Blue:RNA-Seq Experiments:11212016

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Revision as of 22:55, 21 November 2016 by >B1lake (Created page with "==Kidney Samples: Nuclei isolation for Drop-seq== *Samples from Andy Ransick (McMahon lab, USC) gently frozen in 1ml cryopreservative: #8x Dissected nephrons **Thawed and add...")
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Kidney Samples: Nuclei isolation for Drop-seq

  • Samples from Andy Ransick (McMahon lab, USC) gently frozen in 1ml cryopreservative:
  1. 8x Dissected nephrons
    • Thawed and added 1ml isce cold PBS
    • Centrifuged at 300g for 5min
    • removed most of the media and added 1ml of NEB
    • Incubated on ice 10min and continued with dounce (5x loose pestle, 10x tight pestle)
    • Very low count - repeated dounce tight pestle 10x - still very low count
    • Centrifuged and FACS - only 7200 nuclei total sorted
    • Centrifuged and resuspended in 10 ul - only 80/ul final -> too low to run on Drop-seq or C1 -> froze down as potential bulk control
  • Samples from Sanjay Jain's lab (Washington University):
  1. Adult kidney tissue K1600543_1 (fresh frozen)
    • Removed from -80C to ice, chopped using scalpel on ice (petri dish)
    • Transfered to NEB in dounce on ice
    • 5 strokes with loose pestle -> ice 10 min
    • 15 strokes with tight pestle -> removed super (Filtered 50um filter) and left undissociated tissue (~3M nuclei)
    • Added another 1ml NEB to undissociated tissue -> 15 strokes with tight pestle -> removed super (Filtered 50um filter) and left undissociated tissue (~650K nuclei)
    • Centrifuged and combined all nuclei - re-filtered (30um filter) before FACS -> 2x 200K for DROP-seq
    • Froze down remaining unsorted nuclei as potential bulk control