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1 KB (162 words) - 16:57, 8 June 2020
- # Tail digest DNA *[[PCR Amplification of DNA]]773 bytes (111 words) - 17:00, 8 June 2020
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1 KB (161 words) - 17:58, 5 June 2009
- #Resuspend DNA in 6 mL of distilled water. Add 10g of CsCl and dissolve.1 KB (167 words) - 22:03, 17 January 2012
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1 KB (179 words) - 21:24, 3 November 2009
- [[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
- # Select '''Enter Individual DNA Sequencing Requests''' * 1 uL of template (unless the plasmid DNA concentration is >500 ng/uL in which case dilute it to 50-300 ng/uL646 bytes (108 words) - 18:34, 5 March 2014
- This protocol is for extracting DNA from TRIZOL preparations after the RNA-containing upper phase has been comp ...sion or use the shaker. '''NEVER''' vortex samples, as it will destroy the DNA.3 KB (417 words) - 17:42, 25 September 2015
- ===DNA Extraction=== ** 1 uL of the Extracted DNA from the previous step.2 KB (262 words) - 20:02, 13 July 2015
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6 KB (867 words) - 19:50, 13 September 2019
Page text matches
- *[[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 tapping598 bytes (104 words) - 15:44, 12 February 2014
- #Add 1 uL T4 DNA Ligase (Invitrogen). ##Add DNA and mix gently1 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 final1 KB (236 words) - 18:45, 17 February 2010
- #Paste dna sequence in top box427 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 Ladder2 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) * 2.51 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 Opt1 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-DNA2 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 a6 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