Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Size Selection after fragmentation

    Hey there,

    This is my first post here - thanks for reading it!

    I'm rather lost. I'm prepping some samples for RNA-Seq, but in all four of my samples, I lose ~80-90% of my product at the mRNA fragmentation and cleanup step. I am using eukaryotic mRNA and am fragmenting with heat (94 C for 5 minutes) as per the protocol of the kit I'm using, which says these setting are ideal for fragmenting eukaryotic mRNA into 200 bp fragments.

    After fragmentation, I am doing a clean-up of the mRNA using 1.8X AmPure XP beads. Somewhere during these two steps I am dropping from ~ 5 ng/ul mRNA to 0.8 ng/ul fragmented mRNA, on average as demonstrated by BioAnalyzer, with some of my samples dropping to dangerously low levels (.2 ng/ul). The average size of my fragments is ~ 100-150 bp.

    Any idea why I'm losing so much product?

    My goal for the fragment size is 200 bp and I'd like to retain as much of it as possible (obviously). I'm thinking my next step should be to decrease the amount of time at 94 C to 4 minutes and to increase the concentration of AmPure to 2.4X, but I would greatly appreciate any feedback.

  • #2
    Most kits do not cleanup fragmented RNA and go straight to 1st strand synthesis which avoids any loss. I would not use such a kit. AMPure XP bead is not suitable for RNA and may result in RNA degradation. It meant to be used for DNA.

    Comment

    Latest Articles

    Collapse

    • seqadmin
      Essential Discoveries and Tools in Epitranscriptomics
      by seqadmin




      The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
      04-22-2024, 07:01 AM
    • 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

    ad_right_rmr

    Collapse

    News

    Collapse

    Topics Statistics Last Post
    Started by seqadmin, Yesterday, 08:47 AM
    0 responses
    12 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-11-2024, 12:08 PM
    0 responses
    60 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    59 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    54 views
    0 likes
    Last Post seqadmin  
    Working...
    X