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  • Enhancing biomarker discovery with SMART-Seq Pro kit and ICELL8 cx system
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Home › Learning centers › Automation systems › ICELL8 introduction › Technical notes › ICELL8 cx system reagent formulation and dispense guidelines

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Reagent formulation and dispensing with CELLSTUDIO Software on the ICELL8 cx system

  • Best practices for dispensing reagents
  • Reagent test parameters
  • Additive tables

ICELL8 cx CELLSTUDIO v2.6 Software (CELLSTUDIO Software) allows researchers to innovate and develop new applications for the ICELL8 cx Single-Cell System. The system's open format gives users greater control of cell selection, reagent formulation, and reagent and sample dispensing for downstream processing.

Developing new applications may involve dispensing novel reagents that need to be tested to ensure they have minimal cross-contamination and can be precisely dispensed prior to being incorporated into a workflow. To assist with this process, Takara Bio scientists have generated guidelines for reagent formulation and dispensing. We have tested commonly used additives such as Polyethylene Glycol 8000 (PEG 8000), glycerol, Triton X-100, NP-40, Tween-20, and SDS to address these concerns.

The guidelines below are intended to help researchers save time in their application development efforts without compromising confidence in their data.

When to use these guidelines

These guidelines are only necessary when developing your own custom applications for the ICELL8 cx Single-Cell System using CELLSTUDIO Software. The ICELL8 cx Single-Cell System User Manual (Appendix G, "Designing an Application: Advice from Our Scientists") notes when these guidelines are applicable.

Blank ICELL8 cx chips and additional consumables which should be used during custom application development and usage are available for order from their product page.

If you're an ICELL8 cx Instrument user and haven't yet upgraded to CELLSTUDIO Software, you can request an upgrade from Technical Support or have it upgraded during an onsite service visit. Purchases of an ICELL8 cx Instrument in 2020 or later will have CELLSTUDIO Software preinstalled.

NOTE: Reagent dispensing has already been calibrated for the Takara Bio prevalidated ICELL8 cx applications; these guidelines should NOT be applied to those procedures.

Best practices for dispensing reagents

  1. When dispensing a reagent that has a high concentration of detergent and/or viscous additives, it is best to observe how cleanly the reagent dispenses. A user can observe the blotting paper to see how much of the liquid dispensed was on top of the chip. Ideally, there should be little to moderate blotted area on the paper.

    Figure 1. Examples of blotting paper illustrating a range of dispense quality. These images can be used as a reference for your dispenses to help evaluate the quality. Left image. The red circles indicate where spots were found. The number and small size indicate a good dispense. Center image. The blue circles again mark where damp spots were found. Slightly larger, this dispense is considered within acceptable parameters. Right image. With this much liquid absorbed by the paper, the dispense would be considered 'poor'.

  2. After the dispense, users should use [Stream Check] (under the Advanced tab of CELLSTUDIO Software) to flush out the system lines. Following the stream check, users should perform 2–3 tip clean cycles. Performing an alcohol prime is also recommended if the tips still do not seem clean. See the user manual for the steps on how to do these two processes.

Reagent test parameters

All reagents used in testing were at room temperature.

Average dispense volume test

We measured the density of the reagent using a scale that goes to 0.0001 g, sensitive enough to accurately measure the volume dispensed. We dispensed the reagent into an Single-Cell 250f Chip (Cat. # 640193) and recorded the weight before and after blotting the chip. Using the measured density, we calculated the average dispense volume. We considered the dispense successful if there was no large area of liquid blotted off the chip, and the average dispense volume was within 10% of the expected volume.

Satellite droplet test

We prepared reagents with a 1:200 dilution of a UV-reactive dye. We dispensed onto Single-Cell chips in a checkerboard pattern and imaged the chips afterward on a SmartChip ND Real-Time PCR Cycler. We counted the instances of satellite droplets on top of the chip that can pose a risk for contamination. We considered the dispense to have passed if the total number of satellite droplets was less than 3–4% of the total number of dispensed wells.

Test guidelines

We have provided two sets of concentration ranges based on these tests. Users can decide what concentration range to follow when dispensing based on their concerns.

Example: Following the ranges based solely on the average dispense volume test is not recommended for dispenses when cross-contamination would be an issue (e.g., index dispense).

However, if cross-contamination is not a significant concern and the user just wants to ensure the dispense volume is accurate (e.g., PCR master mix dispense), following the ranges based only on the average dispense volume test is fine.

Passing concentrations

  • We define "minimum passing concentration" as the lowest concentration that was tested during this study and passed the criteria established for the given test. We have not tested concentrations lower than this limit. While dispensing a reagent below this concentration limit may be fine, the user would do so at their own risk.
  • We define "maximum passing concentration" as the highest concentration that was tested during this study and passed the criteria established for the given test. In most cases, we also tested concentrations higher than this limit, and they failed the criteria established in the protocol. We would not recommend users go beyond the maximum passing concentration benchmark.

Summary

When formulating reagents for a novel in-chip application on CELLSTUDIO Software, users should determine how compatible the additive concentrations are with the ICELL8 cx system. An ideal in-chip dispense would have limited cross-contamination between wells and accurate dispense volumes. We have taken these concerns into consideration when developing this application note. Users can follow the concentration ranges established from this study to facilitate a smoother transition from in-tube reactions to in-chip reactions without having to frequently reformulate the reagents.

