This protocol is no longer in use see the latest notebook here.

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1. Starting The Cell Culture.
2. Protocol for Preparing Adherent Cells 3T3 and HEK293
3. Protocol for Preparing Suspension Cells K562

Preparation for Starting The Cell Culture

• I found this Playlist very helpful. I recommend watching all these videos before you start.
• At least 4 days before the experiment start your cell culture with 3T3 and HEK293 or K562 cells.
• Its good to have a large number of preserved stocks for Future Experiments.
• We started the culture from premade Cell stocks preserved in Complete Growth Media and 7% DMSO.
• The Complete Growth Media used for all Cells lines was DMEM with 10% Fetal Bovine Serμm (FBS) and 1% Pen-Strep.
• For the main experiments we also prepared DMEM with 1% Pen-Strep Only.
• All the Media was made using Aseptic Technique inside a Cell Culture Hood.

Protocol for Starting Cell Culture:

• Disinfect the Cell Culture Hood with 70% Ethanol and Turn on the UV.
• Preheat your Complete Growth media(Eg. DMEM with 10%FBS and 1%PEN-STREP) in a water bath set to 37°C. Wait for 15 minutes.
• Aseptically add 9 ml of warm media to 15ml Tubes labeled with the HEK293 and 3T3 or K562.
• Now quickly thaw your preserved Vials of 3T3 and HEK293 or K562 in the water bath.
  • Shake the Cells in the Water Bath till all the Ice has disappeared.
• Spray down the Vials throughly with 70% Ethanol.
• Aseptically, transfer the Liquid in the Vials to their labeled 15ml Tube.
• Spin down the Cells at 500xg for Five Minutes. Spray with 70% Ethanol.
• Carefully remove the supernatant without disturbing the Cell Pellets.
• Spray your hands with Ethanol between handling each Cell line.
• Resuspend the Cells in 5ml of Complete Growth Media.
• Now Transfer the Cells to labelled Cell Culture Flasks. Label the Flasks with your Name, the Date, the Cell line name and the Media used to Grow the Cells.
• Add additional 30ml of Complete Growth Media to each flask.
• Put the Flasks in the incubator for four days and keep checking the cells before you start the experiments.

Protocol for Preserving Adherent Cells such as 3T3 and HEK293 in DMSO:

• Put the Complete Growth Media (DMEM with 10%FBS and 1%PEN-STREP), DPBS, and TrypLE express bottles in the 37°C water bath in the Cell culture room.
• Turn on the UV for the Cell cutlure hood and wait 15 minutes before you start.
• Examine your cells under the microscope for Contamination.
• Aseptically remove the Media in the Cell Culture Vessels for 3T3 and HEK293.
• Wash the Cells gently with 10ml of DPBS twice.
• Add 5 ml of TrypLE express to both culture vessels. Make sure there is an even coat on the Cells.
• Place in the incubator for 5 minutes at 37°C.
• Remove the cells and check below the Culture Vessel to see if the Cells are detached completely.
• Swirl the Culture Vessels in Circles to detach all the Cells.
• If the Cell density is very high it might be difficult to break the cells into a single-cell suspension. Put the Cells back into the incubator for an additional 3 minutes of digestion in this case.
• Pipette the Cells up and down using a 5ml pipette to break any remaining chunks.
• Aseptically Transfer the Cells to two 15ml Tubes labeled with the name of the Cell Line on each tube.
• Spin down at 500g for 5 minutues.
• Remove the TrypLE express without disturbing the Cell pellets.
• Aseptically Add 10 ml of Complete Growth Media and resuspend the Cells by pipetting up and down.
• Using Sterile Tips Aseptically Add 700μl of DMSO (472301-100ML) to the Cell Suspension and pipette up and down to mix well.
• Using Sterile Tips Transfer 1ml of this mixture to 10 Sterile Cell preservation Cryo Vials.
  • Label each Vial with your name, the Date and the name of the Cell Line.
• Add these Vials to a Cryopreservation Container.
  • Make sure the Isopropanol(IPA) in the container is fresh. IPA should be replaced after 5 uses.
• Leave the Lid ofthe Cryoperservation Container slightly loose.
• Put this container inside the -80°C freezer.
• Wait 24 hours and then quickly transfer these Cells to your Cell Storage Box in -80°C and/or Liquid Nitrogen Vapor Phase.

