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5188- 5334 Affinity Removal System Spin Cartridge, Human Albumin, 0.45 mL
5188- 6562 Affinity Removal System Column, Human Albumin, 4.6 x 50 mm
The Multiple Affinity Removal Spin Cartridge - Human 7 removes approximately 85–90% of the total protein when used with the Multiple Affinity Removal System.
5188- 8826 Affinity Removal System Column, Human Albumin/IgG, 4.6 x 50 mm
The Multiple Affinity Removal Spin Cartridge - Human 14 removes approximately 94% of the total protein when used with the Multiple Affinity Removal System.
PDF Report Builder - remove repeating batch table
PDF Report Builder - remove repeating batch table
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I'm editing the Report Builder template "GenCalibration" - Ultimately I want to list RelativeStandardError only, for each Target Compound. So far I've been successful in removing calibration curve graphic & calibration results table, and then removed page break between each compound - result is attached! The final issue - how can I remove the repeating "BatchAttributes Table" before each "RSE table"?
Removing Cell membrane matrix from cell plate before adding PBMCs?
Removing Cell membrane matrix from cell plate before adding PBMCs?
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We noticed the other day that when loading the cells into the 96 well cell plate, some of us remove the cell membrane matrix (in our case, Geltrex) before adding the cells while others don't. Our error bars between cells are smaller when we don't remove the extra Geltrex and there is no difference in the raw data either.
How to remove contamination peaks from chromatogram through data analysis?
How to remove contamination peaks from chromatogram through data analysis?
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Fiber conditioning before and between samples did not get rid of it. I have tried to remove those peaks by extracting their spectra and doing a Subtract Background (BSB) twice. This worked but I noticed that some other peaks lost intensity. It makes sense if the fragments were removed wherever they appeared during the entire run. My question is: Is it possible to subtract a spectrum at only a specific time range?
How to remove the sequential prefix/index from PDF filenames in Quant-My-Way / MassHunter Quant?
How to remove the sequential prefix/index from PDF filenames in Quant-My-Way / MassHunter Quant?
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Hello everyone, I am currently using MassHunter Quantitative Analysis (Quant-My-Way) and facing an issue with automated PDF report generation. When generating batch reports, the software automatically adds an incremental numerical prefix to each PDF file (e.g., _014_T-3328-25.pdf instead of just T-3328-25.pdf ). Since this index is unnecessary for our workflow, we currently have to rename the files manually one by one. Is there a setting in the Method / Report Builder / Queue options to disable this default sequential prefix so that the output files are named using only the Sample Name? Thank you in advance for your help!
The Multiple Affinity Removal Spin Cartridge - Human 6 removes approximately 85–90% of the total protein when used with the Multiple Affinity Removal System.
5188- 8825 Multiple Affinity Removal System Spin Cartridge, Human Albumin/IgG, 0.45 mL
Agilent's Multiple Affinity Removal LC Column - Human 14 is designed to remove 14 abundant protein from human plasma samples.
Multiple Affinity Removal LC Column - Human 7 is designed to remove 7 interfering, high-abundance proteins from human plasma samples.
The Multiple Affinity Removal LC Column - Human 6 is designed to remove 6 abundant proteins from human plasma samples.
The Multiple Affinity Removal Spin Cartridge – Mouse 3 removes approximately 80% of the total protein when used with the Multiple Affinity Removal System.
The Multiple Affinity Removal LC Column – Mouse 3 is designed as a simple way to remove 3 interfering, high-abundance proteins from mouse plasma samples.