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. Author manuscript; available in PMC: 2021 Apr 7.
Published in final edited form as: Anal Chem. 2020 Mar 24;92(7):5311–5318. doi: 10.1021/acs.analchem.9b05853

Figure 2.

Figure 2.

Layout of the consumable for 6 samples in which the following steps occur. (1) Lysis and homogenization occur in lysis tubes, which include a magnetized stir disc and glass beads. (2) The TruTip aspirates the sample mixed with a binding buffer so that it flows through the pores of the matrix in the tip resulting in DNA bound to the matrix. (3) The porous matrix is washed to remove the impurities. (4) The matrix is dried with air. (5) The bound DNA is eluted into an elution buffer. (6) The purified DNA is amplified with an asymmetric PCR reaction. (7) The product (with fluorescent labels) hybridize to the gel elements. (8) The gel elements are washed to remove unbound product. And, (9) an image of the array is captured and analyzed.