The development of in vivo glycobiological disease models aims to gain insight into the pathogenesis and biological characteristics of diseases such as disorders of glucose metabolism. Through the application of advanced technologies such as gene editing, transgenic technology, and embryo implantation and culture, researchers can construct animal models that mimic human diseases, thereby enabling accurate simulation and control of the disease development process. CD BioGlyco provides one-stop Glycobiology Disease Model Development Services to clients based on different technologies. The technologies include but are not limited to the following.
CD BioGlyco employs gene editing technology to accurately alter animal genomes for the creation of in vivo glycobiological models, aiding in the modeling of human diseases and the examination of specific gene functions and roles.
We provide comprehensive transgenic-based in vivo glycobiology disease model development services to our clients. Our team is dedicated to providing reliable and high-quality support in the field of glycobiology.
Embryo Implantation and Cultivation
CD BioGlyco is dedicated to providing high-quality in vivo glycobiology disease model development service based on reliable embryo implantation and cultivation technology. Our emphasis is on precision, and attention to detail.
We perform artificial selection by selecting individuals with specific traits for reproduction to increase or decrease the frequency of these traits in the offspring for targeted construction of glycobiological disease models.
Some diseases are associated with mutations in the activity of specific genes, CD BioGlyco offers gene expression-based in vivo glycobiology disease model development service to your research related to these glycobiology models.
Our glycobiology disease model development services are founded on various technologies, yet the process of these services remains similar.
We typically engage in thorough discussions with the client to gain a comprehensive understanding of the study objectives, disease selection, and anticipated outcomes. Subsequently, we carefully select suitable techniques and models and develop experimental protocols tailored to specific requirements. Following extensive preparatory work, we proceed with the construction of the glycobiological disease model. Finally, we conduct comprehensive data collection and analysis on the constructed disease model, encompassing phenotyping, biochemical index testing, etc., to ensure alignment with expected criteria.
CD BioGlyco possesses a state-of-the-art laboratory and utilizes advanced technologies for the development of in vivo glycobiology disease models. Our team of experts offers comprehensive services tailored to different needs, ensuring the highest quality results. Among them, our experts are skillful in operating knock-in, knockdown, and knock-out gene editing techniques in gene editing, striving to choose the most appropriate technology for your research. Similarly, we have first-class transgenic technologies, including but not limited to adenovirus-mediated transgenesis, transfection of embryonic stem cells, and embryo injection, and we aim to provide clients with the most comprehensive and professional service. In terms of embryo implantation and cultivation-based in vivo glycobiology disease model development, we utilize expertise in embryo transfection technology and embryo transfer techniques to provide reliable results. What's more, RT-qPCR, RNA sequencing, and microarray analysis are used in gene expression to confirm a completed service. Our experts have extensive experience in utilizing these techniques to study the regulation and function of genes in various biological processes. Additionally, they are proficient in data analysis and interpretation, allowing them to extract meaningful insights from complex gene expression datasets.
Technology: Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9)
Journal: Biomedicines
IF: 4.757
Published: 2023
Results: This article examines the advancements and future potential of gene editing in pluripotent stem cells. It emphasizes the significance of utilizing gene editing in human pluripotent stem cells, such as embryonic stem cells and induced pluripotent stem cells, for clinical cell therapy. First, since all mutations in pluripotent stem cells are passed on to their progeny, untargeted editing by editors is amplified. Pluripotent stem cells are highly susceptible to DNA damage, and the double-strand breaks caused by gene editing may result in ineffective editing and an increase in cell populations with compromised genome protection. To avoid these consequences, researchers prefer to use gene editing tools that do not rely on double-strand breaks, such as base-editing enzymes and primitive editing enzymes. In addition, Cas-associated nucleases, transposons, and recombinases are expanding the gene editing toolbox as the microbial world is better understood. The article also discusses current practical applications of gene editing in pluripotent stem cells using programmable nucleases, efforts by researchers to optimize these systems, and new tools that can potentially be used for differentiation modeling.
Fig.1 Gene editing in pluripotent stem cells used in research and medicine. (Zhang, et al., 2023)
Through the establishment of cooperative relationships with pharmaceutical companies and academic institutions around the world, CD BioGlyco is constantly enhancing our knowledge to offer the most extensive technologies for developing in vivo glycobiology disease models. For further details, please don't hesitate to contact us.
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