows for sensitivity in experimental setups to assess the resulting phenotypic changes, such as variations in cellular metabolism, proliferation, and response to drug treatments. The knockout cell line serves as a powerful tool in both basic research and drug discovery, helping to identify metabolic pathways affected by NAT8B and potential therapeutic targets within those pathways.
The scientific importance of NAT8B gene knockout cell lines extends beyond mere gene function elucidation; they have valuable applications in pharmacological studies, modeling diseases related to metabolic dysregulation, and advancing our understanding of liver biology. Compared to traditional wild-type cell lines, these knockout models offer unparalleled insights into gene function through the observation of distinct phenotypes in a controlled environment.
What distinguishes NAT8B gene knockout cell lines from alternatives is their specificity and ease of use in laboratory settings, allowing researchers to efficiently explore the genetic contributions to complex biological processes. These cell lines not only facilitate advanced genetic screenings but also support translational research efforts aimed at developing novel therapeutic interventions.
For researchers and clinicians invested in metabolic studies or liver-related diseases, NAT8B gene knockout cell lines present a vital resource that can significantly accelerate the pace of discovery and innovation. By leveraging our expertise in genetic engineering and cell line development, we aim to provide high-quality biological tools that empower the scientific community to achieve groundbreaking findings.
Please note that all services are for research use only. Not intended for any clinical use.
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