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  • *[[PCR Amplification of DNA]] *[[Cesium Chloride Preparation of DNA]]
    4 KB (484 words) - 12:10, 15 August 2016
  • *DNA of interest (1 uL for plasmid, 5 uL for cloning/mutagenesis) #Add DNA to cells and mix by tapping
    598 bytes (104 words) - 15:44, 12 February 2014
  • #Add 1 uL T4 DNA Ligase (Invitrogen). ##Add DNA and mix gently
    1 KB (227 words) - 14:40, 7 May 2009
  • # Tail digest DNA *[[PCR Amplification of DNA]]
    773 bytes (111 words) - 17:00, 8 June 2020
  • *DNA: CsCl Purified or siRNA (resuspended to 0.1 nmol/uL with 200 uL water) #500 uL of cells is mixed with 50-200 ug of DNA (or 5 uL siRNA) in a 0.4 cm cuvette. These volumes are for half of a final
    1 KB (236 words) - 18:45, 17 February 2010
  • #Paste dna sequence in top box
    427 bytes (73 words) - 13:24, 27 May 2009
  • #Resuspend DNA in 6 mL of distilled water. Add 10g of CsCl and dissolve.
    1 KB (167 words) - 22:03, 17 January 2012
  • * DNA - typically transfect 50-1000 ng DNA per well ##Per ug of DNA need 3 uL Fugene.
    1 KB (198 words) - 13:22, 29 August 2011
  • *OptiMEM(in uL, equal for DNA and Lipofectamine) = Lipofectamine(in uL) * 50 ##Combine the two volumes of OptiMEM/DNA and OptiMEM/Lipofectamine (should be 200uL/well).
    1 KB (148 words) - 16:39, 18 December 2009
  • *Load 1 and 3 uL of diluted RNA, plus 4 or 8 uL of 1 kB Plus DNA Ladder
    2 KB (290 words) - 14:31, 1 October 2009
  • *Herring testes DNA (Clontech Cat# 17401336) #Boil hering tested DNA for 5 min at 95C then cool on ice.
    2 KB (292 words) - 17:14, 22 December 2009
  • *Calculate DNA to transfect *Lipofectamine(in uL) = DNA(in ug) * 2.5
    1 KB (155 words) - 21:00, 11 July 2012
  • *GST-HA-S6K1 plasmid. Prepare by [[Cesium Chloride Preparation of DNA]]. Need 500 ug per 10 plates of cells #Combine 500 ug DNA with 10 mL OptiMEM, and separately 700 uL Lipofectamine 2000 with 10 mL Opt
    1 KB (185 words) - 19:59, 20 September 2012
  • *Herring testes carrier DNA. Boil 20min then place on ice before use #Place Herring DNA on heating block at 95C for 20min then immediately on ice before use.
    2 KB (274 words) - 15:02, 14 December 2009
  • Order primers through IDT-DNA
    2 KB (353 words) - 19:47, 13 December 2010
  • ===Linearization and Purification of Shuttle DNA=== #Digest 0.2-0.5 ug plasmid DNA in 100 uL volume with 30-100U of PmeI overnight at 37C. If desired check a
    6 KB (872 words) - 20:56, 11 July 2012
  • [[ Category:DNA]]
    2 KB (297 words) - 14:32, 23 July 2021
  • [[Category: DNA]]
    1 KB (184 words) - 15:20, 21 May 2018
  • [[Category:DNA]] ===Yeast DNA Prep Buffer===
    1 KB (197 words) - 16:32, 21 February 2012
  • [[Category:DNA]] ...Yeast. See [[Rapid Isolation of Genomic DNA from Yeast]]. Use 1µl of the DNA in your PCR reaction.
    1 KB (248 words) - 16:39, 21 February 2012

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