Secondary Antibodies: Buy 1, Get 1 Free
This basic protocol focuses on the measurement of fluorescence intensity produced by fluorescent-labeled antibodies and ligands that bind specific cell-associated molecules.
Fast FACS Buffer: (Code # MB-086-0500, sodium azide assists in preventing capping and shedding or internalization of the antibody-antigen complex after the antibodies bind to the receptors). We suggest using our 10X PBS (Code # MB-008 10X PBS pH 7.2 (0.2 M Potassium Phosphate 1.5 M Sodium Chloride)).
Fixation Buffer: 2% Paraformaldehyde in PBS.
Permeabilization Buffer: 0.1% Triton in PBS.
70% ethanol, stored at -20ºC.
FACs Buffer Products PBS ProductsFITC Products
If it is desired to simultaneously analyze surface and intracellular molecules at single-cell level, staining cell-surface antigen first by following procedure A step 1 to 6, then stain the intracellular antigen by following procedure B. Perform all procedure B steps in dark.
This procedure utilizes ethanol to fix the cells and permeabilize the membrane, which allows the dye (Propidium Iodide) to enter the cells. Propidium Iodide (PI) is a DNA-binding fluorochrome that intercalates in the double-helix. Ribonuclease-A is used to eliminate the staining of double-stranded RNA.
Procedure C can be combined with the procedure A of cell surface antigens analysis. Use only FITC-labeled antibodies for surface antigen, since PI emits in the orange to red region of the spectrum (FITC emits green). Do not fix the cells with paraformaldehyde. Start procedure C after step 6 of procedure A.
Additional FACS Protocol Resources
Rockland Immunochemicals Inc.Gilbertsville, PA 19525E-mail: email@example.comPhone: 800.656.7625