Hanheng Biotechnology (Shanghai) Co., Ltd.
CRISPR/Cas9
Hanbio offers gene delivery solutions and have been focusing on virus packaging for more than ten years, we also pay attention to the research field of autophagy, CRISPR/Cas9 and non-coding RNA. As a R & D enterprise, Hanbio has independently developed reagent products, including molecular and cellular reagents.
Basics about Virus Packaging
Basics about Virus Packaging

Viral vectors are modified viruses that can carry and deliver genes into target cells and animals. During the virus packaging process, the desired genetic material is inserted into the viral vector, which is then propagated in host cells to produce a high quantity of the modified virus. The resulting viral particles can then be used to deliver the genetic material into specific cells or tissues for various purposes, such as gene therapy or genetic engineering.


Virus packaging plays a crucial role in gene delivery as it allows researchers to use viruses as vehicles to introduce specific genes into cells and tissues, thereby manipulating their genetic makeup or function. This technique has significant applications in biomedical research, including the development of therapeutic treatments for genetic disorders and the study of cellular processes and disease mechanisms.

Featured Hanbio Virus Packaging
Featured Hanbio Virus Packaging
Lentivirus Packaging
Lentiviruses are a type of retrovirus, known for their ability to integrate their genetic material into the host cell's genome. They can infect both dividing and non-dividing cells, making them suitable for long-term gene expression.
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Adenovirus Packaging
Adenoviruses are DNA viruses that can efficiently infect a wide range of dividing and non-dividing cells. Adenoviruses do not integrate their genetic material into the host cell's genome. The infection efficiency of adenovirus is high, which can infect suspension cells and primary cells.
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AAV Adeno Associated Virus Packaging
AAV is a small, non-enveloped virus with a single-stranded DNA genome. AAV is an ideal tool for expressing or modifying genes in a broad range of cell and tissue types, especially in vivo, with high efficiency and enhanced safety.
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Viral Vector Construction
Because of their special targeting specificity and gene delivery properties, viral vectors are frequently used as tools for disease research or as vectors for gene delivery. The three most widely used viral vectors are lentivirus, adenovirus, and adeno-associated virus (AAV).
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Hanbio provides high-quality products and excellent research services, with customers spread across research institutions and pharmaceutical enterprises. So far, there have been over 8000 publications of viral products including journals such as Cell, Nature, Science, Cancer Cell, Nature Medicine, Circulation, etc.
About Hanbio

Hanbio was founded in 2010 and is a high-tech enterprise focused on gene technology research and application transformation, located in Shanghai China. Hanbio has always been committed to the research and production of gene vectors, and our core competitive products include lentiviruses, adenoviruses, and adeno-associated viruses. At the same time, we focus on hot topics, including autophagy flow research tools, virus vector based CRISPR gene editing tools, non-coding RNA, and luciferase experiments.

In the future, we will focus more on the application of core gene technology in clinical transformation.


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