Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • sajoshi
    Member
    • Dec 2015
    • 26

    Bioanalyzer smallRNA results

    Please see attached bioanalyzer profile for a smallRNA chip. I ran the same samples twice, but the ladder is giving some problem. I prepared the gel two times separately thinking that the gel might have some problem. Can you provide your feedback as to why I am getting these results.

    I was planning to use these samples for Clontech smart ultra low input kit for RNA.

    Thanks
    Attached Files
  • nucacidhunter
    Jafar Jabbari
    • Jan 2013
    • 1250

    #2
    Interpreting results without a good ladder run is difficult. Some reasons could be following:
    1- Faulty reagents
    2- Dirty pin
    3- Other instrument issues

    Sample related issues:
    1- Presence of contaminants such as proteins and salts
    2- Residual gDNA
    3- Degraded sample

    I wonder why you run samples on Small RNA Chip. If you are going to prepare RNA-Seq library, they should be run on RNA Pico or Nano Chip depending on concentrations. You would need RIN from those Chips to decide on fragmentation time. Contacting tech support should resolve instrument or reagent related issues.

    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
    19 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-30-2026, 05:37 AM
    0 responses
    20 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 06-26-2026, 11:10 AM
    0 responses
    21 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...