User:Karmella Haynes/Notebook/BioBrick cloning/2013/09/06: Difference between revisions

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'''DNA Concentration Data'''
<!-- Wiki code notes: The {| is the opening tag for tables. {{table}} is an OWW template that creates thin grey border lines and cell margins.
<!-- Each |- starts a new row. There are three rows. bgcolor=#cfcfcf *colors* the *background* of the first row grey.  -->
<!-- Below that, each | starts a row of cells. -->
<!-- The symbol || separates cells in a row. Replace the --- in each cell with your data. -->
<!-- If you have only one plasmid, delete the |- under Plasmid 1's row, and delete the entire row for Plasmid 2.-->
<!-- |} must be the last symbol (on its own line) in the table. This is the table closing tag. -->
{| {{table}}
|- bgcolor=#cfcfcf
| Plasmid || OD260 || OD260/280 || ng/μL
|-
| 1. Plasmid 1 || 0.108 || 1.841 || 108.321
|-
| 2. Plasmid 2 || 0.007 || 1.75 || 6.60
|}
* Streak #2 did not grow well. Culture might be empty bacteria. Use mini prep 1 for other steps.
'''Restriction Digest Table'''<br>
* Checked plasmid minipreps with EcoRI/PstI digests
{| {{table}} border="1" cellspacing="3"
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<!-- bgcolor=#cfcfcf *colors* the *background* of the Reagent and Volume cells grey.  -->
<!-- The next two "rowspan=7" cells span  all 7 rows in the table so that they can fit the "Expected" list and a gel image. rowspan is how you create merged rows in Wiki code. -->
<!-- Replace Plasmid 1 and 2 with the names of your plasmids. Replace insert size and vector size with appropriate information for your plasmids. If you only have one Plasmid, delete all the text for Plasmid 2
<!-- After you upload your gel image to OWW, replace "GelImage.jpg" with the name of your image file -->
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|- valign="top"
| bgcolor=#cfcfcf | Reagent
| bgcolor=#cfcfcf | Volume
| rowspan="7" | <u>Expected:</u><br>1. CMV colony 1 = 588, 3200<br>2. CMV colony 2 = 588, 3200<br>3. CMV control = 588, 3200<br>
| rowspan="7" | [[Image:GelImage.jpg|400px|Today's gel]]<br>15 μL/lane; 1% agarose; [http://openwetware.org/wiki/Image:KAH_Fermentas_GeneRuler_1kbplus.jpg Ladder]
|-
| DNA(plasmid) || 3.0 μL
|-
| 10X buffer || 1.5
|-
| EcoRI || 1.0
|-
| PstI || 1.0
|-
| dH<sub>2</sub>O || 8.5
|-
| &nbsp; || 15 μL --> 37°C/ 15 min.
|}
'''DNA Sequencing Samples'''
<!-- * signs create an automatically bulleted list. Replace 'date' with the date you submitted the samples -->
* Submitted to DNASU on 'date'
<!-- # signs create an automatically numbered list. Replace Plasmid 1 & 2 with the names of your plasmids. Replace 'name' with the appropriate name of each primer. -->
# Plasmid 1 - forward primer 'name'
# Plasmid 1 - reverse primer 'name'
# Plasmid 2 - forward primer 'name'
# Plasmid 2 - reverse primer 'name'





Revision as of 19:25, 6 September 2013

Karmella's BioBrick Cloning <html><img src="/images/9/94/Report.png" border="0" /></html> Main project page
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09/06/13

  • Miniprep - CMV
  • Restriction digest - CMV
  • Sequencing - CMV [cloning bootcamp demo]



Results

  • CMV/V0120
    • Culture innoculated on 9/05/13
    • Results for liquid cultures: (1) grew, (2) grew
    • Results for streak plate: (1) grew well, (2) hardly any growth


List of Samples for Minprep & Analysis

  1. Sample 1 = CMV/V0120 colony 1; BBa_J176027; part = 588 bp; vector = 3200
  2. Sample 2 = CMV/V0120 colony 2; same
  3. Sample 3 = CMV/V0120 (control DNA); BBa_J176027; part = 588 bp; vector = 3200


DNA Concentration Data

Plasmid OD260 OD260/280 ng/μL
1. Plasmid 1 0.108 1.841 108.321
2. Plasmid 2 0.007 1.75 6.60
  • Streak #2 did not grow well. Culture might be empty bacteria. Use mini prep 1 for other steps.


Restriction Digest Table

  • Checked plasmid minipreps with EcoRI/PstI digests
Reagent Volume Expected:
1. CMV colony 1 = 588, 3200
2. CMV colony 2 = 588, 3200
3. CMV control = 588, 3200
Today's gel
15 μL/lane; 1% agarose; Ladder
DNA(plasmid) 3.0 μL
10X buffer 1.5
EcoRI 1.0
PstI 1.0
dH2O 8.5
  15 μL --> 37°C/ 15 min.


DNA Sequencing Samples

  • Submitted to DNASU on 'date'
  1. Plasmid 1 - forward primer 'name'
  2. Plasmid 1 - reverse primer 'name'
  3. Plasmid 2 - forward primer 'name'
  4. Plasmid 2 - reverse primer 'name'