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. 2010 Sep 30;1:37–42.

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This is an open access article, published under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/). This license permits non-commercial use, distribution and reproduction of the article, provided the original work is appropriately acknowledged with correct citation details.

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Figure 1. — 15% (w/v) SDS-PAGE gel of crude N. kaouthia venom, reconstituted (gel filtration fraction) NK-PLA₂: KTX-A complex, and purified venom proteins (KTX-A and KTX-B) under reduced (A) and non-reduced (B) conditions. A. Lane 1, molecular weight markers: phosphorylase b (97,400Da), bovine serum albumin (66,000 Da), ovalbumin (43,000Da), carbonic anhydrase (29,000Da), and lysozyme (14,300Da); Lane 2, reduced crude N. kaouthia venom (50μg); Lane 3, reduced fraction of reconstituted NK-PLA₂A: KTX-A complex (30μg); Lane 4, reduced fraction of reconstituted NK-PLA₂B: KTX-B complex (30μg); Lane 5, reduced NK-PLA₂ A (30μg); Lane 6, reduced NK-PLA₂ B (30μg); Lane 7, reduced KTX-A (30μg). B. Lane 1, non-reduced crude N. kaouthia venom (50μg); Lane 2, non-reduced KTX-A (10μg); Lane 3, non-reduced reconstituted NK-PLA₂ A:KTX-A complex (10μg); Lane 4, non-reduced NK-PLA₂ A (10μg).