Hi Jon,
Thank you for the reply. For the figure, we disconnected the amplifier and input the sine wave signal ( 10Hz, +/-0.5V) through the breakout box directly to test the DAQ card. The signal was added to only one channel (between the AI 0 and AI sense in breakout box 1) which should be channel 52 in NR screen. However, as you can see from the figure, all the left part of the NR screen show similar signal outputs. Is this because of settings or because of the open ends for the channels?
We didn't find the software or hardware settings for the signal mode (single referenced ended/differential/none refereneced signle ended). Is this single referenced ended mode a default setting for NR software?
Moreover, we tested the output of MEA neuron culture with whole system connected correctly according to the website. We put the amplifier in a incubator (37c, 20% humidity, 5% CO2). We powered the system using a DC power supply (+/- 6V) through the interface PCB.
For the gounding of the connections, we followered the MEA manual. We have two types of MEA (with/without internal reference electrode). For MEA with internal reference, we connected the channel (33 on NR screen) to MEA amplifier ground. For MEA without internal reference, we used an external Ag wire supplied by MCS to connect the MEA ground with culture media. What's the difference of the four goundings (1,8,57, and 64 on NR screen)? Is the additional ground when internal reference is used (33 on NR screen) different from these four goundings?
We still cannot obtain any signals even though we can see the neurons grow well on MEA using microscope. Do you think the current issue relevant?
Thank you.