Gene: BCL11A
Official Full Name: BCL11 transcription factor Aprovided by HGNC
Gene Summary: This gene encodes a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. The corresponding mouse gene is a common site of retroviral integration in myeloid leukemia, and may function as a leukemia disease gene, in part, through its interaction with BCL6. During hematopoietic cell differentiation, this gene is down-regulated. It is possibly involved in lymphoma pathogenesis since translocations associated with B-cell malignancies also deregulates its expression. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO02093 | BCL11A Knockout cell line (HEK293) | Human | BCL11A | 1:3~1:6 | Negative | Online Inquiry |
BCL11A Gene Knockout Cell Lines are genetically modified cellular models designed to facilitate the study of BCL11A, a pivotal regulator of gene expression involved in various biological processes including hematopoiesis and immune response. These cell lines are created by utilizing CRISPR/Cas9 gene-editing technology, enabling precise deletion or inactivation of the BCL11A gene, which allows researchers to investigate the gene's role in disease progression, particularly in hematological malignancies such as sickle cell disease and beta-thalassemia.
The primary function of the BCL11A knockout cell lines is to provide an experimental platform for analyzing the consequences of BCL11A deficiency on cellular pathways, differentiation, and overall cellular function. By observing these mutated cell lines, researchers can uncover critical insights into how BCL11A modulates gene expression, influencing the switch from fetal to adult hemoglobin production, thereby paving the way for potential therapeutic interventions.
Scientifically, these cell lines are invaluable tools in both basic research and clinical applications. They can enhance our understanding of gene regulation and its implications in therapy development targeting BCL11A, offering new avenues for treating genetic blood disorders. Moreover, these models may serve as screening platforms for novel drugs aimed at manipulating BCL11A activity, thus providing significant insights into drug efficacy and safety.
In comparison to traditional models, such as primary tissue samples or non-specific knockdown approaches, BCL11A Gene Knockout Cell Lines deliver specificity, reproducibility, and ease of use. Their consistent genetic background enables clear attribution of phenotypic changes solely to the BCL11A knockout, minimizing unwanted variability and enhancing the reliability of experimental outcomes.
For researchers and clinicians seeking to delve into the complexities of gene regulation and its therapeutic implications, the BCL11A Gene Knockout Cell Lines represent a powerful asset. They stand as a testament to our commitment to delivering advanced, precise biological tools that drive innovation in medical research. With our extensive expertise in genetic engineering and a focus on providing high-quality biological products, we are dedicated to supporting the scientific community in their quest for solutions to unmet medical needs.
Please note that all services are for research use only. Not intended for any clinical use.
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