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1674-pCold-GST-(3c)-NRF2
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== '''Cloning of 1674-pCold-GST-(3c)-NRF2''' == '''Purpose:''' Cloning of 1674-pCold-GST-(3c)-NRF2 '''Date: '''2013-2-14---2013-2-19 '''Notebook:0''' '''Page:''' '''Clone ID:1674''' '''Experimenters:''' yingying == '''Results''' == === subcloning === [[Image:1584+1674 clone 2-15-2013.JPG]]<br> subclone into 1629 pCold-GST-(3C) from 1661 pT7A3-MBP-(3c)-NRF2 using Nde1 + Xho1<br> <br> === Colony Screening === Date: 2013-2-18 Make miniprep and digest with Nde1 + Xho1 [[Image:1674 1611 2013 2 18 1.JPG]][[Image:1674 1611 2013 2 18 2.JPG]]<br> Only one clone, but it may be good.<br> [[Image:1657 clone 2-19-2013.JPG]]<br> the last lane is #1674 digest with Bgl11<br> == '''Result intepretation/Summary''' == == '''Conclusion''' == Not good. Forward primer has an extra G, will not express == == == '''Cloning of 1674-pCold-GST-(3c)-NRF2''' == '''Purpose:''' Redo Cloning of 1674-pCold-GST-(3c)-NRF2, previous cloning did not produce expression clone due to bad design of F primer. '''Date: '''2013-3-2---2013-3- '''Notebook:0''' '''Page:''' '''Clone ID:1674''' '''Experimenters:''' yingying == '''Results''' == PCR<br> {| cellspacing="1" cellpadding="1" border="1" |- | <br> |} === Colony Screening === Date: 2013-3-3 Make miniprep and digest with <br> 1. Nde1 + Xho1. [[Image:1661 1674 1683 Nde1 Xho1.jpg]]<br> 2. HindIII + Pst1<br> [[Image:1661 1674 1683 HindIII Pst1.JPG]] <br> <br> == Protein Expression == 2013/3/5<br> [[Image:1661 1674 1683 1676 3 6 2013.jpg]]<br> {| cellspacing="1" cellpadding="1" border="1" width="684" |- | Lane<br> | Name<br> | Clone ID<br> | Host<br> | Induction<br> | Purification<br> |- | M<br> | Fermentas PageRuler Plus<br> | <br> | <br> | <br> | <br> |- | 1<br> | pT7A3-MBP-(3c)-NRF2 <br> | 1661 clone 1<br> | 4 ml,<br> BL21(DE3)Star, pRare2-pLysS | 0.2 mM IPTG 25 oC o/n<br> | Ni beads<br> |- | 2<br> | pT7A3-MBP-(3c)-KEAP1<br> | 1661 Clone 2<br> | 4 ml, BL21(DE3)Star, pRare2-pLysS <br> | 0.2 mM IPTG 25 oC o/n<br> | Ni beads<br> |- | 3<br> | pCold-GST-(3c)-NRF2<br> | 1674<br> | 4 ml, BL21(DE3)Star, pRare2-pLysS <br> | 0.2 mM IPTG 25 oC o/n<br> | Ni beads (wrong, should use Glutathione agarose beads, no his tag)<br> |- | 4<br> | pCold-GST-(3c)-NRF2<br> | 1674<br> | 4 ml, BL21(DE3)Star, pRare2-pLysS <br> | 0.2 mM IPTG 25 oC o/n<br> | Ni beads (wrong, should use Glutathione agarose beads, no his tag)<br> |- | 5<br> | pCold-MBP-(3C)-NRF2<br> | 1683<br> | 4 ml, BL21(DE3)Star, pRare2-pLysS <br> | 0.2 mM IPTG 25 oC o/n<br> | Ni beads<br> |- | 6<br> | pCold-MBP-(3C)-NRF2<br> | 1683<br> | 4 ml,BL21(DE3)Star, pRare2-pLysS <br> | 0.2 mM IPTG 25 oC o/n<br> | Ni beads<br> |- | 7<br> | pT7A3-MBP-(3c)-KEAP1<br> | 1625<br> | 4 ml,BL21(DE3)Star, pRare2-pLysS <br> | 0.2 mM IPTG 25 oC o/n<br> | Ni beads<br> |- | 8<br> | pCold-MBP-(3C)-KEAP1<br> | 1676<br> | 4 ml,BL21(DE3)Star, pRare2-pLysS <br> | 0.2 mM IPTG 25 oC o/n<br> | Ni beads<br> |- | 9 | <br> | <br> | <br> | <br> | <br> |- | 10 | Purified MBP | <br> | <br> | <br> | <br> |} == == == protein expression result of NRF2 clones <br> == {| cellspacing="1" cellpadding="1" border="1" width="475" |- | clone ID<br> | expression<br> | gel reslut<br> | <br> |- | 1626, pET28-cold-NRF2<br> | no<br> | [[1625_1626_1656]]<br> | <br> |- | 1661,pT7A3-MBP-(3c)-NRF2<br> | yes,<br> | [[1661 1674 1683]]<br> | <br> |- | 1674,pCold-GST-(3c)-NRF2<br> | need to use GST beads<br> | [[1661 1674 1683]]<br> | <br> |- | 1683,pCold-MBP-(3C)-NRF2<br> | yes, <br> | [[1661 1674 1683]]<br> | <br> |- | 1698,pT7A3-NRF2<br> | no<br> | <br> | <br> |- | 1719,pT7A3-MBP-(E3C)-NRF2<br> | no<br> | [[626 1717 1719 1720]]<br> | <br> |- | 1748,pCold-8His-MBP-NRF2-6His<br> | only MBP<br> | [[1676 1726 1708 1748]]<br> | <br> |} <br> == '''Result intepretation/Summary''' == == '''Conclusion''' == [[Category:Cloning]]
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