Protocol for Preserving Suspension Cells such as K562 in DMSO:

• Turn on the UV for the Cell cutlure hood and wait 15 minutes before you start.
• Examine your cells under the microscope for Contamination.
• Evenly resuspend the Cells.
• Aseptically Transfer 10ml Cell Suspension to a 15ml Falcon Tube labeled with the name of the Cell Line.
• Using Sterile Tips Aseptically Add 700μl of DMSO (472301-100ML) to the Cell Suspension and pipette up and down to mix well.
• Using Sterile Tips Transfer 1ml of this mixture to 10 Sterile Cell preservation Cryo Vials.
  • Label each Vial with your name, the Date and the name of the Cell Line.
• Add these Vials to a Cryopreservation Container.
  • Make sure the Isopropanol(IPA) in the container is fresh. IPA should be replaced after 5 uses.
• Leave the Lid ofthe Cryoperservation Container slightly loose.
• Put this container inside the -80°C freezer.
• Wait 24 hours and then quickly transfer these Cells to your Cell Storage Box in -80°C and/or Liquid Nitrogen Vapor Phase.

Protocol for Preparing 5% BSA Solution in DPBS

• Measure 1 gram of BSA powder in a 50ml Falcon Tube.
• Prepare a second 50ml Falcon Tube with 5ml of DPBS.
• Using a 10ml Pipette add 5ml of DPBS to the Falcon tube with BSA powder. Pipette up and down to mix well.
• Wash the contents of the Pipette with the 5ml DPBS in the Second Falcon Tube.
• Add this washed 5ml DPBS to the BSA Solution using the same Pipette.
• Discard the Pippete.
• Close the Falcon Tube and Vortex it at Full Speed.
• Spin down the Tube to reduce bubbles and vortex again till you see no solid particles.
• Make the Final Volume 20ml to make a 5% BSA Solution.
• Load this 5%BSA Solution into a Syringe with a 0.45μm Syringe Filter.
• Filter this BSA Solution into a new 50ml Falcon Tube.

TO DO: Take a Video or Picture on how to do this filtration.

• Be very careful not to introduce particles in the BSA Solutions from this point onwards.
• Store Aliquots of 1ml at -20°C in eppies.

Protocol for Preparing LPS Solution

• Work aseptically inside the Cell Culture Hood.
• To a Syringe add a 23g Needle.
  • Suck up 1ml of Air into the Syringe
• Prepare a Sterile Eppendorf tube with 1ml of Sterile DPBS.
• Suck up 1ml of DPBS from the Eppendorf tube into the Syringe after this.
• Now insert the Syringe Needle into the LPS Vial and inject all the Liquid into the Vial.
• Raise the Needle so it is not dipped into the Liquid and allow it to suck up some of the Air inside the Vial.
  • The additional Air pressure inside the Vial will force the air into the Syringe.
• Once the pressure has equalized, remove the Syringe Needle from the Vial.
• Shake the Vial to mix the DPBS and LPS evenly.
  • You should now have 1mg/ml of LPS dissolved in the DPBS.
• Vortex the Vial at full speed to evenly mix the LPS.
• Prepare an eppendorf tube for depositing the 1mg/ml LPS Solution.
• Using a new Syringe and Needle suck up 2ml of Air inside the Cell Culture hood.
• Inject the air inside the LPS Vial while keeping the Syringe needle immersed in the liquid.
  • The additional air pressure inside the Vial will push the Liquid inside the Vial into the Syringe.
• Deposit this liquid into the Eppendorf tube you prepared earlier.
• Make 50μl Aliquots and store at -20°C.

