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4D-Nucleofector™ Manual – 

Bioscience Solutions

   15

2.9  4D-Nucleofector™ X Unit

The 4D-Nucleofector™ X Unit can handle two types of vessels:

 

– 16-well 20 µL Nucleocuvette™ Strips for cell numbers from 2 x 10

4

 to 

1 x 10

6

 cells 

 

– Single 100 µL Nucleocuvette ™ Vessels for cell numbers from 2 x 10

5

 

to 2 x 10

7

 cells

2.9.1 

Defining a New Experiment

1.  After unit and vessel type selection (see chapter 2.8.2) a screen 

appears with the message “Choose Experiment or Position” (figure 
2.13, A). You can now either select a predefined experiment (see 
chapter 2.8.4) or define an experiment from the beginning.

 

By tapping on a position you can select one or multiple samples/wells 
(e.g. A1 and A2) that should be defined with the same parameters. 
The selected positions are highlighted with an orange frame (figure 
2.13, B).

NOTE:  

For the 16-well Nucleocuvette™ Strips, you can select a whole 
column by double clicking on the top or bottom well.  Wells can 
be de-selected by tapping on the position again. The orange frame 
will disappear.

2.  Upon well selection the fields “CELL TYPE PROGRAM”, “CUSTOM 

PROGRAM”, “PULSE CODE”, “SOLUTION” and “CONTROL” will be activated 
(figure 2.13, B). For further explanation about parameters, please refer 
to chapter 2.8.3.

3.  Press the field “CELL TYPE PROGRAM” to choose predefined 

Nucleofection conditions from a cell type list (figure 2.13, C). Use the 
search (magnifying glass symbol) or the sort list functions (A-Z) to 
find conditions more quickly.

a.  Select the desired cell type code by tapping on the appropriate 

line of the cell list. The cell type selected will be highlighted. For 
additional information about the cell type selected press “i”.

b.  To confirm your selection press “OK”.
c.  If required, modify pulse code by pressing the letter or number 

code fields. A keyboard will appear, enabling you to change 
settings. The solution code can be modified via a selection list.

NOTE:  

Instead of defining solution and program code via the CELL TYPE 
PROGRAM, both parameters can also be selected manually, e.g. 
in case no predefined cell type program is available. For adding 
new cell type programs, please refer to chapter 2.7.4.

4.  Define control options for the selected vessel by choosing  

(figure 2.13, D)

5.  Optional: At this stage (or at step 7) you can save your defined 

experiment for future use by pressing the “SAVE” button. A keyboard 
will appear allowing you to define a name (max. length: 26 characters). 
You may enter further information about your experiment by touching 
the “Info” field and typing in your text (figure 2.13, E).

6.  Confirm and save the experiment parameters by pressing “OK” (saves 

the experiment and opens the drawer) or “SAVE” (saves the experiment 
for later use). 

7.  A summary of the defined settings will be displayed (figure 2.13, F). 

Please check for correctness before loading samples (see chapter 
2.9.2) and starting the experiments by pressing “START” (see chapter 
2.9.3)

A

D

C

F

E

B

Figure 2.13: 

Experiment definition (X Unit; example: 16-well  

Nucleocuvette™ Strips)

Figure 2.12: 

Vessel types for 4D-Nucleofector™ X Unit

2

Содержание 4D-Nucleofector

Страница 1: ...Bioscience Solutions 4D Nucleofector System Manual For Research Use Only...

Страница 2: ...System conveys to the buyer the non transferable right to use the system as well as Lonza s proprietary Nucleofector Technology for research conducted by the buyer whether the buyer is an academic or...

Страница 3: ...ofector Y Unit 18 2 10 1 Defining a New Experiment 18 2 10 2 Loading Samples 19 2 10 3 Running the Experiment 19 2 11 4D Nucleofector LV Unit 20 2 11 1 Using the 1 mL Nucleocuvette Cartridge Fixed Vol...

Страница 4: ...owing reliable transfection of adherent cells and cells in suspension Transfection of Any Substrate Nucleofector Technology offers high flexibility within applications since the same transfection para...

Страница 5: ...ioscience Solutions 5 The 4D Nucleofector System Support Teams Europe Scientific Support 32 87 321 611 scientific support eu lonza com North America Scientific Support 1 800 521 0390 toll free scienti...

Страница 6: ...power supply before cleaning and disinfecting the case Useadampclothtowipedowntheoutercasewithwateror70 80 ethanol Do not use any aerosols for cleaning Avoid wetting the cuvette holder within the cuv...

Страница 7: ...nit 1 mL or LV Nucleocuvette Cartridge for LV Unit 24 well Dipping Electrode Array forYUnit UsingconsumablesfromanyothersourcethanLonzawill preclude all warranty and liability claims Do not alter the...

Страница 8: ...mple rescue also see 3 2 using wheel accessible after removal of side panel via screw behind termination plug A typical 4D Nucleofector System includes 1 One 4D Nucleofector Core Unit 2 At least one f...

Страница 9: ...for completeness 2 Stack the units with the Core Unit containing the touch screen on top figure 2 4 3 Connect the units figure 2 5 by using the interface cables Connect the interface outlet port of t...

Страница 10: ...ector System Core Unit and functional units Figure 2 6 Main screen 2 7 2 Adjusting the Position of the Touch Screen The touch screen of the 4D Nucleofector System can be set at four angles 0 30 45 and...

Страница 11: ...onfirm selection or execute a program A Z Z A Top 10 Last 10 Sort a list alphabetically display the most frequent 10 items or the most recent 10 items Magnifier symbol Activate search functions i Disp...

Страница 12: ...s Load Samples chapter 2 9 2 10 or 2 11 Execute Nucleofection Experiment chapter 2 9 2 10 or 2 11 Prepare Samples According to Cell type Specific Optimized Protocol 2 8 General Instructions for Runnin...

