Gene: ASXL1
Official Full Name: ASXL transcriptional regulator 1provided by HGNC
Gene Summary: This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO20862 | ASXL1 Knockout cell line (HeLa) | Human | ASXL1 | 1:3~1:6 | Negative | Online Inquiry |
KO20863 | ASXL1 Knockout cell line (HCT 116) | Human | ASXL1 | 1:2~1:4 | Negative | Online Inquiry |
KO20864 | ASXL1 Knockout cell line (HEK293) | Human | ASXL1 | 1:3~1:6 | Negative | Online Inquiry |
KO20865 | ASXL1 Knockout cell line (A549) | Human | ASXL1 | 1:3~1:4 | Negative | Online Inquiry |
ASXL1 Gene Knockout Cell Lines are genetically modified cellular models designed to facilitate the study of the ASXL1 gene's function, a critical regulator involved in various biological processes, including chromatin remodeling and gene expression regulation. The specific knockout of the ASXL1 gene in these cell lines allows researchers to investigate its role in hematopoiesis, development, and disease, particularly in cancers such as acute myeloid leukemia and myelodysplastic syndromes, where ASXL1 mutations are frequently implicated.
The primary function of these cell lines is to provide a controlled environment for investigating the downstream effects of ASXL1 loss of function. By employing CRISPR/Cas9 and other gene editing technologies, the ASXL1 Gene Knockout Cell Lines enable scientists to explore pathways affected by ASXL1 deficiency, assess changes in cellular behavior, and uncover potential therapeutic targets. Researchers can pinpoint alterations in gene expression profiles, cellular proliferation rates, and differentiation capabilities, thus gleaning insights into the molecular mechanisms that drive tumorigenesis.
The scientific importance of these models cannot be overstated; ASXL1 Gene Knockout Cell Lines are instrumental for basic research and translational studies aimed at understanding the pathology of ASXL1-related disorders. Their application ranges from drug discovery to biomarker identification, making them invaluable tools for both academic research laboratories and clinical investigations.
What sets our ASXL1 Gene Knockout Cell Lines apart from alternatives is their exceptional quality and reliability. Manufactured using stringent quality control measures, these cell lines are validated for consistent performance and reproducibility, ensuring that researchers can obtain accurate, replicable data. Additionally, our dedicated customer support team provides assistance throughout the research process, enhancing user experience and satisfaction.
For researchers and clinicians seeking to delve into the intricacies of ASXL1-related biology, the ASXL1 Gene Knockout Cell Lines are a vital resource. They not only aid in elucidating the gene's role but also bolster efforts to develop targeted therapies that can significantly impact patient outcomes. Leveraging years of expertise in genetic research, our company is committed to providing high-quality biological products that empower the scientific community in their quest for knowledge and innovation.
Please note that all services are for research use only. Not intended for any clinical use.
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