Description
METHODS FOR FIXATION, STAINING, AND ANALYZING APO-BRDU™ SAMPLES Fixation Protocol This is a standard protocol used at BD Biosciences Pharmingen for quality control testing of the APO-BRDU™ Kit. Cell fixation using paraformaldehyde is a required step in the APO-BRDU™ assay. The following cell fixation procedure is a suggested method. Variables such as cell origin and growth conditions can affect the results. The fixation conditions provided below should be considered as guidelines. Additional experimentation may be required to obtain results comparable to the control cells provided with this kit. The positive and negative control cells provided in the APO-BRDU™ Kit are already fixed. 1. Suspend the cells in 1% (w/v) paraformaldehyde in PBS (pH 7.4) at a concentration of 1-2 x 10^6 cells/ml. 2. Place the cell suspension on ice for 30-60 minutes. 3. Centrifuge cells for 5 min at 300 x g and discard the supernatant. 4. Wash the cells in 5 ml of PBS, then pellet the cells by centrifugation. Repeat the wash and centrifugation. 5. Resuspend the cell pellet in the residual PBS in the tube by gently vortexing the tube. 6. Adjust the cell concentration to 1-2 x 10^6 cells/ml in 70% (v/v) ice cold ethanol. Let cells stand for a minimum of 30 min on ice or in the freezer. See note below. 7. Store cells in 70% (v/v) ethanol at -20°C until use. Cells can be stored at -20°C several days before use. Note: In some biological systems, storage of the cells at -20°C in 70% (v/v) ethanol for at least 12-18 hr prior to staining for apoptosis detection yields the best results. Cells can be stored at -20°C for several months before use. Staining Protocol The following protocol describes the method for measuring apoptosis in the positive and negative control cells that are provided in the APO-BRDU™ Kit. The same procedure should be employed for measuring apoptosis in the cell specimens provided by the researcher. 1. Resuspend the positive (51-6577LZ) and negative (51-6578LZ) control cells by swirling the vials. Remove 1 ml aliquots of the control cell suspensions (approximately 1 x 10^6 cells/ml) and place in 12 x 75 mm flow cytometry centrifuge tubes. Centrifuge the control cell suspensions for 5 min at 300 x g and remove the 70% (v/v) ethanol by aspiration, being careful to not disturb the cell pellet. 2. Resuspend each tube of control cells with 1.0 ml of Wash Buffer (51-6579AZ) for each tube. Centrifuge as before and remove the supernatant by aspiration. 3. Repeat the Wash Buffer treatment (Step 2). 4. Resuspend each tube of the control cell pellets in 50 µl of the DNA Labeling Solution (prepared as described below). DNA Labeling Solution 1 Assay 5 Assays 10 Assays Reaction Buffer (green cap) 10.00 µl 50.00 µl 100.00 µl TdT Enzyme (yellow cap) 0.75 µl 3.75 µl 7.50 µl Br-dUTP (violet cap) 8.00 µl 40.00 µl 80.00 µl Distilled H2O 32.25 µl 161.25 µl 322.50 µl Total Volume 51.00 µl 255.00 µl 510.00 µl *The appropriate volume of DNA Labeling Solution to prepare for a variable number of assays is based upon multiples of the component volumes needed for 1 assay. Mix only enough DNA Labeling Solution to complete the number of assays prepared per session. The DNA Labeling Solution is active for approximately 24 hr at 4°C. 5. Incubate the cells in the DNA Labeling Solution for 60 min at 37°C in a temperature-controlled bath. Shake cells every 15 min to resuspend. Note: The DNA Labeling Reaction can also be carried out at RT overnight for the control cells. For samples other than the control cells provided in the kit, incubation times at 37°C may need to be adjusted to longer or shorter periods depending on the requirements of the cells supplied by the researcher. 6. At the end of the incubation time, add 1.0 ml of Rinse Buffer (51-6583AZ) to each tube and centrifuge each tube at 300 x g for 5 min. Remove the supernatant by aspiration. 7. Repeat the cell rinsing (as in Step 6) wi th 1.0 m l of th e Rinse B uffer, centr ifuge, and remove th e supernatant by aspiration. 8. Resuspend the cell pellet in 0.1 ml of the Antibody Staining Solution (prepared as described below). 9. Incubate the cells with the FITC-labeled anti-BrdU Antibody Solution in the dark for 30 min at RT. 10. Add 0.5 ml of the PI/R Nase Stainin g Buffer (51-6585 AZ) to the tube containing the 0.1 ml Antibody Staining Solution. Antibody Staining Solution 1 Assay 5 Assays 10 Assays FITC-Labeled Anti-BrdU (orange cap) 5.00 µl 25.00 µl 50.00 µl Rinsing Buffer (red cap) 95.00 µl 475 µl 950.00 µl Total Volume 100.00 µl 500.00 µl 1000 µl Note: If the cell density is low, decrease the amount of PI/RNase Staining Buffer to 0.3 ml. 11. Incubate the cells in the dark for 30 min at RT. 12. Analyze the cells in PI/RNase Staining Buffer by flow cytometry. Analyze the cells within 3 hr of staining to obtain optimal results. Cells may begin to