Protocol for Preparing TNFAlpha Solution:

• Work aseptically inside the Cell Culture Hood.
• Add 1ml of 1ml of Sterile DPBS to the TNFAlpha Vial.
• Vortex at full speed to mix well.
• Spin down the Vial and Store Aliquots of 50μl at -20°C.

Protocol for Preparing Adherent Cells such as 3T3 and HEK for Production Experiments:

• Recipe for DMEM-BSA:
  • 1X DMEM
  • 1%PEN-STEP
  • 0.02% BSA

The purpose of DMEM-BSA is to prevent the Cells from sticking to each other. Using a higher concentration of BSA might interfere with droplet breakage.

Prepare Media For Priming and Flushing Cell Channel of Chrono-Seq Device

• Put the DMEM with 1% PEN-STEP Only, DMEM with 1% PEN-STEP and 10%Fetal Bovine Serum(FBS) DPBS, and TrypLE express bottles in the 37°C water bath in the Cell culture room.
• Thaw one Aliquot of 5%BSA in DPBS on your bench. Protect the BSA from UltraViolet(UV) Light.
• Turn on the UV for the Cell cutlure hood and wait 15 minutes before you start.
• You need about 5ml of media for each timepoint or injection. So for 16 Timepoints you will need about 80ml combined for the Flush containers. Increase this volume for experiments with more timepoints/injections.

• Inside the Cell Culture Hood. Prepare between 100-150ml of DMEM-BSA depending on the number of timepoints/injections for your experiment.
  • Using 5% BSA and DMEM with 1%PEN-STEP make fresh DMEM-BSA (0.02% BSA).
  • Filter this DMEM-BSA with a 40μm Cell Strainer

Always make DMEM-BSA Fresh before the Experiment. Do not make Stocks in Advance!

• Label and Transfer Filtered Liquid to 50ml Tubes for Chrono-Seq Device:
  • Label two Sterile/Particle-Free 50ml Falcon Tubes: Cell Media Flush Reservoir: DMEM-BSA
  • Transfer between 25ml-50ml each to the two 50ml Falcon Tubes depending on number of timepoints/injections for the Cell Media Flush Reservoirs.
  • Label three separate Sterile/Particle-Free 50ml Falcon Tubes Cell Sample Reservoir 1: DMEM-BSA, Cell Sample Reservoir 2: DMEM-BSA, and Cell Sample Reservoir 3.: DMEM-BSA
  • Transfer 15ml each to these three 50ml Falcon Tubes for the Cell Sample Reservoirs.
• Store these 5 Falcon Tubes in Tube racks on your Bench for loading into the Chrono-Seq Device.

Cell Suspension Preparation and Regrowing Cell Surface Receptors

• Examine your cells under the microscope for Contamination.
• Remove the Media in the Cell Culture Vessels for 3T3 or HEK293.
• Wash the Cells gently with 10ml of DPBS two times.
  • This step is to get rid of all the FBS(Fetal Bovine Serum).
  • When washing make sure you don't detach the cells. Avoid detachment by not directly dispensing liquid over the cells.
• Add 5 ml of TrypLE express to both culture vessels. Make sure there is an even coat on the Cells.
• Place in the incubator for 5 minutes at 37°C.
• Remove the cells and check below the Culture Vessel to see if the Cells are detached completely.
• Swirl the Culture Vessels in Circles to detach all the Cells.
• If the Cell density is very high it might be difficult to break the cells into a single-cell suspension. Put the Cells back into the incubator for an additional 3 minutes of digestion in this case.
• Pipette the Cells up and down using a 5ml pipette to break any remaining chunks.
• Transfer the Cells to two 15ml Tubes labeled with the name of the Cell Line on each tube.
• Spin down at 500g for 5 minutues.
• Remove the TrypLE express without disturbing the Cell pellets.
• Using a 5ml Pipette, resuspend in 5ml of DMEM with 10%FBS and 1% PEN-STEP.
• Now add another 5ml each to the 15ml tubes.
• Label one 50ml Tube with the name of the Cell line.
• Filter the cells using a 40μm Cell strainer

Location of Magnetic Stirrers	Pouch with Magnetic Stirrers

• Add a Clean Magnetic Stirring Disk to another 50ml Falcon Tube and add 30ml of DMEM with 10%FBS and 1% PEN-STEP to it. Label this Tube as : HEK293 Suspension for Regrowth of Cell Surface Proteins
• Add the Filtered HEK293 Cell Suspension to this new tube and mix well with the pipette.
• Load this suspension into Cell Reservoir 1 and execute keep_suspension() schedule for 5 hours here.

