Seqanswers Leaderboard Ad

Collapse

Announcement

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

  • Nextera Rapid capture- Reagent reduction

    Hello,

    I have gone through some posts and found interesting topic regarding the use of half reagents.

    We in our lab are doing Nextera Rapid capture enrichment method (custom probes) on the miseq using V2 chemistry. Now we want to reduce our cost since the number of samples are being increased.

    so is there any way to reduce the amount of the reagents mentioned in the protocol or change? what steps or concentration of reagents can be modified in the nextera protocol.

    If the reagents are reduced to half , will there be any impact on cluster density and sequencing quality itself? how many samples can be multiplexed with reduced reagents?

    Any help or suggestions would be appreciated?

    Thankyou in advance

  • #2
    Hello sanju0891.
    We are also intrested in this topic. I think that it can be done. However we tried this approach only in the tagmentase step.
    I don't think that you'll suffer an impact on cluster density if you perform a reliable qPCR step.
    I would like to take a look into the post that you are refering to.

    Regards

    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 on Modified Bases...
      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
    55 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 10:19 PM
    0 responses
    52 views
    0 likes
    Last Post seqadmin  
    Started by seqadmin, 04-10-2024, 09:21 AM
    0 responses
    45 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