Cell Insert

·Innovative hanging design facilitates pipetting.

·Supplied in multiple well plates: 6-well, 12-well, 24well.

·PC membrane: low adsorption rate, reducing the loss of small molecular proteins and other compounds

·Transparent PET inserts permit sufficient optical transparency for visualization of cell outlines by phase contrast microscopy. 

· Transparent PET membrane is easy to observe.

·The PC membrane is not easy to be torn or curled, and it is easy to operate when taking out the chamber.

·Compatible with most solvents used for fixing and dyeing.

Attention：

• Attachment of cells grown on a permeable support (membrane) is sensitive to the initial seeding density, so the initial use should be inoculated with different density guarantee optimal growth;

•During the cultivation process, the liquid should be taken through the gap between the upper layer and the hole. When adding liquid, be careful and slow to avoid the damage of the membrane;

•Incubation of the permeable support in the medium prior to culturing the cells can improve cell attachment and distribution.

Guidelines for us：

• Pre-equilibration: After added culture solution to the pores of the multi-well plate and inserted the insert, please placed it in the incubator for at least one hour or overnight. 

• Fix and stain cells directly in the nest, and use a scalpel to cut the membrane for long-term storage. Before using please add culture solution to the pores of the multi-well plate, then insert the insert and add the culture solution which included cells to the insert.

• Before using please add culture solution to the pores of the multi-well plate, then insert the insert and add the culture solution which included cells to the insert.

• Pre-equilibration: After added culture solution to the pores of the multi-well plate and inserted the insert, please placed it in the incubator for at least one hour or overnight.

• Check the volume of the culture medium regularly and add fresh medium as needed.

• The cell layer can be directly fixed and stained in the nest using basic cytological methods. Note Avoid using solvents that dissolve the PC film.

• Fix and stain cells directly in the nest, and use a scalpel to cut the membrane for long-term storage.

Before using please add culture solution to the pores of the multi-well plate, then insert the insert and add the culture solution which included cells to the insert.