Make a FBS-Free Cell Suspension after 5 hours

• Freshly Prepare enough Volume of DMEM-BSA for the remaining steps below. To prepare DMEM-BSA:
  • Use 5% BSA and DMEM with 1%PEN-STEP make fresh DMEM-BSA (0.02% BSA).
  • Filter this DMEM-BSA with a 40μm Cell Strainer
• Get the Cell Suspension from the Cell Reservoir 1. Replace the Tube with the DMEM-BSA that was loaded earlier.
• Inside the Cell Culture hood use a Magnet to Remove the magnetic stirring disk from the Cell Suspension.

TO DO Take a Picture or Video on How to Do This.

• Throughly Clean the Magnetic Stirring Disk with 70% Ethanol.
• Dry this Magnetic Stirring Disk using Particle Free Cleanroom Wipes or Paper Towels.
• Keep this Magnetic Stirring Disk inside the Cell Culture Hood on a Cleanroom wipe or Paper Towel.
• Spin down at 500g for 5 minutues.
• Wash the Cells Thrice using DMEM-BSA:
  • Remove most of the media in the Falcon Tube without Disturbing the Cell Pellet.
  • Resuspend the Cells in 25 ml of DMEM-BSA.
  • Spin down at 500g for 5 minutes.
  • Remove most of the media in the Falcon Tube without Disturbing the Cell Pellet.
  • Resuspend the Cells in 25 ml of DMEM-BSA.
  • Spin down at 500g for 5 minutes.
  • Remove most of the media in the Falcon Tube without Disturbing the Cell Pellet.
  • Resuspend the Cells in 10 ml of DMEM-BSA.
• Filter the cells using a 40μm Cell strainer.
• Pipette up and down to make sure the cells have a uniform concentration. Using a P1000, make a 1/20 Dilution using Sterile Tips in a 1.5ml Eppendorf Tube. Do this by adding 50μl of Cell Suspension to 950μl of DMEM-BSA.
• Mix the 1/20 Dilution throughly using the P1000 by pipetting up and down at least 5 times. This is to make sure the Cells have a uniform concentration. Now you can count the cells.
• Add 20μl of the 1/20 Dilution using a P20 to a Fuchs-Rosenthal Hemocytometer. Count at least 5 squares of the Fuchs-Rosenthal Hemocytometer.
• We need a final concentration of 600 cells/μl for Bulk or 215 cells/μl for Single-Cell. Make the Calculation for getting this final concentration.
• Since each Square of the Hemocytometer is 0.2μl. Five squares should give you the Concentration in the 1/20 Dilution per μl. Multiply this number by 20 to get the Approximate concentration in your Cell Stock in cells/μl.
• Make 40ml of HEK293 at 600cells/μl for Bulk Time-Series or 215 cells/μl for Single-Cell Experiments in DMEM-BSA. Calculate how much volume of cells is needed to make the this final dilution. Make sure the cells have a uniform concentration before making this final dilution.
• Remember to Label the Tube with the Name of the Cell Line, Date, Media:DMEM-BSA, Concentration of Cells, and Volume.

✶ OPTIONAL NOTE: You can make the Same Calculation for a Different Cell Concentration and Volumes if you wish.

• Add the Clean/Particle Free Magnetic Stirring Disk to another 50ml Falcon Tube and add 40ml of HEK293 suspension to it. Label this Tube as : HEK293 Suspension, Cell Reservoir 1, 40ml Total Volume

Location of Magnetic Stirrers	Pouch with Magnetic Stirrers

• You are now ready to run the Machine.

