Creative Biolabs has a tradition of commitment. To achieve efficient execution and regulatory approval, we offer careful considerations of your program for the development of a cellular or gene therapy product – now and in the future.
EXPLORE MORE HighlightsWe focus on unmet needs and develop novel cellular and gene drugs and solutions that offer significant benefits over existing options.
EXPLORE MORE HighlightsThe advent of Chimeric Antigen Receptor T-cell (CAR-T) therapies has revolutionized the field of oncology, providing new avenues for treating various forms of cancer. Our 20 years of experience in the biotechnology sector have equipped us with the expertise and technological capabilities to support the entire lifecycle of CAR-T products, from early development to commercialization.
EXPLORE MORETo accelerate advanced breakthroughs of your projects, we offer broad range of platforms which enable our clients be free to tackle problems with cutting-edge technologies from different angles and in different methods.
EXPLORE MORE HighlightsUse the resources in our library to help you understand your options and make critical decisions for your study. We offer oncolytic virus, CAR-T, and dendritic cell related documents, as well as newsletter. If you don't find the answers you're looking for, contact us for additional assistance.
EXPLORE MORE HighlightsGet a real taste and understanding of the business and culture of one of the world's great research-based cellular and gene therapy discovery and development companies.
EXPLORE MOREUniversal CAR-T cell therapies are expected to transform the landscape of cancer immunotherapy and enhance patient results. Creative Biolabs has earned a strong reputation in the field of cellular and gene therapy research, innovation, and advancement. Our team of specialists is committed to advancing novel therapeutic solutions for UCAR-T production aimed at addressing a wide range of cancer types.
Our Universal CAR-T Cell Production Service follows a streamlined workflow that maximizes efficiency and minimizes production costs. The process can be summarized as follows:
UCAR-T derived from peripheral blood mononuclear cells (PBMCs), umbilical cord blood (UCB), and renewable stem cells such as induced pluripotent stem cells (iPSCs) or embryonic stem can be produced.
Various gene editing methods are available, including but not limited to Transcription Activator-like Nucleases (TALEN), Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR/Cas9).
UCAR-T can also be manufactured with non-gene editing methods to minimize the off-target effect induced by gene editing, with which the expression of the target genes were interfered.
UCAR-T can also be manufactured with non-gene editing methods to minimize the off-target effect induced by gene editing, with which the expression of the target genes were interfered.
We offer a range of UCAR-T cell editing strategies designed to enhance their functionality, ultimately making them more efficient at targeting and eradicating cancer cells through various approaches.
Our service offers customization of Universal CAR-T cells for various cancer types. Whether it's hematologic malignancies like leukemia or solid tumors like breast cancer, our team can adapt the Universal CAR-T cells to target the specific antigens associated with the disease.
Please do not hesitate to contact us if you have any questions about the process.
For any technical issues or product/service related questions, please leave your information below. Our team will contact you soon.
All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.
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