deteriorate if left overnight before analysis. Analyzing APO-BRDU™ Samples by Flow Cytometry This assay is run on a flow cytometer equipped with a 488 nm Argon laser as the light source. Expected results using the positive and negative control cells are shown in Figs. 1-3. Propidium iodide (PI; total cellular DNA) and FITC (apoptotic cells) are the two dyes being used. PI fluoresces at about 623 nm and FITC at 520 nm when excited at 488 nm. No fluorescence compensation is required. Two dual parameter and two single parameter displays are created with the flow cytometer data acquisition software. The gating display should be the standard dual parameter DNA doublet discrimination display with the DNA Area signal on the Y-axis and the DNA Width on the X-axis, (Fig. 1). From this display, a gate is drawn around the non-clumped cells and the second gated dual parameter display is generated. The normal convention of this display is to put DNA (Linear Red Fluorescence) on the X-axis and the FITC-BrdU (Log Green Fluorescence) on the Y-axis. Two single parameter gated histograms, DNA and FITC-BrdU, can also be added but are not necessary. By using the dual parameter display method, not only are apoptotic cells resolved but their cell cycle stage is also determined. TECHNICAL TIPS AND FREQUENTLY ASKED QUESTIONS 1. For those researchers using adherent cell lines, the cells in the supernatant have a higher probability of being apoptotic than do the adherent cells. Save cells in the supernatant for use in the assay prior to trypsinization of the adherent cell layer. 2. Cell fixation using a DNA cross-linking chemical fixative (e.g. paraformaldehyde) is an important step in analyzing apoptosis by this method. Unfixed cells may lose smaller fragments of DNA that are not chemically fixed in place inside the cell prior to washing steps. The researcher may have to explore alternative fixation and permeablization methods to fully exploit their systems. 3. A cytospin or centrifugal cytology slide can be prepared from the APO-BRDU™ sample in the following manner: After completion of the FITC-labeled anti-BrdU antibody staining, but prior to the PI/RNase treatment, put a drop of the stained cells on a slide, spin it and observe the sample under a fluorescence microscope. 4. To minimize cell loss during the assay, we recommend the use of 12 x 75 mm polystyrene tubes throughout the staining procedure and analysis. With other types of tubes or plastics (e.g. polypropylene), cells may build up on the sides of the tubes, resulting in significant loss of cell numbers, as well as inefficient staining of those cells which are not fully exposed to staining reagents. We also recommend that following wash steps, cells be resuspended by gentle mixing and not by pipetting, as plastic pipette tips can also contribute to cell loss throughout the assay. 5. Occasionally, a mirror image population of cells at lower intensity is observed in the flow cytometry dual parameter display. This population arises during the 50 µl DNA Labeling Reaction, when some cells become stuck to the side of the test tube and are not fully exposed to the Labeling Solution. This phenomenon can be overcome by washing all the cells from the side of the tube and making sure all cells are properly suspended at the beginning of the labeling reaction. 6. If a low intensity of FITC staining is observed, try increasing the incubation time during the 50 µl DNA Labeling Reaction. Labeling times of up to 4 hr at 37°C may be required for certain cell systems. 7. If DNA cell cycle information is not required, it is not necessary to add the PI/RNase Staining Buffer to the samples. Warning: Reaction Buffer (component 51-6580AZ) contains 0.2% Cacodylic acid (w/w). Hazard Statements: May cause cancer. Precautionary Statements: Obtain special instructions before use. Do not handle until all safety precautions have been read and understood. Wear protective clothing / eye protection Wear protective gloves IF exposed or concerned: Get medical advice / attention Store locked up. Dispose of contents / container in accordance with local / regional / national / international regulations Danger: Negative Control Cells (component 51-6578LZ) and Positive Control Cells (component 51-6577LZ) contains 56.0% ethanol (w/w). Hazard statements Highly flammable liquid and vapor. Causes serious eye irritation. Precautionary statements Keep away from heat/sparks/open flames/hot surfaces. No smoking. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Store in a well-ventilated place. Keep cool. Dispose of contents/container in accordance with local/regional/national/international regulations.
1. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
2. Please refer to http://regdocs.bd.com to access safety data sheets (SDS).
3. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
