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09/07/ 24 (yy/mm/dd) Experimenter Kashima, Takashima, Hibino, Miyazawa Note-taker Takashima Title Flow Chart Sample Date Sample NameEnzymepurification KitProductStorage iGEM DNA parts kits 3-O-2 3-A-4 3-O-2 3-A-4 EcoR1 EcoR1, PST1 7/24 Miniprep Kit, Restriction Enzyme Digestion Electrophoresis 1.Miniprep Kit 2. Restriction Enzyme Digestion 3.Electrophoresis Restriction Enzyme Digestion 6F freezer
Miniprep Kit (Discussion) Cultured sample (090722 9:30 ～ 090723 16:50 ) ;3-O-2,3-A-4 Centrifuge 4 ℃, 15000 × g, 2min Remove the top of layer twice P1 250ul P2 250ul N3 350ul Centrifuge 4 ℃, 14000 × g, 10min Apply the top of layer to column Centrifuge RT, 10sec and remove through Buffer PB 500ul Centrifuge RT, 10sec and remove through Buffer PE 650ul Centrifuge 4 ℃, 17900 × g, 1min Exchange tube (remove C 2 H 5 OH) Milli Q 50ul RT 1min Centrifuge 4 ℃, 17900 × g, 1min Collect through and measure concentration
Result of Miniprep Kit (Discussion) Sample:conc. (ng/ul) 3-O-2283.5 3-A-4130.9
Description ( Electrophoresis ) (Discussion) Gel :Agarose Time : 12:50 ～ 13:20 Voltage: 100V 1234 Sample 3-O-23-A-43-O-23-A-4 3ul enzyme EcoR1 0.17ul 0.43ul enzyme H2OH2O1ul 1.4ul H buffer8.2ul 8.1ul Total12.7ul 12.9ul PST1 0.3ul 12345 samplename3-O-23-A-43-O-23-A-4Marker volume10 13 2.5 6×lodding buffer 222.6 0.5 37 ℃ incubate ( time: 090724 12:50 ～ 090724 13:20 )
Result of Electrophoresis (Discussion) This result indicates that the parts ( 3-O-2, 3-A-4) were treated with enzyme in appropriate way. 1000bp 5000bp １ 234M 3-O-23-A-4 parts length(bp)2837487 plasmid length(bp) 3266
09/07/ 17 (yy/mm/dd) Experimenter Kashima,Shihoya Note-taker Kashima Title Flow Chart Sample Date Sample NameEnzymepurification KitProductStorage 1.Miniprep.
Molecular cloning overview Steps to prepare vector hour overnight culture 2.Minipreps (day immediately following O/N) (use Qiaprep spin miniprep.
Restriction Digestion and Gel Electrophoresis Laboratory.
Miniprep 학기 기초유전학실험.
DNA Analysis Using Agarose Gel Electrophoresis Day 1
Mini-Prep Plasmid Isolation and Identification. Page 3-53 in lab manual & handout.
Lab safety Documentation, GLP Practical tips; primers and PCR.
DNA Restriction Analysis. 1. Obtain 4 tubes Use permanent marker to label B, E, H, C (on the lids) B = BamH1 E = EcoR1 H = Hind111 C= Control.
Abstract Little is known about the reproductive habits of paddlefish, a threatened species in Wisconsin and Minnesota. Biologists studying paddlefish spawning.
Week 7 Wednesday: –Screening of library transformants –Innoculation of colonies for plasmid preps –Practice PCR Turn in Lab #11 Thursday: –Plasmid minipreps.
Restriction Digest Laboratory Restriction fragment length polymorphism.
Plasmid mini prep DNA electrophoresis Transformation(Expression)
Gel Electrophoresis and Probes (Southern Blotting) Group A,
DEVELOPMENT OF A PCR BASED TEST TO DIFFERENTIATE PADDLEFISH AND STURGEON EGGS Scott Cooper, Jill Mader, Sue Kittleson, Valerie Hyde, Marc Rott Biology/Microbiology.
& Gel Plasmid Electrophoresis Mapping.
Separation of Proteins by Gel Electrophoresis Carolina Biological Kit #
Purification of DNA from a cell extract In addition to DNA, bacterial cell wall extract contain significant quantities of protein and RNA. A variety of.
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