Gene: RUNX1
Official Full Name: RUNX family transcription factor 1provided by HGNC
Gene Summary: Core binding factor (CBF) is a heterodimeric transcription factor that binds to the core element of many enhancers and promoters. The protein encoded by this gene represents the alpha subunit of CBF and is thought to be involved in the development of normal hematopoiesis. Chromosomal translocations involving this gene are well-documented and have been associated with several types of leukemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO04631 | RUNX1 Knockout cell line (HeLa) | Human | RUNX1 | 1:3~1:6 | Negative | Online Inquiry |
KO04632 | RUNX1 Knockout cell line (HCT 116) | Human | RUNX1 | 1:2~1:4 | Negative | Online Inquiry |
KO04633 | RUNX1 Knockout cell line (HEK293) | Human | RUNX1 | 1:3~1:6 | Negative | Online Inquiry |
KO04634 | RUNX1 Knockout cell line (A549) | Human | RUNX1 | 1:3~1:4 | Negative | Online Inquiry |
RUNX1 Gene Knockout Cell Lines are engineered cell lines specifically designed to disable the RUNX1 gene, a crucial transcription factor involved in hematopoiesis and immune system regulation. By utilizing CRISPR-Cas9 gene editing technology, these cell lines provide a powerful tool for researchers seeking to elucidate the role of RUNX1 in various biological processes, including cell differentiation, apoptosis, and tumorigenesis.
The primary function of RUNX1 involves the regulation of gene expression during the development of blood cells. By knocking out this gene, researchers can study the consequent cellular and molecular alterations, providing insights into hematological disorders, cancers, and immune-related diseases. These cell lines enable scientists to investigate the mechanistic pathways that lead to conditions such as acute myeloid leukemia and other malignancies, thereby enhancing our understanding of cancer biology and potential therapeutic targets.
The scientific significance of RUNX1 knockout cell lines extends into both research and clinical settings. In research, they serve as vital tools for functional studies, enabling detailed investigations into gene function and interaction networks. Clinically, insights gained from studies using these cell lines could lead to the development of targeted therapies aimed at restoring proper RUNX1 function or compensating for its deficiency in disease contexts.
One of the key advantages of our RUNX1 knockout cell lines is their precise genetic modification, which provides a reliable and consistent experimental model. Unlike traditional knockout methods, CRISPR-Cas9 technology ensures specific deletions without off-target effects, resulting in more accurate and reproducible data. Additionally, these cell lines are available in various backgrounds, allowing researchers to select the most suitable model for their specific studies.
For researchers, clinicians, and institutions aiming to advance their understanding of hematopoiesis and related pathologies, the RUNX1 Gene Knockout Cell Lines are invaluable assets. They facilitate groundbreaking discoveries that can influence diagnostics and therapeutic strategies. Backed by our company's extensive experience in genetic engineering and commitment to innovation, we provide quality products that meet the high standards of the scientific community, empowering research and clinical advancements alike.
Please note that all services are for research use only. Not intended for any clinical use.
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