Matt:LabNotes/2014-2-5: Difference between revisions
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>Mzcai (Created page with "===Quantifying Pre-circularized ppMALAT1=== *Alan did padlock probe capture in vitro AlanFung:LabNotes/Capturing/2014-1-23#Probe_calculations_ppMALAT1 '''Samples''' *5ul ...") |
>Mzcai |
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**Theoretically that mean it's more than the number of primary rolonies and even if we can only fix 1/10th of them that's enough for positive control | **Theoretically that mean it's more than the number of primary rolonies and even if we can only fix 1/10th of them that's enough for positive control | ||
*Need atleast 150ul so we can do 3 wells with positive control | *Need atleast 150ul so we can do 3 wells with positive control | ||
*Will do more reactions tomorrow: [[Matt:LabNotes/2014-2-6]] |
Revision as of 01:23, 7 February 2014
Quantifying Pre-circularized ppMALAT1
- Alan did padlock probe capture in vitro AlanFung:LabNotes/Capturing/2014-1-23#Probe_calculations_ppMALAT1
Samples
- 5ul of 10ng capture product: stored in 4C
- 9ul of 1000ng capture product: stored in -20C
- Positive control: 20ul of 2uM ppMALAT1 (linear ssDNA) = 40pmole x (92*303.7 + 79) pg/pmole = 1.12ug
- Negative control: 25ul of dsDNA PCR product from Noi (~1ug)
Procedure
Purify circular ssDNA with Zymo Kit
- Bring each sample to 60ul total with H2O
- Use Zymo ssDNA/RNA Clean & Concentrate Kit following default protocol
- Elute with 15ul H2O
Quantify with Qubit ssDNA Assay
- Buffer mix: 6ul reagent + 1194ul buffer = 1200ul
- Add 10ul of each standard control to 190ul buffer mix
- Add 1ul of each sample to 199ul buffer mix
Results
- 10ng capture product: too low to detect
- minimum detectable is 50pg/ul = 50ng/ml
- 1000ng capture product: 15.1ug/ml
- PosCtrl: 16.0ug/ml
- NegCtrl: too low to detect
Calculations
- PosCtrl: 16 ug/ml = 16 ng/ul
- 15ul * 16 ng/ul = 240ng
- 240ng/1.12ug = 21.4% yield
- 1000ng: 15.1 ug/ml = 15.1 ng/ul
- 15ul * 15.1 ng/ul = 226.5ng purified circular ssDNA
- Starting amount of ppMALAT1 used in capture reaction: 2ul * 1434 ng/ul = 2.868 ug (from Alan's notes)
- Fraction used for purification/quantification: 9/15 * 2.868 ug = 1.7208 ug
- 226.5ng/1.7208ug = 13.16% yield
- Maybe circular ssDNA has less yield during purification
- 226.5 ng * (nmole/28019.4ng) = 0.00808 nmole = 8.08 pmole
- 8.08 pmole/15 ul = 0.539 pmole/ul = 0.539 uM
- If none was used for PCR: 0.539 uM * 15/9 = 0.9uM
How much pre-circularized ppMALAT1 do we need for positive control?
- 1uM seems pretty reasonable considering that is about what we use for fluorescent-dye probes to detect primary rolonies
- Theoretically that mean it's more than the number of primary rolonies and even if we can only fix 1/10th of them that's enough for positive control
- Need atleast 150ul so we can do 3 wells with positive control
- Will do more reactions tomorrow: Matt:LabNotes/2014-2-6