Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • qPCR quantification of mRNA seq libraries: strange amplicon sizes

    We tried to do qPCR quantification of some Illumina paired-end mRNA seq libraries (+-325bp in length) using the following primers:

    qPCR primer 1.1 5’ AATGATACGGCGACCACCGAGAT 3’
    qPCR primer 2.1 5’ CAAGCAGAAGACGGCATACGA 3’

    The primers anneal to the 5'ends of the adapters and should thus amplify the entire fragment (the qPCR product size should be exactly the same as the original library product)

    After doing a serial dilution of a library (with known cluster numbers) we performed qPCR on a Roche LC480.
    We used several other libraries (with known sizes) as the unknowns. The standard curve generated was good with PCR efficiency of 93% and very low error. All of the amplifications looked good (Cp<15) and no template controls produced no product at all after 45 cycles.

    So on first impression, it seemed that the qPCR worked well - that is until we ran the products on agarose to see the product sizes. It turned out that the products were quite mixed but the prominent product which should have been the same size as the library turned out to be about 200bp larger than the library products.
    Pictures below show original library product and qPCR product (arrow). Other libraries (unmarked lanes) also feature the same pattern - product +-200bp larger than the library band.



    Any suggestions as to why the qPCR product was so much larger?
    Anyone out there doing routine qPCR quant of libraries - your input would be much appreciated!

  • #2
    I could not see your initial library on the gel, unlikely I know but running it alongside as a positive control might be helpful. Were all the other libraries the same 350bp size and did you run the PhiX as another control?

    It looks like you are using a SYBR based approach which will be confounded by the average insert size when trying to determine the number of molecules present as opposed to the amount of DNA. A TaqMan assay would be more reliable and I think this was proposed in the Quail et al publication.

    We are almost there on getting TaqMan QC ito our protocol, but it has been challenging to make it as robust as possible.

    Comment


    • #3
      thanks for your insight James,

      Library and qPCR product samples run on agarose side-by-side indicate the size difference as well.

      Unfortunately we do not have a phiX library to PCR as control. However, most of the libraries we used in the qPCR have been sequenced on the GA already.

      One question
      : Did you run your PCR products from your qPCR assay on a gel and get the same length as the library? Even when using a taqman assay, with PCR primers annealing to the ends of your library amplicons, you'd expect to amplify products of the same length as the library. If so, what primers have you been using? My primers are designed to anneal to the termini of the adapters.

      Any suggestions about how to go about the taqman assay would welcome.

      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
      28 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