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. Author manuscript; available in PMC: 2018 Apr 18.
Published in final edited form as: Methods Mol Biol. 2017;1639:195ā€“209. doi: 10.1007/978-1-4939-7163-3_19

Fig. 2.

Fig. 2

Step 1 of the AAT protein purification process. FPLC chromatogram of AAT in the supernatant (labeled ā€œLā€) eluted from the Q Sepharose Fast Flow column using (a) a continuous linear salt gradient method, or (b) a 3-step gradient method. SDS-PAGE of fractions eluted from column 1 in (b) is shown in panel (c). The fractions within peak 1 contain AAT. The dashed line shows the salt gradient used for elution. The labels, T and UB, denote the total cell lysate and flow through fraction from the column respectively