Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • bunnymac
    Junior Member
    • Sep 2010
    • 2

    Dynabeads mRNA isolation problem

    I have a problem to isolate mRNA with Dynabeads.

    I extracted total RNA from Chlamydomonas with AMBION RiboPure kit.

    After that, I purified the total RNAs with Qiagen RNeasy mini kit.

    And I used Dynabeads to isolate mRNAs but it showed strange picture.

    Its picture is attached.

    When I tried to make libraries with these samples, I failed. (No bands)

    I checked the total RNAs quality by Bioanalyzer 2100 and they are good.

    Does anybody have some idea about this problem?

    Thanks in advance,

    JJ
    Attached Files
  • epistatic
    Senior Member
    • Mar 2009
    • 129

    #2
    Did you measure your cDNA yield after mRNA capture, frag, and 1st/2nd strand? We like to do that QC step before taking samples through library process. It could also be helpful to run the enriched mRNA on the bioanalyzer. From the picture and failed libraries it would be hard to say what the problem was.

    Comment

    • bunnymac
      Junior Member
      • Sep 2010
      • 2

      #3
      Bioanalyzer-mRNA

      I checked the mRNA level with bioanalyzer.
      But I could not get any mRNA with Dynabeads.
      Attached Files

      Comment

      • gogreen
        Member
        • Apr 2009
        • 18

        #4
        hi bunnymac,
        Probably you've figured out the issue already, but I just saw the bioanalyzer profile now and realized that it was a RNA Nano. When you say 4/6/8 ug, do you mean total RNA or mRNA? (I hope it's the first one!) Did you measure the amount of mRNA before running a bioanalyzer?. The RNA Nanos are not quite sensitive for things less than 10 ng which could be the case here (since you do see some faint signal in the last samples). I would try running them on a RNA Pico chip. I use Seramag beads for mRNA purification and with 10 ug of Total RNA, I normally see the mRNA.
        Cheers!

        Comment

        • EMONGS
          Junior Member
          • May 2011
          • 4

          #5
          I agree with go green...and just to add, it is not unusual to not see bands even if the concentration is high. I would start over with more sample; if possible use an invitrogen magnetic rack and just cut the library where you need to after ligation and proceed from there.

          All the best!

          Comment

          • gogreen
            Member
            • Apr 2009
            • 18

            #6
            hi Emongs, IMHO, the invitrogen magnet doesn't work any better than other ones. I totally quit using invitrogen magnets and now use magnets which costs nothing compared to the terribly expensive invitrogen ones. Even fridge magnets would actually work

            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
            16 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-30-2026, 05:37 AM
            0 responses
            17 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-26-2026, 11:10 AM
            0 responses
            20 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 06-17-2026, 06:09 AM
            0 responses
            54 views
            0 reactions
            Last Post SEQadmin2  
            Working...