Astrocyte has a central role in brain development and function and has gained increasing attention over the past two decades. With our well-established STEMOD™ platform, the experienced scientists at Creative Biolabs are dedicated to helping you with astrocyte differentiation service. Our high-quality services will greatly contribute to the success of your projects.
In general, there are two types of culture systems for directed neural differentiation of hESC, including adherent and suspension culture. In a prolonged culture, an embryoid body (EB) can form a multilayered structure and cavities filled with cystic fluid. In addition, a variety of signaling molecules, factors, and conditioned media have been used for directed neural differentiation.
Neural tissue engineering is a promising strategy for neural repair and neurological diseases treatment. In this case, proper preclinical models are required to mimic the micro-environment. Here, Creative Biolabs has developed the STEMOD™ neuroscience ex vivo models for our clients all over the world.
For several decades, CNS diseases have caused serious burdens for individuals with these diseases in both physical and mental health. Studies show that more than 95% of CNS diseases have an unknown etiology, which presents scientists with significant obstacles on the road to the creation of efficient treatments. Parkinson's disease and Alzheimer's disease are the two most common types of...
Australian researchers claimed that they have found a cure for cervical cancer in mice using gene-editing technology, which is a big breakthrough for gene therapy, and Creative Biolabs spares no effort in assisting global scientists to make greater progress.
Earlier this month, scientists from Griffiths University’s Menzies Health Institute Queensland used gene editing technology...
Optic neuropathies are a class of neurodegenerative diseases caused by various reasons such as hypoxia, inflammation, poisoning, nutritional deficiencies, glaucoma, compression, trauma, hereditary and congenital diseases. Although the causes of optic neuropathy have their own characteristics, they will eventually lead to the death of optic ganglion cells (RGCs).
The axons emitted by RGCs...
Recently, hearing of mice with a genetic form of deafness which is similar to a type found in people was restored by a team of international researchers. This brings new hope for people suffering from hearing loss. Will genetic therapy be a new way to heal deafness? A senior scientist of Creative Biolabs explains more about this work.
Why choose gene therapy to do research?
Hearing loss is...
Surgery, radiotherapy, and chemotherapy have always been the main treatment methods for malignant tumors. In recent years, with a deeper exploration of gene technology, the development of molecular targeted therapy and biotherapy has received great attention at home and abroad. Biotherapy combined with traditional treatments has achieved remarkable results in improving the quality...
CAR-T is the short name for Chimeric Antigen Receptor T-Cell Immunotherapy. To put it simply, CAR-T is to transform the patient's immune T cells in vitro to make them recognize the antigens on the surface of tumor cells, and then transfer these cells back to the patient to achieve the therapeutic effect of identifying and killing cancer cells.
In 2017, the US Food and Drug Administration (FDA)...
CAR-T technology was first studied for cancer therapy research. Immunotherapy has become a revolution in the field of cancer treatment. Compared with traditional methods such as radiation and chemotherapy, immunotherapy is more specific with less ity. CAR-T cell therapy is the most promising method among various kinds of immunotherapies, which has shown the ability to eliminate various tumors,...
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