Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • luc
    Senior Member
    • Dec 2010
    • 469

    Substitute for Ribozero beads?

    Has anybody had success in substituting the ribozero magnetic beads (which are the limiting reagent in the kits)?
    They are very likely simple streptavidin coated beads; but how much of the substitute will be required?

    Thanks in advance!
  • nucacidhunter
    Jafar Jabbari
    • Jan 2013
    • 1250

    #2
    I do not have direct experience with your query. Beads have a binding capacity that can be found in manufacturer specification sheet and quantity or number of transcripts that are depleted can be estimated. Using twice the estimated amount is a good starting point.

    On the subject of rRNA depletion there are other products which are more cost effective:

    1- Lexogen RiboCop (works by hybridisation of RNA to probes and binding probes to beads similar to Ribo-Zero Gold)
    2- RNaseH based degradation product from NEB
    3- Clontech SMARTer products with kit included RiboGone (RNaseH based) reagent. These products have a considerable time-saving advantage as well because they have ligation-free workflow
    4- Post-cDNA synthesis depletion workflows
    Last edited by nucacidhunter; 12-11-2015, 02:28 AM.

    Comment

    • luc
      Senior Member
      • Dec 2010
      • 469

      #3
      Thanks!

      for plant RNAs the choices are fewer, though. I am looking to substitute the beads for another lab that has lost the part of the kit (the beads) but still has the reagents that were stored in the freezer.

      This protocol (http://www.jove.com/video/50093/depl...enomic-rna-seq) uses NEB streptavidin beads and should be pretty easy to follow (I am not generating our own baits for the moment).

      Comment

      • nucacidhunter
        Jafar Jabbari
        • Jan 2013
        • 1250

        #4
        The issue would be the unknown buffer composition of the beads. They might have adjusted salt concentration to make it compatible with rRNA Binding Buffer carried over to beads. If the buffer is not right then it might affect binding and result in carry over of rRNA to next step. This applies to Ribo-Zero plant that comes with TruSeq stranded total RNA-Seq kit. The workflow for epicentre or stand-alone Ribo-Zero is different but the composition of Magnetic Bead Resuspension Solution still is unknown.

        Edit: for plants other option is NuGEN Ovation kits that uses In-DAC technology and they can design custom probes but I am not sure if hey charge more for custom probes. They mention that design is free.
        Last edited by nucacidhunter; 12-11-2015, 03:05 AM.

        Comment

        Latest Articles

        Collapse

        • 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
        • SEQadmin2
          Nine Things a Sample Prep Scientist Thinks About Before Sequencing
          by SEQadmin2


          I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

          Here are nine questions we think about, in roughly the order they matter, before...
          06-18-2026, 07:11 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, 07-02-2026, 11:08 AM
        0 responses
        22 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-30-2026, 05:37 AM
        0 responses
        23 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-26-2026, 11:10 AM
        0 responses
        22 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 06-17-2026, 06:09 AM
        0 responses
        55 views
        0 reactions
        Last Post SEQadmin2  
        Working...