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. 2016 Mar 17;18:9. doi: 10.1186/s12575-016-0038-x

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© Bhosle et al. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 2 — OAS1 protein expression in crude and purified lysates of prostate cancer cell line. OAS1 p46 isoform expression in lysates from 293T, RwPE1, DU145 and LNCaP cell line. a OAS 1 expression in 20 μg crude lysates (upper panel) and GAPDH (lower panel) was used as a loading control. b OAS 1 expression in lysates purified from 20 μg of crude lysates with activated poly I:C bound sepharose beads (upper panel), GAPDH (middle panel) was used as a loading control and elute-1 collected during washing to remove the unbound OAS enzyme and OAS free cell lysates. DU145 lysates purified with unactivated sepharose beads with no poly I:C bound to it was used as a negative control