Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • d00b9p
    Junior Member
    • May 2013
    • 2

    #1

    Genomic DNA QC using Bioanalyzer?

    This might sound like a daft question, but if I was to run 1 ul of genomic DNA on a Bioanalyzer HS chip would I be able to detect sample degradation? I realise that high molecular weight genomic DNA will be far too large to be detected, but would any smaller weight 'smear' show up on the Bioanalyzer trace?

    We have some insect extractions with very little DNA (~100 ng) from a whole insect. We have found running out the DNA on a gel to be quite a poor way of seeing the DNA quality - needing at least 30 ng and using Ethidium staining. While we can sometimes see the faint high molecular weight band, it is near impossible to see if there is much 'smear'. And the main problem is that we have so little DNA in the first place.

    I wondered if using the Bioanalyzer may help, since it uses so little of the precious sample.
  • chevrm
    Member
    • Apr 2012
    • 14

    #2
    I'd consider a 12000 chip if you're willing to burn 1uL...it should be able to visualize anything over 0.5ng/uL

    Comment

    • Susanne
      Member
      • Aug 2009
      • 33

      #3
      The HS chip is quite sensitive with regards to genomic DNA and overloading. So I would recommend not to load more than 50 ng/µl, better around 10-15 ng/µl if you want to quantify. There are several problematic aspects to it though - if your sample runs into the upper marker, your quantification will be biased, and if you load too much, the quantification will also be wrong.
      Genomic DNA cannot enter the channels and it's possible that the chip doesn't run properly (if the gDNA is not degraded).
      The 0.5 ng/µl quoted for the 12000 chip is referring to this concentration in a single peak. You will not see this concentration in a smear sample (more like 5 ng/µl required).

      Comment

      Latest Articles

      Collapse

      • SEQadmin2
        Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
        by SEQadmin2



        CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

        Despite this, “CRISPR helped turn genome editing from a specialized technique into
        ...
        07-31-2026, 11:01 AM
      • SEQadmin2
        Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
        by SEQadmin2


        Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

        The systematic characterization of the human proteome has
        ...
        07-20-2026, 11:48 AM
      • 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

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, Yesterday, 10:13 AM
      0 responses
      14 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-31-2026, 02:55 AM
      0 responses
      28 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-24-2026, 12:17 PM
      0 responses
      21 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 07-23-2026, 11:41 AM
      0 responses
      20 views
      0 reactions
      Last Post SEQadmin2  
      Working...