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  • xie186
    replied
    Hi @egotistdown, I am wondering whether you figured out the reason. I encountered the same issue. Thanks.

    Leave a comment:


  • 10x 5' GEX - overrepresentation of RT Primer in results

    Hi all -

    First time post so apologies if this is the wrong spot..!

    I'm having issues with my first 10x 5' gene expression run and am looking for help troubleshooting what went wrong.

    The sequencing resulted in a low percentage of reads mapping to the transcriptome (~30%). Further investigation revealed an over-expression of RT Primer in Read 2. Read 1 appeared fine.

    We loaded 8000 cells and detected 6000-9000 cells (in 4 samples). Knee-plots looked good, with not much background or degraded RNA. Bioanalyzer traces taken after cDNA amplification and after library completion both looked ok.

    Samples were PBMCs treated for 18 hours with exosomes.

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    Current Approaches to Protein Sequencing
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    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...
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