Babco, Signet, Sternberger Monoclonals, Senetek, Covance

ELISA/assay

Zombie UV™ Fixable Viability Kit

423107

100 tests

83 USD

423107

Zombie UV™ Fixable Viability Kit

Fixable Dye, Fixable Viability Dye

100 tests

83 USD

NONAB_CHMPRB

Standard Cell Staining Protocol: Prior to reconstitution, spin down the vial of lyophilized reagent in a microcentrofuge to ensure the reagent is at the bottom of the vial. For reconstitution, pre-warm the kit to room temperature; add 100 ul of DMSO to one vial of Zombie UV dye and mix until fully dissolved Wash cells with PBS buffer (no Tris buffer and protein free). Dilute Zombie UV dye at 1:100-1000 in PBS. Resuspend 1-10 x 10 6 cells in diluted 100 ul Zombie UV solution. To minimize background staining of live cells, titrate the amount of dye and/or number of cells per 100 ul for optimal performance. Different cell types can have a wide degree of variability in staining based on cell size and degree of cell death. Note: Don t use Tris buffer as a diluent and be sure that the PBS does not contain any other protein like BSA or FBS. Note: The amount of dye used can also influence the ability to detect apoptotic as well as live and dead cells. Incubate the cells at room temperature, in the dark, for 15-30 minutes. Wash one time with 2 ml BioLegend s Cell Staining Buffer (Cat. No. 420201) or equivalent buffer containing serum or BSA. Continue performing antibody staining procedure as desired. Cells can be fixed with paraformaldehyde or methanol prior to permeabilization or can be analyzed without fixation. . No-wash Sequential Staining Protocol: Wash cells with PBS buffer (no Tris buffer and protein free). For reconstitution, pre-warm the kit to room temperature; add 100 ul of DMSO to one vial of Zombie UV dye and mix until fully dissolved Determine the total ul volume of antibody cocktail previously titrated and optimized for the assay that will be added to each vial/well of cells based on a final volume of 100 ul. Subtract that antibody volume from the 100 ul total staining volume intended for the assay. In the remaining volume, dilute Zombie UV dye at 1:100-1000 in PBS as determined by prior optimization at that volume. For example, if you are adding 20 ul of antibody cocktail for a 100 ul total staining volume, use 80 ul of Zombie UV solution. Resuspend 1-10 x 10 6 cells in the appropriate volume of Zombie UV solution. Different cell types can have a wide degree of variability in staining based on cell size and degree of cell death. Note: Don t use Tris buffer as a diluent and be sure that the PBS does not contain any other protein like BSA or FBS. Note: The amount of dye used can also influence the ability to detect apoptotic as well as live and dead cells. Incubate for 10-15 minutes at RT, protected from light. Without washing the cells, add the cell surface antibody cocktail and incubate for another 15-20 minutes. Add 1-2 mL Cell Staining Buffer (Cat. No. 420201) or equivalent buffer containing BSA or serum. Centrifuge to pellet. Continue with normal fixation and permeabilization procedure. If planning to skip fixation and analyze cells live, complete an additional wash step to minimize any unnecessary background of the live cells. . Notes: If the cell type in use cannot tolerate a protein-free environment, then titrate the Zombie UV dye in the presence of the same amount of BSA/serum as will be present in the antibody staining procedure. A higher amount of Zombie UV may be required since the BSA/serum will react with and bind up some proportion of the Zombie UV . Zombie UV dye is excited by the UV laser (350 nm) and has fluorescence emission maximum at 459 nm. If using in a multi-color panel design, filter optimization may be required depending on other fluorophores used. Zombie UV dye has similar emission to DAPI. .