User:Stuart McKellar/Notebook/Bird Sex Testing/2012/09/08: Difference between revisions
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During the addition of the first solutions (1a & 1b) I used the pipette tip to disturb the blood. This pulled some of the fibres out from the paper that the blood was on. I don't think that this should hurt the reaction. | During the addition of the first solutions (1a & 1b) I used the pipette tip to disturb the blood. This pulled some of the fibres out from the paper that the blood was on. I don't think that this should hurt the reaction. | ||
Primer prep: | |||
*2550F - 5´-GTTACTGATTCGTCTACGAGA-3´ | |||
32.5nm (0.21mg) | |||
Tm=51.2C | |||
Added 325ul water to make up a 100uM/L stock soln (Taken from http://www.protocol-online.org/biology-forums/posts/23706.html) | |||
He posted the following: | |||
When I get my primer which comes as lyophilized, I resuspend it to 100 uM/L concentration. For example, for an amount of 28.5 nM of lyophilized primer (the amount is provided by the vendor), I add 285 ul water or TE buffer and get 100 uM/L stock solution. To prepare 10 uM/L (or 10 pm/ul) working solution, I take 10 ul stock solution and add to 90 ul water. As you can see, no calculations are needed. | |||
-pcrman- | |||
*2718R - 5´-ATTGAAATGATCCAGTGCTTG-3´ | |||
32.6nm | |||
Tm=51.3C | |||
Added 326ul water | |||
Took 10ul of Primer and added to 90ul water to make a 10uM/L working solution. | |||
Revision as of 02:33, 8 September 2012
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Lab work for 8/9/2012
I am using 4 samples of the Diamond Doves, as they are being caught again in 4 weeks so it is OK if they don't work. Begin Lab workTransferred samples to 0.5mL tubes:
Carried out extraction according to protocol for tissue EDNA hispex kit. During the addition of the first solutions (1a & 1b) I used the pipette tip to disturb the blood. This pulled some of the fibres out from the paper that the blood was on. I don't think that this should hurt the reaction. Primer prep:
32.5nm (0.21mg) Tm=51.2C Added 325ul water to make up a 100uM/L stock soln (Taken from http://www.protocol-online.org/biology-forums/posts/23706.html) He posted the following: When I get my primer which comes as lyophilized, I resuspend it to 100 uM/L concentration. For example, for an amount of 28.5 nM of lyophilized primer (the amount is provided by the vendor), I add 285 ul water or TE buffer and get 100 uM/L stock solution. To prepare 10 uM/L (or 10 pm/ul) working solution, I take 10 ul stock solution and add to 90 ul water. As you can see, no calculations are needed. -pcrman-
32.6nm Tm=51.3C Added 326ul water Took 10ul of Primer and added to 90ul water to make a 10uM/L working solution.
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