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I work in an enzymology lab focusing towards protein crystallography. We express our gene in pET-28(a) expression vector inside E.coli BL-21(DE3) host leading to protein expression. The problems...
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I am having a trouble while trying to dissolve two compounds, one is Ebselen and another is Zofenopril calcium. I am trying primarily with DMSO. Ebselen is dissolving in 100uL DMSO but problem...
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I have got 4-5 extra bands in SDS gel after running a my eluted protein which was purified through Ni-NTA column. This means impurities are present. My question is, can I again run my protein...
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