Adeno-associated virus (AAV) is a highly efficient gene therapy vector that is utilized to deliver transgenes to a variety of different tissues in vivo, and it is currently being evaluated for using in the research of acute and chronic lung ...Read more

Fluorescent proteins are often used in our experiments, but how to select the appropriate one? Hopefully this post will give you some recommendation in which fluorescent proteins to choose. Tubes of various fluorescent proteins displayed in ...Read more

Aadeno-associated virus (AAV) have been identifed as a promising means for gene deliver. AAV tropism, as dictated by AAV capsid proteins, is an important factor affecting transduction efficiency and specificity across cell types. Consequentl ...Read more

With the development of viral gene delivery systems, many different viruses are being adapted as vectors to introduce genes into diverse types of cells and tissues, but the most advanced are lentivirus (LV), adenovirus (Ad) and adeno-associa ...Read more

A Highly Effective Transfection Enhancer For LV Introduce This novel transfection enhancer (Enhancer A+B) is composed of liquid A (1000) and liquid B (200). It contains high-valent cationic polymer and cholesterol, which can enhance the per ...Read more

The adeno-associated virus (AAV) vector can efficiently transfects a wide variety of cells and tissues, which are suitable for long term gene expression in non-dividing cells and short term in dividing cells with a low cytotoxicity and immun ...Read more

The eye is the most important organ of the human senses. Compared with other organs, the eye is small, relatively closed and away from other tissues. Eye diseases are complex, and the rise of gene therapy offers hope for the treatment of inh ...Read more

Recombinant adeno-associated virus vector (rAAV) is derived from non-pathogenic wild type adeno-associated virus and has the advantages of good safety and wide host range. rAAV has become a hotspot in gene therapy research, especially in the ...Read more