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      "text": "Instrument is plagued by “a lot of false positives” and errors; required “a lot of energy and effort” only to fail; seems to work for simple antibodies but only about 70-80% of time; only worked 10-20% of the time for more complex ones.",
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      "text": "Machine seems to work for simple antibodies about 70-80% of time; only worked 10-20% of the time for more complex ones. “For the full-length antibodies, it will work fine; for the heavy chain-only antibodies, it probably worked on maybe two or three projects of the 20 or 30 that we ran...\"",
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      "text": "Instrument is plagued by “a lot of false positives” and errors; required “a lot of energy and effort” only to fail. “The sensitivity and the specificity of the binding... We did not see that level of specificity. We got a lot of false positives...\"",
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      "text": "“The sensitivity and the specificity of the binding, the nanomolar binding levels that you need to get the right candidate selection and eventually to get the right candidate antibody. We did not see that level of specificity. We got a lot of false positives that then you pull those cells out and clone them, and eventually try them on gels and stuff for detection of the target protein, and they would just not bind to them. So, there was something that was happening in the Berkeley Lights system that gave us false positives, and we would then spend a lot of energy and efforts to take these clones forward, but they would not pan out.” — Harbour Biomed ex-executive",
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      "text": "Source: Scorpion Capital consultation calls with experts",
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      "text": "HARBOUR BIOMED (cont'd): Instrument is plagued by “a lot of false positives” and errors; required “a lot of energy and effort” only to fail; seems to work for simple antibodies but only about 70-80% of time; only worked 10-20% of the time for more complex ones.",
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