RayBio Annexin V-Cy5 Apoptosis Detection Kit

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RayBio Annexin V-Cy5 Apoptosis Detection Kit User Manual Version 1.0 Mar 20, 2014 (Cat#: 68C5-AnnV-S) RayBiotech, Inc. We Provide You With Excellent Support And Service Tel:(Toll Free)1-888-494-8555 or 770-729-2992; Fax:770-206-2393; Web: www.raybiotech.com Email: info@raybiotech.com

RayBiotech, Inc. Kit TABLE OF CONTENTS I. Introduction. 1 II. Reagents. 2 III. Assay Protocol... 2 IV. General Troubleshooting Guide... 4 I. INTRODUCTION Annexin V Apoptosis Detection Kit is based on the observation that soon after initiating apoptosis, cells translocate the membrane phosphatidyl-serine (PS) from the inner face of the plasma membrane to the cell surface. Once on the cell surface, PS can be easily detected by staining with a fluorescent conjugate of Annexin V, a protein that has a high affinity for PS. The one-step staining procedure takes only 10 minutes. Detection can be analyzed by flow cytometry or by fluorescence microscopy. 1

II. REAGENTS Components 68C5-AnnV- S25 68C5-AnnV- S100 68C5-AnnV- S400 Part Number 25 assays 100 assays 400 assays Annexin V-Cy5 125 µl 500 µl 2 ml Item A 1X Binding Buffer 12.5 ml 50 ml 2 x 100 ml Item B III. ASSAY PROTOCOL A. Incubation of cells with Annexin V-Cy5: 1. Induce apoptosis by desired method. 2. Collect 1-5 x 10^5 cells by centrifugation. 3. Resuspend cells in 500 µl of 1X Annexin V Binding Buffer. 4. Add 5 µl of Annexin V-Cy3. 5. Incubate at room temperature for 5 min in the dark. 6. Proceed to B or C below depending on method of analysis. B. Quantification by Flow Cytometry: Analyze cells by flow cytometry (Ex = 649 nm; Em = 670 nm) using a Helium- Neon Laser. For adherent cells, trypsinize and gently wash cells with serum-containing medium before incubation with Annexin V-Cy5 (A.3-5). C. Detection by Fluorescence Microscopy: 1. Place the cell suspension from Step A.5 on a glass slide. Cover the cells with a glass coverslip. For analyzing adherent cells, grow cells directly on a coverslip. Following incubation (A.5), invert coverslip on a glass slide and visualize cells. The cells 2

can also be washed with 1X Annexin V binding Buffer and fixed in 2% formaldehyde before visualization. (Cells must be incubated with Annexin V- Cy5 before fixation because any cell membrane disruption can cause nonspecific binding of annexin V to PS on the inner surface of the cell membrane.) 2. Observe the cells under a fluorescence microscope using Cy5 filter, or FITC/Cy3/Cy5 triple band filter (Chroma Technology) if performing triple labeling using these dyes, or detect cells using a CCD camera. Cells that have bound Annexin V-Cy5 will show bright red-blue staining on the plasma membrane. 3

V. GENERAL TROUBLESHOOTING GUIDE Problems Cause Solution High Background Lower signal levels Erratic results Cell density is higher than Refer to datasheet and use the suggested cell recommended number Increased volumes of Use calibrated pipettes accurately components added Incubation of cell samples for Refer to datasheets and incubate for exact extended periods times Use of extremely confluent cells Perform assay when cells are at 80-95% confluency Contaminated cells Check for bacteria/ yeast/ mycoplasma contamination Washing cells with PBS Always use binding buffer for washing cells before/after fixation (adherent cells) Cells did not initiate apoptosis Determine the time-point for initiation of apoptosis after induction (time-course experiment) Very few cells used for analysis Refer to data sheet for appropriate cell number Incorrect setting of the Refer to datasheet and use the recommended equipment used to read samples filter setting Use of expired kit or improperly Always check the expiry date and store the stored reagents components appropriately Uneven number of cells seeded Seed only healthy cells (correct passage in the wells number) Adherent cells dislodged at the Perform experiment gently and in duplicates time of experiment or triplicates for each treatment Incorrect incubation times or Refer to datasheet & verify correct incubation temperatures times and temperatures Incorrect volumes used Use calibrated pipettes and aliquot correctly Increased or random staining Always stain cells with Annexin before observed in adherent cells fixation (makes cell membrane leaky) Note: The most probable cause is listed under each section. Causes may overlap with other sections. 4

This product is for research use only. 2004 RayBiotech, Inc. 5