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Creative Biogene supplies customers with an overall microbiological research program: including sample collection, preservation methods, preliminary experiments and effect evaluation, experiments and data analysis, etc.

Creative Biogene supplies customers with an overall microbiological research program: including sample collection, preservation methods, preliminary experiments and effect evaluation, experiments and data analysis, etc.

Creative Biogene supplies customers with an overall microbiological research program: including sample collection, preservation methods, preliminary experiments and effect evaluation, experiments and data analysis, etc.

Creative Biogene supplies customers with an overall microbiological research program: including sample collection, preservation methods, preliminary experiments and effect evaluation, experiments and data analysis, etc.

Baseceuticals provides customized CRISPR/Cas9 service to accelerate gene editing project and gene and cell therapies research.

RNA interference (RNAi) and antisense oligonucleotide (ASO) are the two most commonly used strategies for silencing gene expression. Both two methods are used for targeting of RNAs involved in distinct diseases.

RNA interference is a technique that can be used to silence specific genes that related to disease. RNAi is tended to have the greatest effect as a therapeutic method in cancer and infectious diseases. The application of RNAi has significance in gene therapy and drug development.

The usage of antisense oligonucleotides is a promising method to gene silencing. Generally, the antisense oligonucleotides are regarded as therapeutic agents for the regulating of specific genes at the post-transcriptional level.

IntegrateRNA provides one stop solution for lncRNA research, including lncRNA sequencing, microarray-based expression profiling analysis, lncRNA qPCR, lncRNA knockdown, and lncRNA knockout.

To support the recent emerging of circular RNA (LncRNA) research, IntegrateRNA provides a fast, one-stop LncRNA sequencing solution.

IntegrateRNA provides one stop service for miRNA research, including miRNA discovery, confirmation, functional analysis, target validation, mechanism analysis to in vivo experiment.

IntegrateRNA offers complete microRNA sequencing services including RNA preparation and quality control, library construction, sequencing, and comprehensive data analysis, producing the results needed to rapidly advance biological and biomedical research.

Creative Biogene specializes in providing comprehensive and advanced organic acid fermentation technologies.

Creative Biogene specializes in providing comprehensive and advanced vitamins fermentation technologies.

Creative Biogene specializes in providing comprehensive and advanced steroids fermentation technologies.

Creative Biogene is committed to providing you with the best CRISPR/Cas9 based microbe genome editing services. Tell us how can we help you today.

Creative Biogene has launched a powerful QVirus™ Platform for Lentivirus, Retrovirus, Adeno-associated Virus (AAV), Adenoviruses, Retrovirus, Oncolytic virus, etc.

Recombinant adeno-associated viral (rAAV) vectors have been used in over 200 clinical trials with a good safety profile and significant clinical benefit in a number of genetic diseases. Moreover, because of their ability to infect non-dividing and dividing cells and to act as an efficient substrate for homologous recombination, rAAVs are being used as a tool for gene-editing approaches.

Lentiviral vector stocks are tested for the presence of RCL through monitoring p24 antigen expression in the culture medium of transduced 293T cells. Serial passaging of the transduced p24 cells over this period allows for the amplification of RCL. This method is used to assess the presence of RCR in lentiviral preparations.

QVirus™ Platform provides lentivirus production services to study the different stages of autophagy flux, making the autophagy study much easier. Our lentiviral biosensors enable convenient transduction of easy- and hard-to-transfect cell types with fluorescently-tagged proteins of interest. These packaged lentiviral particles provided higher efficiency of gene delivery and more homogeneous expression of introduced proteins compared to non-viral transfection methods. If you have any special requirements, please feel free to contact us.