Страница 13: ...ntaining cells and substrate The selected Nucleofection program will be applied to this position 2 No DNA Negative control Nucleofection program applied to vessel with cells but without substrate 3 No...

Страница 14: ...line of the list The experiment selected will be highlighted Confirm your selection by pressing OK 5 By pressing on the icons displaying the Nucleofection vessels or wells you can check the settings...

Страница 15: ...Z to find conditions more quickly a Select the desired cell type code by tapping on the appropriate line of the cell list The cell type selected will be highlighted For additional information about t...

Страница 16: ...leocuvette Strip theyellowpinattherearend of thestripmustbevisible figure2 14 C Ifthestripismounted inthewrongorientationitsrearendwillstayabovethestripholder and the yellow pin is hardly visible figu...

Страница 17: ...te s Proceed willbe displayed figure 2 15 C Load next samples and press YES to continue or press NO to interrupt the experiment 12 When the experiment is complete a result file summarizing the Nucleof...

Страница 18: ...line of the cell list The cell type selected will be highlighted For additional information about the cell type selected press i b To confirm your selection press OK c If required modify pulse code b...

Страница 19: ...the softwarewillcheckforusedwellsandofferyoudifferentoptionshow to continue 2 10 3 Running the Experiment 12 Afterloadingthesamplespress START toruntheexperiment figure 2 18 A 13 The progress of the...

Страница 20: ...part area 3 Injection port rear side 4 Air outlet port with 0 2 M sterile filter Components of the LV Nucleocuvette Cartridge figure 2 19 B C 1 Cartridge 2 Venting tube with 0 2 M sterile filter 3 Inl...

Страница 21: ...of defining solution and program code via the CELL TYPE PROGRAM both parameters can also be selected manually e g in casenopredefinedcelltypeprogramisavailable Foraddingnewcell type programs please r...

Страница 22: ...y a color code green for OK figure 2 22 C yellow in case of few errors and red in case of multiple errors figure 2 22 D If errors occurred you can check for more details by pressing More details There...

Страница 23: ...KIP and continue with step 14 4 Upon pressing YES the pinch valves will automatically open for 30 secondsallowingtoconvenientlyinsertthetubesintothethreepinch valves and a new window will appear figur...

Страница 24: ...o cell type specific protocol and mount it into a 4D Nucleofector LV Reservoir Rack figure 2 23 I 12 RemovetheredcapfromtheSpirosconnectorontheoutlettubeofthe cartridge and connect it to the swabbable...

Страница 25: ...apter 2 12 3 17 Optional At this stage or at step 20 you can save your defined experimentforfutureusebypressingthe SAVE button figure2 24 D Akeyboardwillappearallowingyoutodefineaname max length 26 ch...

Страница 26: ...pressing START H I Figure 2 25 Setup Checklist for LV Nucleocuvette Cartridge 1 Cartridge inserted in slot 2 Short venting tube with filter attached to the male Luer connector on the front plate 3 Tub...

Страница 27: ...rs figure 2 26 E and red in case of multiple errors figure 2 26 G If errors occurred you can check for more details by pressing More details The result details figure 2 26 F H will display the type of...

Страница 28: ...ttings list Firmware update update the system software see chapter 2 12 7for details Device cleaning opens the tray of the functional modules to remove it for cleaning see chapter 2 12 5 for details S...

Страница 29: ...he NEW field Edit existing programs by pressing EDIT or save your programs onto a USB stick by pressing SAVE figure 2 27 E To create a new custom program or to edit an existing program Press NEW or se...

Страница 30: ...D Nucleofector SystemwiththePCEditorsoftware seechapter2 13 Itisnecessaryto perform synchronization with each firmware update To start synchronization Insert a USB stick into the USB port on the front...

Страница 31: ...drive Insert 4D Nucleofector user information USB stick into the USB port of your PC Copy all files from the 4D Nucleofector PC Editor software folder to your hard disk preferably into a folder calle...

Страница 32: ...tion figure 2 29 B Select the USB stick and press SAVE Unplug the USB stick from your PC as soon as the experiment file has been saved NOTE Do not unplug the stick while saving Turn on the 4D Nucleofe...

Страница 33: ...easing DNA amount may lead to higher transfection efficiency but at the same time result in higher cell mortality Cell number in Nucleofection sample too high or too low Please use the cell numbers re...

Страница 34: ...irection of the red arrow as far as it will go figure 3 1 B Model variant B Newer Unplug system from main power Remove the terminator cap or cable connection to next unit figure 3 1 C Insert screw dri...

Страница 35: ...argecircumventingthesampleandis oftenaccompaniedbyaflashandanoise Thisproblemisusuallycaused by imperfect cuvettes or cuvette filling The 4D Nucleofector System is equipped with a hardware safety feat...

Страница 36: ...e of dipping electrodes that had been used before Err 22 Used well A weak pulse occurred Efficiency may be sub optimal Re used dipping electrode or inappropriate Nucleofector Solution Clear the error...

Страница 37: ...a for the Licensed Process and or the Purchased Device is complete Lonza does not warrant either that the use of the License does not infringe third parties rights or does not cause damages to third p...

Страница 38: ...n interfaces interface RS422 USB Lonza interface for module connection Shuttle HV Out X Unit only Spannungsbegrenzung voltage limitation limitation de tension 1500 V Strombegrenzung current limitation...

Страница 39: ...4D Nucleofector Manual Bioscience Solutions 39 6...

Страница 40: ...partyowners Theinformationcontainedhereinisbelievedtobecorrect and corresponds to the latest state of scientific and technical knowledge However nowarrantyismade eitherexpressedorimplied regarding it...

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