BME103:Logistics
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| + | |style="background-color: #EEE"|[[Image:owwnotebook_icon.png|128px]]<span style="font-size:22px;"> BME 103 Fall 2012</span> | ||
| + | |style="background-color: #F2F2F2" | [[BME103 | <font face="trebuchet ms" style="color: #808080"> '''Home''' </font>]]<br>[[BME103:People | <font face="trebuchet ms" style="color: #808080"> '''People''' </font>]]<br>[[BME103:Projects | <font face="trebuchet ms" style="color: #808080"> '''Lab Write-Up 1''' </font>]]<br>[[BME103:Projects2 | <font face="trebuchet ms" style="color: #808080"> '''Lab Write-Up 2''' </font>]]<br>[[BME103:Projects3 | <font face="trebuchet ms" style="color: #808080"> '''Lab Write-Up 3''' </font>]]<br>[[BME103:Logistics | <font face="trebuchet ms" style="color: #808080"> ''' Course Logistics For Instructors''' </font>]] <br>[[BME103:Photos | <font face="trebuchet ms" style="color: #808080"> '''Photos''' </font>]] <br>[[BME103:WikiHelp | <font face="trebuchet ms" style="color: #808080"> '''Wiki Editing Help''' </font>]] | ||
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| + | | style="background-color: #ffcc66; padding: 5px;" colspan="2" | [[Image:BME494_Asu_logo.png]] | ||
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| + | <!-- ##### DO NOT edit above this line unless you know what you are doing. ##### --> | ||
| - | + | '''COURSE SPECS'''<br> | |
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| - | '''COURSE | + | |
* ~230 Freshmen | * ~230 Freshmen | ||
| - | + | ** 3 Lab sections, ~85 students per section | |
| + | *** 10 - 17 groups, of ~5 students per group | ||
| + | * 3 hours per class meeting | ||
| + | <br> | ||
| - | </ | + | '''TEMPLATE PAGES''' |
| + | * [[BME103:TEMPwu1 | Lab Write-up 1]] | ||
| + | * [[BME103:TEMPwu2 | Lab Write-up 2]] | ||
| + | <br> | ||
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| + | '''MATERIALS & METHODS - DNA AMPLIFICATION''' | ||
| + | * Reactions (100 μL total volume) contained: | ||
| + | ** Template DNA - Kozak ([http://partsregistry.org/wiki/index.php?title=Part:BBa_J176012 BBa_BBa_J176012]) inserted in plasmid vector V0120 ([http://partsregistry.org/wiki/index.php?title=Part:BBa_J176127 BBa_J176127]) via standard BioBrick ligation; ~10 ng per "positive" reaction; negative reactions contained no plasmid | ||
| + | ** Primers - Forward primer P0001 (5'-gggttttcccagtcacgacg), Reverse primer P0002 (5'-tgtggaattgtgagcggataaca). Amplicon size = 277 bp, spanning some of the vector, the BioBrick prefix sites, Kozak, the BioBrick suffix, and more vector sequence. | ||
| + | ** 2x GoTaq colorless PCR Master Mix - Promega M7133 | ||
| + | * A few of the samples were checked via standard ethidium bromide-stained agarose gel electrophoresis outside of class (see [http://openwetware.org/wiki/User:Karmella_Haynes/Notebook/ASU_courses/2012/10/24]). All other samples were measured via SYBRgreen staining on an LED fluorimeter. | ||
| + | * All reactions were run on an [http://openpcr.org/ Open PCR machine]. | ||
| + | <br> | ||
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| + | '''MATERIALS & METHODS - DNA IMAGING''' | ||
| + | * Details to be added soon | ||
| + | <br> | ||
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| + | '''OBTAINING MATERIALS''' | ||
| + | * We have written several worksheets and hand outs for this course. | ||
| + | * Please contact one of the instructors if you are interested in obtaining copies. | ||
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| + | |} | ||
Current revision
| Home People Lab Write-Up 1 Lab Write-Up 2 Lab Write-Up 3 Course Logistics For Instructors Photos Wiki Editing Help | |
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COURSE SPECS
TEMPLATE PAGES
MATERIALS & METHODS - DNA AMPLIFICATION
MATERIALS & METHODS - DNA IMAGING
OBTAINING MATERIALS
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