Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • mateo
    Junior Member
    • May 2010
    • 2

    tRNA/5S rRNA depletion

    Dear all,
    I'd like to deplete tRNA and 5S rRNA from total RNA to clone and deep sequence primarily precursor miRNAs in eukaryotic cells. I'm assuming that pre-miRNA are at a very low concentration when compared to tRNA/5S so if these species are left in my sample preparation they will represent the vast majority of sequences. Any help and/or suggestions would greatly be appreciated.
    Thanks.
  • whw
    Member
    • Jun 2011
    • 19

    #2
    Gel purification can be a good way of eliminating larger species. I know that Bioo Scientific includes a gel purification step in their small RNA sequencing protocol.

    Comment

    • pmiguel
      Senior Member
      • Aug 2008
      • 2328

      #3
      Originally posted by mateo View Post
      Dear all,
      I'd like to deplete tRNA and 5S rRNA from total RNA to clone and deep sequence primarily precursor miRNAs in eukaryotic cells. I'm assuming that pre-miRNA are at a very low concentration when compared to tRNA/5S so if these species are left in my sample preparation they will represent the vast majority of sequences. Any help and/or suggestions would greatly be appreciated.
      Thanks.
      Epicentre RiboZero Gold?

      --
      Phillip

      Comment

      • protist
        Senior Member
        • Jan 2009
        • 101

        #4
        Originally posted by pmiguel View Post
        Epicentre RiboZero Gold?

        --
        Phillip
        RiboZero Gold will not remove tRNA, its advantage is it will remove mitochondrial as well nuclear encoded rRNA. To my knowledge aside from size selection of below tRNA size (~70 nt) there is not an effective kit out there..

        Comment

        • mnkyboy
          Member
          • Mar 2009
          • 87

          #5
          You can see the tRNA pretty well in a gel. I would try the RZ beads to clean it up then gel purify.

          Also it will probably be easier to purify out after library preparation than as RNA by gel.

          Comment

          Latest Articles

          Collapse

          • SEQadmin2
            Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
            by SEQadmin2



            Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
            ...
            07-09-2026, 11:10 AM
          • SEQadmin2
            Cancer Drug Resistance: The Lingering Barrier to Rising Survival
            by SEQadmin2



            Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

            There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
            07-08-2026, 05:17 AM
          • GATTACAT
            Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
            by GATTACAT
            Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
            07-01-2026, 11:43 AM

          ad_right_rmr

          Collapse

          News

          Collapse

          Topics Statistics Last Post
          Started by SEQadmin2, 07-13-2026, 10:26 AM
          0 responses
          25 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-09-2026, 10:04 AM
          0 responses
          35 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-08-2026, 10:08 AM
          0 responses
          22 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 07-07-2026, 11:05 AM
          0 responses
          34 views
          0 reactions
          Last Post SEQadmin2  
          Working...