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. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: J Histotechnol. 2020 Oct 1;43(4):163–173. doi: 10.1080/01478885.2020.1807228

Table 1.

Multiplex sequence order and control series


Primary Secondary Antibodies Negative Control Cross Over Control 1 Cross Over Control 2 Cross Over Control 3 Positive Control

1 anti-aSMA No (A) Yes Yes Yes Yes
anti-Mouse Yes No Yes Yes Yes (H)
2 anti-Vimentin No (B) No Yes Yes Yes
anti-Mouse Yes Yes (E) No Yes Yes (I)
3 anti-K19 No (C) N/A No Yes Yes
anti-Mouse Yes N/A Yes (F) No Yes (J)
4 anti-s100A4 No (D) N/A N/A No Yes
anti-Rabbit Yes N/A N/A Yes (G) Yes (K)

The final multiplex sequence is numbered and shows the application of primary and secondary antibodies for negative, crossover, and positive controls. Primary and secondary antibody pairs are highlighted. Each column corresponds to tissue section run through the entire multiplex labeling sequence (detection, scanning, elution and stripping performed between each antibody pair in sequence) unless otherwise specified (N/A). Yes: indicates reagent was applied. No: indicates antibody diluent substituted for primary antibodies. No: no secondary antibody reagent applied. Letters correspond to images shown in supplemental Figure 1.