Protocol for Preparing Adherent Cells such as 3T3 and HEK for QC Experiments:

• Recipe for DMEM-BSA:
  • 1X DMEM
  • 1%PEN-STEP
  • 0.02% BSA

The purpose of DMEM-BSA is to prevent the Cells from sticking to each other. Using a higher concentration of BSA might interfere with droplet breakage.

Prepare Media For Priming and Flushing Cell Channel of Chrono-Seq Device

• Put the DMEM with 1% PEN-STEP Only, DPBS, and TrypLE express bottles in the 37°C water bath in the Cell culture room. Remember we need NO Fetal Bovine Serum (FBS) in our media for these experiments.
• Thaw one Aliquot of 5%BSA in DPBS on your bench. Protect the BSA from UltraViolet(UV) Light.
• Turn on the UV for the Cell cutlure hood and wait 15 minutes before you start.
• You need about 5ml of media for each timepoint or injection. So for 16 Timepoints you will need about 80ml combined for the Flush containers. Increase this volume for experiments with more timepoints/injections.

• Inside the Cell Culture Hood. Prepare between 100-150ml of DMEM-BSA depending on the number of timepoints/injections for your experiment.
  • Using 5% BSA and DMEM with 1%PEN-STEP make fresh DMEM-BSA (0.02% BSA).
  • Filter this DMEM-BSA with a 40μm Cell Strainer

Always make DMEM-BSA Fresh before the Experiment. Do not make Stocks in Advance!

• Label and Transfer Filtered Liquid to 50ml Tubes for Chrono-Seq Device:
  • Label two Sterile/Particle-Free 50ml Falcon Tubes: Cell Media Flush Reservoir: DMEM-BSA
  • Transfer between 25ml-50ml each to the two 50ml Falcon Tubes depending on number of timepoints/injections for the Cell Media Flush Reservoirs.
  • Label three separate Sterile/Particle-Free 50ml Falcon Tubes Cell Sample Reservoir 1: DMEM-BSA, Cell Sample Reservoir 2: DMEM-BSA, and Cell Sample Reservoir 3.: DMEM-BSA
  • Transfer 15ml each to these three 50ml Falcon Tubes for the Cell Sample Reservoirs.
• Store these 5 Falcon Tubes in Tube racks on your Bench for loading into the Chrono-Seq Device.

✶ Note: You don't need to prepare this media if you won't be using the ChronoSeq Device for your experiment.

Cell Suspension Preparation

• Freshly Prepare enough Volume of DMEM-BSA for the remaining steps below. To prepare DMEM-BSA:
  • Use 5% BSA and DMEM with 1%PEN-STEP make fresh DMEM-BSA (0.02% BSA).
  • Filter this DMEM-BSA with a 40μm Cell Strainer
• Examine your cells under the microscope for Contamination.
• Remove the Media in the Cell Culture Vessels for 3T3 and HEK
• Wash the Cells gently with 10ml of DPBS two times.
  • This step is to get rid of all the FBS(Fetal Bovine Serum).
  • When washing make sure you don't detach the cells. Avoid detachment by not directly dispensing liquid over the cells.
• Add 5 ml of TrypLE express to both culture vessels. Make sure there is an even coat on the Cells.
• Place in the incubator for 5 minutes at 37°C.
• Remove the cells and check below the Culture Vessel to see if the Cells are detached completely.
• Swirl the Culture Vessels in Circles to detach all the Cells.
• If the Cell density is very high it might be difficult to break the cells into a single-cell suspension. Put the Cells back into the incubator for an additional 3 minutes of digestion in this case.
• Pipette the Cells up and down using a 5ml pipette to break any remaining chunks.
• Transfer the Cells to two 15ml Tubes labeled with the name of the Cell Line on each tube.
• Spin down at 500g for 5 minutues.
• Remove the TrypLE express without disturbing the Cell pellets.
• Using a 5ml Pipette, resuspend in 5ml of DMEM-BSA. Use DMEM-BSA for the remaining steps as well from now onwards.
• Now add another 5ml each to the 15ml tubes.
• Label two 50ml Tubes with the name of the Cell lines.
• Filter the cells using a 40μm Cell strainer.
• Pipette up and down to make sure the cells have a uniform concentration. Using a P1000, make a 1/20 Dilution using Sterile Tips in a 1.5ml Eppendorf Tube. Do this by adding 50μl of Cell Suspension to 950μl of DMEM-BSA.
• Mix the 1/20 Dilution throughly using the P1000 by pipetting up and down at least 5 times. This is to make sure the Cells have a uniform concentration. Now you can count the cells.
• Add 20μl of the 1/20 Dilution using a P20 to a Fuchs-Rosenthal Hemocytometer. Count at least 5 squares of the Fuchs-Rosenthal Hemocytometer.
• We need a final concentration of 215 cells/μl for both 3T3 and HEK. Make the Calculation for getting this final concentration.
• Since each Square of the Hemocytometer is 0.2μl. Five squares should give you the Concentration in the 1/20 Dilution per μl. Multiply this number by 20 to get the Approximate concentration in your Cell Stock in cells/μl.
• Make 50ml of 3T3 and 50ml of HEK @ 215 cells/μl in DMEM-BSA. Calculate how much volume of cells is needed to make the this final dilution. Make sure the cells have a uniform concentration before making this final dilution.
• Remember to Label the Tubes with the Name of the Cell Line, Date, Media:DMEM-BSA , Concentration of Cells, and Volume.

