Gene: WT1
Official Full Name: WT1 transcription factorprovided by HGNC
Gene Summary: This gene encodes a transcription factor that contains four zinc-finger motifs at the C-terminus and a proline/glutamine-rich DNA-binding domain at the N-terminus. It has an essential role in the normal development of the urogenital system, and it is mutated in a small subset of patients with Wilms tumor. This gene exhibits complex tissue-specific and polymorphic imprinting pattern, with biallelic, and monoallelic expression from the maternal and paternal alleles in different tissues. Multiple transcript variants have been described. In several variants, there is evidence for the use of a non-AUG (CUG) translation initiation codon upstream of, and in-frame with the first AUG. Authors of PMID:7926762 also provide evidence that WT1 mRNA undergoes RNA editing in human and rat, and that this process is tissue-restricted and developmentally regulated. [provided by RefSeq, Mar 2015]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05955 | WT1 Knockout cell line (HEK293) | Human | WT1 | 1:3~1:6 | Negative | Online Inquiry |
KO05956 | WT1 Knockout cell line (A549) | Human | WT1 | 1:3~1:4 | Negative | Online Inquiry |
WT1 Gene Knockout Cell Lines refer to genetically modified cell lines where the Wilms' Tumor 1 (WT1) gene has been inactivated or "knocked out." This gene plays a critical role in kidney development and has been implicated in various cancers, including Wilms' tumor, leukemia, and ovarian cancer. The targeted disruption of the WT1 gene in these cell lines provides researchers with a versatile platform for studying the molecular mechanisms of cancer development, as well as potential therapeutic interventions.
These cell lines operate on the principle of gene editing, utilizing CRISPR/Cas9 technology or similar methodologies to achieve precise genetic alterations. By knocking out WT1, researchers can observe changes in cell behavior, differentiation, and response to treatments, thereby unveiling the gene's function in oncogenesis and tumor suppression. The ability to create knockout models is vital for dissecting complex biological pathways and validating drug targets.
The scientific importance of WT1 Gene Knockout Cell Lines is underscored by their applications in both basic research and clinical settings. They serve as invaluable tools in cancer biology, aiding in the understanding of tumorigenesis, the development of novel therapies, and the evaluation of drug efficacy. Their use extends to the investigation of WT1's role in renal physiology and pathology, further enhancing our understanding of kidney diseases.
Compared to alternative models, such as traditional knockout mice or transiently transfected cell lines, WT1 Gene Knockout Cell Lines provide a more convenient, time-efficient, and reproducible approach. They are available in various formats, including different cellular backgrounds which enhance their applicability across diverse research contexts, allowing for specialized study of cell lineage and environment-specific interactions.
For researchers and clinicians focused on genomics, cancer biology, and renal disorders, WT1 Gene Knockout Cell Lines represent a robust resource that can significantly advance their studies. They offer a dynamic system for explorations that can lead to groundbreaking findings in cancer prevention and treatment strategies.
Our company, a leader in biological product innovation, is committed to providing high-quality genetic models, paired with dedicated support and expertise. We ensure that our offerings meet the rigorous standards required for cutting-edge scientific research, empowering our customers to achieve their research goals efficiently and effectively.
Please note that all services are for research use only. Not intended for any clinical use.
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