Minimum/maximum concentration ranges for tested additives

Viscous additives: PEG 8000, glycerol

PEG 8000

Concentration ranges based on satellite droplet test
Dispense volume settingMinimum concentration*Maximum concentration*
35 or 50 nl 2.5% 17.5%
100 nl 2.5% 10%
Concentration ranges based only on the average dispense volume test
Dispense volume settingMinimum concentration*Maximum concentration*
35 or 50 nl 1% 17.5%
100 nl 1% 10%

*All percentages are based on weight/volume % (w/v).

Glycerol

Concentration ranges based on satellite droplet test
Dispense volume settingMinimum concentration†Maximum concentration†
35 nl 2.5% 7.5%
50 nl 2.5% 30%
100 nl 2.5% 7.5%
Concentration ranges based only on the average dispense volume test
Dispense volume settingMinimum concentration†Maximum concentration†
35, 50, or 100 nl 1% 40%

†All percentages are based on volume/volume percent (v/v).

Non-ionic detergents: NP-40, Triton X-100, Tween-20

NP-40

Concentration ranges based on satellite droplet test
Dispense Volume SettingMinimum concentration†Maximum concentration†
35 or 50 nl 0.1% 2%
100 nl 0.1% 0.5%
Concentration ranges based only on the average dispense volume test
Dispense Volume SettingMinimum concentration†Maximum concentration†
35, 50, or 100 nl 0.1% 2%

†All percentages are based on volume/volume percent (v/v).

Triton X-100

Concentration ranges based on satellite droplet test
Dispense volume settingMinimum concentration†Maximum concentration†
35 nl 0.1% 1%
50 nl 0.1% 2%
100 nl 0.1% 0.8%
Concentration ranges based only on the average dispense volume test
Dispense volume settingMinimum concentration†Maximum concentration†
35, 50, or 100 nl 0.1% 2%

†All percentages are based on volume/volume percent (v/v).

Tween-20

Concentration ranges based on satellite droplet test
Dispense volume settingMinimum concentration†Maximum concentration†
35 nl 0.1% 2%
50 nl 0.1% 5%
100 nl 0.1% 1%
Concentration ranges based only on the average dispense volume test
Dispense volume settingMinimum concentration†Maximum concentration†
35, 50, or 100 nl 0.1% 5%

†All percentages are based on volume/volume percent (v/v).

Anionic detergents: SDS

SDS

Concentration ranges based on satellite droplet test
Dispense volume settingMinimum concentration*Maximum concentration*
35 nl 0.05% 0.8%
50 nl 0.03% 0.8%
100 nl 0.01% 0.05%
Concentration ranges based only on the average dispense volume test
Dispense volume settingMinimum concentration*Maximum concentration*
35 or 50 nl 0.01% 0.8%
100 nl 0.01% 0.1%

*All percentages are based on weight/volume percentage (w/v).

Viscous additives & non-ionic detergent in combination, based on satellite droplet test

Glycerol & non-ionic detergent in combination

35 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40% 35 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40% 35 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40%
0.1% Triton X‑100 0.1% Tween‑20 0.1% NP‑40
1% Triton X‑100 2% Tween‑20 2% NP‑40

 

50 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40% 50 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40% 50 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40%
0.1% Triton X‑100 0.1% Tween‑20 0.1% NP‑40
2% Triton X‑100 2% Tween‑20 2% NP‑40

 

100 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40% 100 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40% 100 nl Glycerol 10% Glycerol 20% Glycerol 30% Glycerol 40%
0.8% Triton X‑100 0.1% Tween‑20 0.5% NP‑40
1% Triton X‑100 1% Tween‑20 2% NP‑40

Figure 2. Test results combining glycerol and detergent in various volumes and concentration percentages. Blue cells mean the row/column concentration combination test passed the criteria; orange means it failed.

PEG 8000 & non-ionic detergent in combination

35 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5% 35 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5% 35 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5%
0.1% Triton X‑100 0.1% Tween‑20 0.1% NP‑40
1% Triton X‑100 2% Tween‑20 2% NP‑40

 

50 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5% 50 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5% 50 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5%
0.1% Triton X‑100 0.1% Tween‑20 0.1% NP‑40
2% Triton X‑100 2% Tween‑20 2% NP‑40

 

100 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5% 100 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5% 100 nl PEG 8000 2.5% PEG 8000 7.5% PEG 8000 12.5% PEG 8000 17.5%
0.8% Triton X‑100 0.1% Tween‑20 0.5% NP‑40
1% Triton X‑100 1% Tween‑20 2% NP‑40

Figure 3. Test results combining PEG 8000 and detergent in various volumes and concentration percentages. Blue cells mean the row/column concentration combination test passed the criteria; orange means it failed.


Basic cell preparation for the ICELL8 cx system

Takara Bio generated basic cell preparation guidelines and suggestions for staining and dispensing on the ICELL8 cx system.

Read more

Protocol: Preparation of adult mouse cardiomyocytes for the ICELL8 system

Learn how to isolate cardiomyocytes from adult mouse heart in preparation for ICELL8 experiments.

Read more

Protocol: Nuclei isolation from mammalian cells

Learn how to isolate nuclei from mammalian cells in preparation for ICELL8 experiments.

Read more

Flexibility to isolate cells of any size is critical to single-cell analysis

View the growing list of cell types that have been isolated on the ICELL8 Single-Cell System.

Read more

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