✶ OPTIONAL NOTE: You can make the Same Calculation for a Different Cell Concentration and Volumes if you wish.

For Species Mixing Experiment Using ChronoSeq Device:

• Make 50ml of a 50:50 Mix of 3T3 and HEK293 Cells by mixing 25ml of 3T3 and 25ml of HEK293 made in the previous step.
• Throughly Clean the Magnetic Stirring Disk with 70% Ethanol.
• Dry this Magnetic Stirring Disk using Particle Free Cleanroom Wipes or Paper Towels.
• Keep this Magnetic Stirring Disk inside the Cell Culture Hood on a Cleanroom wipe or Paper Towel.
• Add a Clean/Particle Free Magnetic Stirring Disk to another 50ml Falcon Tube and add 35ml of 50:50 Mix to it. Label this Tube as : 3T3:HEK 50:50 Mix, Cell Reservoir 1, 35ml Total Volume

Location of Magnetic Stirrers	Pouch with Magnetic Stirrers

• You are now ready to run the Machine.

Protocol for Preparing Suspension Cells such as K562

• Recipe for DMEM-BSA:
  • 1X DMEM
  • 1%PEN-STEP
  • 0.02% BSA

The purpose of DMEM-BSA is to prevent the Cells from sticking to each other. Using a higher concentration of BSA might interfere with droplet breakage.

Prepare Media For Priming and Flushing Cell Channel of Chrono-Seq Device

• Put the DMEM with 1% PEN-STEP Only bottle in the 37°C water bath in the Cell culture room. Remember we need NO Fetal Bovine Serum (FBS) in our media for these experiments.
• Thaw one Aliquot of 5%BSA in DPBS on your bench. Protect the BSA from UltraViolet(UV) Light.
• Turn on the UV for the Cell cutlure hood and wait 15 minutes before you start.
• You need about 5ml of media for each timepoint or injection. So for 16 Timepoints you will need about 80ml combined for the Flush containers. Increase this volume for experiments with more timepoints/injections.

• Inside the Cell Culture Hood. Prepare between 100-150ml of DMEM-BSA depending on the number of timepoints/injections for your experiment.
  • Using 5% BSA and DMEM with 1%PEN-STEP make fresh DMEM-BSA (0.02% BSA).
  • Filter this DMEM-BSA with a 40μm Cell Strainer

Always make DMEM-BSA Fresh before the Experiment. Do not make Stocks in Advance!

