Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Need help interpreting these weird Bioanalyzer results

    Hi everybody,

    Today, I extracted RNA from plant material, which I want to - eventually - sequence. For quality check I ran them on the Bioanalyzer as I have done several times with the same type of samples and always had good results (high RIN, nice peaks, etc.) but this time it came out very weird... Lots of smear in some, in others almost nothing.
    I attached the whole output pdf, so maybe - please - someone here knows if this is my samples or the Chip or whatever?

    Thanks already! :-)
    Attached Files

  • #2
    Looks like RNA fragmentation or DNA contamination to me. The peaks are well correlated with the gel. If it was the chip, you'd have seen it across all samples. You might want to run an agarose gel yourself to confirm fragmentation. Maybe the DNAse treatment step was not very efficient? Or you didn't completely inactivate RNAse...
    Last edited by flobpf; 01-29-2014, 08:04 AM. Reason: grammar

    Comment


    • #3
      I didn't do DNA-free treatment yet. But I hadn't done before either when the results were good.
      I was suggested that the RNA hadn't completely resolved in the buffer. Can that be?

      Comment


      • #4
        Originally posted by Sciurus View Post
        I didn't do DNA-free treatment yet. But I hadn't done before either when the results were good.
        I was suggested that the RNA hadn't completely resolved in the buffer. Can that be?
        If that was the case, I think you'd see lighter bands and lower RNA yields. You wouldn't see new bands.

        Comment


        • #5
          Originally posted by flobpf View Post
          If that was the case, I think you'd see lighter bands and lower RNA yields. You wouldn't see new bands.
          Okay, thanks! So, you'd say it's DNA contamination?

          Comment


          • #6
            or RNA fragmentation due to incomplete inactivation of RNAse from sample.

            Comment

            Latest Articles

            Collapse

            • seqadmin
              Current Approaches to Protein Sequencing
              by seqadmin


              Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
              04-04-2024, 04:25 PM
            • seqadmin
              Strategies for Sequencing Challenging Samples
              by seqadmin


              Despite advancements in sequencing platforms and related sample preparation technologies, certain sample types continue to present significant challenges that can compromise sequencing results. Pedro Echave, Senior Manager of the Global Business Segment at Revvity, explained that the success of a sequencing experiment ultimately depends on the amount and integrity of the nucleic acid template (RNA or DNA) obtained from a sample. “The better the quality of the nucleic acid isolated...
              03-22-2024, 06:39 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by seqadmin, 04-11-2024, 12:08 PM
            0 responses
            25 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 10:19 PM
            0 responses
            27 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-10-2024, 09:21 AM
            0 responses
            24 views
            0 likes
            Last Post seqadmin  
            Started by seqadmin, 04-04-2024, 09:00 AM
            0 responses
            52 views
            0 likes
            Last Post seqadmin  
            Working...
            X