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HBE1 Knockout Cell Lines

Gene: HBE1

Official Full Name: hemoglobin subunit epsilon 1provided by HGNC

Gene Summary: The epsilon globin gene (HBE) is normally expressed in the embryonic yolk sac: two epsilon chains together with two zeta chains (an alpha-like globin) constitute the embryonic hemoglobin Hb Gower I; two epsilon chains together with two alpha chains form the embryonic Hb Gower II. Both of these embryonic hemoglobins are normally supplanted by fetal, and later, adult hemoglobin. The five beta-like globin genes are found within a 45 kb cluster on chromosome 11 in the following order: 5'-epsilon - G-gamma - A-gamma - delta - beta-3' [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO37411 HBE1 Knockout cell line (HCT 116) Human HBE1 1:2~1:4 Negative Online Inquiry
KO37412 HBE1 Knockout cell line (A549) Human HBE1 1:3~1:4 Negative Online Inquiry

Background

HBE1 Gene Knockout Cell Lines represent a powerful tool in molecular biology, specifically designed to facilitate the study of gene function and the underlying mechanisms of disease. These cell lines have been engineered using CRISPR/Cas9 gene editing technology to selectively disrupt the HBE1 gene, which encodes the human hemoglobin beta chain. As a result, researchers can observe the phenotypic consequences of gene knockout, providing insights into the pathological factors associated with hemoglobin disorders and enabling further exploration of therapeutic interventions.

The primary function of HBE1 Gene Knockout Cell Lines revolves around their ability to mimic the genetic conditions found in various hematological diseases. By generating precise deletions in the targeted gene, these cell lines allow for the investigation of altered cellular behaviors, including changes in erythropoiesis, hemoglobin synthesis, and response to oxidative stress. Through functional assays, researchers can assess the effects of genetic inactivation and understand the biological roles of the HBE1 gene in cellular homeostasis and disease progression.

The scientific importance of these cell lines is underscored by their broad applications in fundamental research, drug discovery, and the development of gene therapies. They serve as a critical platform for studying genetic mutations involved in blood disorders such as β-thalassemia and sickle cell anemia, paving the way for personalized medicine approaches. Additionally, these cell lines can be instrumental in validating novel therapeutic targets and in screening compounds that might correct or compensate for the loss of gene function.

Distinct from traditional cell lines, HBE1 Gene Knockout Cell Lines offer a unique advantage by providing precise genetic context that mimics human disease more accurately. This specificity enhances the reliability of research findings and reduces the translational gap between laboratory experiments and clinical applications. Moreover, the utility of these cell lines is amplified by their compatibility with various high-throughput screening methods, enabling accelerated research timelines.

For researchers and clinicians focused on hemoglobinopathies and other genetic disorders, the HBE1 Gene Knockout Cell Lines are invaluable assets. They empower scientific inquiry by offering insight into gene-disease relationships, thereby facilitating the development of innovative treatments and therapies.

Our company has extensive expertise in the development of specialized biological products, offering a diverse portfolio of high-quality cell lines and genetic models that support cutting-edge research endeavours. With a commitment to advancing scientific discovery, we provide products that resonate with the evolving needs of researchers and healthcare professionals alike.

Please note that all services are for research use only. Not intended for any clinical use.

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