• Label and Transfer Filtered Liquid to 50ml Tubes for Chrono-Seq Device:
  • Label two Sterile/Particle-Free 50ml Falcon Tubes: Cell Media Flush Reservoir: DMEM-BSA
  • Transfer between 25ml-50ml each to the two 50ml Falcon Tubes depending on number of timepoints/injections for the Cell Media Flush Reservoirs.
  • Label three separate Sterile/Particle-Free 50ml Falcon Tubes Cell Sample Reservoir 1: DMEM-BSA, Cell Sample Reservoir 2: DMEM-BSA, and Cell Sample Reservoir 3.: DMEM-BSA
  • Transfer 15ml each to these three 50ml Falcon Tubes for the Cell Sample Reservoirs.
• Store these 5 Falcon Tubes in Tube racks on your Bench for loading into the Chrono-Seq Device.

✶ Note: You don't need to prepare this media if you won't be using the ChronoSeq Device for your experiment.

Cell Suspension Preparation

• Freshly Prepare enough Volume of DMEM-BSA for the remaining steps below. To prepare DMEM-BSA:
  • Use 5% BSA and DMEM with 1%PEN-STEP make fresh DMEM-BSA (0.02% BSA).
  • Filter this DMEM-BSA with a 40μm Cell Strainer
• Examine your cells under the microscope for Contamination.
• Aseptically transfer your cells to a Sterile 50ml Falcon Tube.
• Spin down at 500g for 5 minutues.
• Wash the Cells Thrice using DMEM-BSA:
  • Remove most of the media in the Falcon Tube without Disturbing the Cell Pellet.
  • Resuspend the Cells in 25 ml of DMEM-BSA.
  • Spin down at 500g for 5 minutes.
  • Remove most of the media in the Falcon Tube without Disturbing the Cell Pellet.
  • Resuspend the Cells in 25 ml of DMEM-BSA.
  • Spin down at 500g for 5 minutes.
  • Remove most of the media in the Falcon Tube without Disturbing the Cell Pellet.
  • Resuspend the Cells in 10 ml of DMEM-BSA.
• Filter the cells using a 40μm Cell strainer.
• Pipette up and down to make sure the cells have a uniform concentration. Using a P1000, make a 1/20 Dilution using Sterile Tips in a 1.5ml Eppendorf Tube. Do this by adding 50μl of Cell Suspension to 950μl of DMEM-BSA.
• Mix the 1/20 Dilution throughly using the P1000 by pipetting up and down at least 5 times. This is to make sure the Cells have a uniform concentration. Now you can count the cells.
• Add 20μl of the 1/20 Dilution using a P20 to a Fuchs-Rosenthal Hemocytometer. Count at least 5 squares of the Fuchs-Rosenthal Hemocytometer.
• We need a final concentration of 215 cells/μl for K562. Make the Calculation for getting this final concentration.
• Since each Square of the Hemocytometer is 0.2μl. Five squares should give you the Concentration in the 1/20 Dilution per μl. Multiply this number by 20 to get the Approximate concentration in your Cell Stock in cells/μl.
• Make 50ml of K562 at 215 cells/μl in DMEM-BSA. Calculate how much volume of cells is needed to make the this final dilution. Make sure the cells have a uniform concentration before making this final dilution.
• Remember to Label the Tube with the Name of the Cell Line, Date, Media:DMEM-BSA, Concentration of Cells, and Volume.

✶ OPTIONAL NOTE: You can make the Same Calculation for a Different Cell Concentration and Volumes if you wish.

For Experiment Using ChronoSeq Device:

• Throughly Clean the Magnetic Stirring Disk with 70% Ethanol.
• Dry this Magnetic Stirring Disk using Particle Free Cleanroom Wipes or Paper Towels.
• Keep this Magnetic Stirring Disk inside the Cell Culture Hood on a Cleanroom wipe or Paper Towel.
• Add a Clean/Particle Free Magnetic Stirring Disk to another 50ml Falcon Tube and add 40ml of K562 suspension to it. Label this Tube as : K562 Suspension, Cell Reservoir 1, 40ml Total Volume

Location of Magnetic Stirrers	Pouch with Magnetic Stirrers

• You are now ready to run the Machine.