Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Urgent - MiSeq 12.5pM PhiX concentration

    If I use the MiSeq v3 kits, according to the denature & dilute guide (attached), I dilute both my PhiX and library concentration to the same concentration, and spike in the desired Phix percentage. For example, if I want to load 15pM at 25% PhiX, I denature and dilute both Phix and library to 15pM, then 150uL of 15pM PhiX + 450uL of 15pM library.

    If I use MiSeq v2 kits, the guide says to dilute PhiX to 12.5pM. If I wanted to load the same 15pM at 25% PhiX, what is the calculation? Am I having PhiX at 12.5pM and the library at 15pM dilution? How to do this for v2 kits?
    Attached Files

  • #2
    if you have 1000ul of library at 15pM, you should have 15000pmol of material. 25% of that should be 3750pmol (that'll be your PhiX target). There are three ways to proceed:
    From the 20pM denatured stock, use 187.5ul. (187.5 * 20 =3750)
    From the 15pM denatured/diluted PhiX, use 250ul (250 * 15 = 3750)
    From 12.5pM denatured/diluted PhiX, use 300ul. (300 * 12.5 = 3750)

    That should get you close to the desired spike-in, I think.

    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...
      Yesterday, 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, 04-11-2024, 12:08 PM
    0 responses
    58 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    54 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    46 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-04-2024, 09:00 AM
    0 responses
    55 views
    0 likes
    Last Post seqadmin  
    Working...
    X