The document provides procedures for priming, running samples, and cleaning a Beckman Z1 Coulter Particle Counter. The priming procedure involves removing the blue Coulter Clenz fluid from the aperture tube using the diluent. Running samples requires loading 100uL samples into vials with diluent, mixing, and taking the average of three readings. The cleaning procedure uses diluent and Coulter Clenz to clean the aperture tube and surrounding areas.
Original Description:
For use with Purdue Chemistry cell culture facility
The document provides procedures for priming, running samples, and cleaning a Beckman Z1 Coulter Particle Counter. The priming procedure involves removing the blue Coulter Clenz fluid from the aperture tube using the diluent. Running samples requires loading 100uL samples into vials with diluent, mixing, and taking the average of three readings. The cleaning procedure uses diluent and Coulter Clenz to clean the aperture tube and surrounding areas.
The document provides procedures for priming, running samples, and cleaning a Beckman Z1 Coulter Particle Counter. The priming procedure involves removing the blue Coulter Clenz fluid from the aperture tube using the diluent. Running samples requires loading 100uL samples into vials with diluent, mixing, and taking the average of three readings. The cleaning procedure uses diluent and Coulter Clenz to clean the aperture tube and surrounding areas.
The following procedure will be performed utilizing aseptic technique, as
described in Aseptic Techniques Used for Mammalian Cell Culture Priming Machine 1. Turn instrument on. Make sure waste jar is not full, diluent jar is full. a. Be gentle taking machine pieces in and out of the bottles, they will easily fracture. 2. Lower ledge and remove vial with Coulter Clenz (blue), set aside vial. 3. Fill new vial with Z-Pak diluent (20 mL), load vial, and close door. 4. On computer board, press FUNCTION, select PRIME APERTURE, press START twice. a. The machine will run through 9 cycles to remove blue fluid out of aperture tube. 5. After priming, load fresh 10 mL vial of diluent and press SET-UP (check size settings) and press START. a. Cell count readings will be below 100. b. If cell count is larger than 100, repeat step 5. Running Samples 1. Load your samples (100L each) into separate vials containing 9.9 mL diluent. Cap and gently invert vial three times. a. Minimize bubbles produced when mixing, they will be counted. 2. Press START and read each sample three times. 3. Take the average of the three readings for your final count. a. If readings become dissimilar, aperture may be clogged. Use the small, pink brush to clean the opening and repeat readings. *Good dilution readings will be from 3,000-10,000. Cleaning Machine 1. Put fresh 20 mL vial of diluent on shelf, move vial up and down 10 times to clean aperture tube. 2. Press SET-UP (check size settings) and press START. a. Cell count readings will be below 100. b. If cell count is larger than 100, repeat step 2. 3. Place vial with Coulter Clenz (blue) on. 4. Switch off instrument (O=OFF) 5. Empty vials of liquid waste into 10% bleach. a. If liquid waste is at fill line, pour liquid waste into sink. 6. Place empty plastic vials into biohazard waste container. a. If small biohazard container is full, empty into large biohazard container. 7. Spray and wipe down area with 70% Ethanol. 8. Replace red cap on diluent dispenser.