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  • 實驗方法> RNA實驗技術> RNAi>The pSico and pSicoR Design and Cloning

    The pSico and pSicoR Design and Cloning

    關鍵詞: 來源: 互聯網

    pSico Oligo Design

    Click on the Mac OSX program pSicoOligomaker 1.5 to select and design oligos for pSico and plentilox3.7.

    To operate it, simply paste your sequence in the "sequence" window, give it a name (optional), select a cutoff value (from -2 to 9) and click "search". The program will list in the right window all the potential 19-mers with a score equal or higher than the cutoff. The score is given based on a set of criteria published in Nature Biotech. by Reynolds et al. in 2004. According to the authors, a 19-mer with a value higher than 6 has approximately 90% chance of achieving silencing of the target mRNA.

    You can select all targets and paste them in Word or Excel to store the result. In addition, if you type or paste a 19-mer in the field "target" and click on "make oligos" the program returns the sequence of the forward and reverse oligos (both in the 5' to 3' orientation) that have to be ordered to clone in pSico. The button "order" directs you to the web page we use to order oligos. The button "settings" lets you change the criteria to design the oligos (loop sequence and length, overhangs, etc) so that it can be used to design oligos for other vectors.

    "Clear sequence" tells the program to remove all illicit characters, including spaces and "end of line", from the sequence. In addition, it converts the sequence to all caps.

    In case you don't have a Mac, or you prefer to design your oligos manually, here is an example:

    19mer: GTAGCTTAGCGTCGGAGCT

    sense oligo:

    5'-TGTAGCTTAGCGTCGGAGCT-TTCAAGAGA-AGCTCCGACGCTAAGCTACTTTTTTC

    antisense oligo:

    5'-TCGAGAAAAAAGTAGCTTAGCGTCGGAGCT-TCTCTTGAA-AGCTCCGACGCTAAGCTACA

    How to clone into pSico and pSicoR:

    We order 5’ phosphorylated, PAGE purified oligos designed using the program PSICOLIGOMAKER 1.5.

    Oligos are resuspended in distilled water to a final concentration of 100μM.

    Oligos annealing:

    Mix:

    -- ddH2O 23μl

    -- sense oligo 1μl

    -- antisense oligo 1μl

    -- 2X Annealing Buffer 25μl (recipe see below)

    ? Incubate 4 minutes at 95?C

    ? Incubate 10 minutes at 70?C

    ? Slowly cool down the annealed oligos to 4?C (Store at ?20?C)

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