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electropherogram analysis software  (OriginLab corp)
90
OriginLab corp electropherogram analysis software
Optimization of separation buffer conditions to separate C16 lipid metabolites. <t>Electropherograms</t> of three analytes separated in different separation buffers; peak 1 is C16-PI(3,4)P2, peak 2 is C16-PI(4,5)P2, and peak 3 is C16-PI(3,4,5)P3. Separation buffers of (A) 32 mM NaH2PO4, pH 7.3 + 20% 1-propanol [49], (B) 200 mM NaH2PO4, pH 8.3 + 15% 2-propanol, and (C) 80 mM NaH2PO4, pH 6.8 + 15% 2-propanol. (D) Resolution (R) and theoretical plates (N) for analyte separations in the different separation buffers.
Electropherogram Analysis Software, supplied by OriginLab corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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electropherogram analysis software - by Bioz Stars, 2026-03
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phred electropherogram quality analysis software  (ASPAR PHARMACEUTICALS LIMITED)
90
ASPAR PHARMACEUTICALS LIMITED phred electropherogram quality analysis software
Optimization of separation buffer conditions to separate C16 lipid metabolites. <t>Electropherograms</t> of three analytes separated in different separation buffers; peak 1 is C16-PI(3,4)P2, peak 2 is C16-PI(4,5)P2, and peak 3 is C16-PI(3,4,5)P3. Separation buffers of (A) 32 mM NaH2PO4, pH 7.3 + 20% 1-propanol [49], (B) 200 mM NaH2PO4, pH 8.3 + 15% 2-propanol, and (C) 80 mM NaH2PO4, pH 6.8 + 15% 2-propanol. (D) Resolution (R) and theoretical plates (N) for analyte separations in the different separation buffers.
Phred Electropherogram Quality Analysis Software, supplied by ASPAR PHARMACEUTICALS LIMITED, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/phred electropherogram quality analysis software/product/ASPAR PHARMACEUTICALS LIMITED
Average 90 stars, based on 1 article reviews
phred electropherogram quality analysis software - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

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Optimization of separation buffer conditions to separate C16 lipid metabolites. Electropherograms of three analytes separated in different separation buffers; peak 1 is C16-PI(3,4)P2, peak 2 is C16-PI(4,5)P2, and peak 3 is C16-PI(3,4,5)P3. Separation buffers of (A) 32 mM NaH2PO4, pH 7.3 + 20% 1-propanol [49], (B) 200 mM NaH2PO4, pH 8.3 + 15% 2-propanol, and (C) 80 mM NaH2PO4, pH 6.8 + 15% 2-propanol. (D) Resolution (R) and theoretical plates (N) for analyte separations in the different separation buffers.

Journal: Journal of chromatography. A

Article Title: Chemical Fixation to Arrest Phospholipid Signaling for Chemical Cytometry

doi: 10.1016/j.chroma.2017.05.022

Figure Lengend Snippet: Optimization of separation buffer conditions to separate C16 lipid metabolites. Electropherograms of three analytes separated in different separation buffers; peak 1 is C16-PI(3,4)P2, peak 2 is C16-PI(4,5)P2, and peak 3 is C16-PI(3,4,5)P3. Separation buffers of (A) 32 mM NaH2PO4, pH 7.3 + 20% 1-propanol [49], (B) 200 mM NaH2PO4, pH 8.3 + 15% 2-propanol, and (C) 80 mM NaH2PO4, pH 6.8 + 15% 2-propanol. (D) Resolution (R) and theoretical plates (N) for analyte separations in the different separation buffers.

Article Snippet: Electropherograms were plotted and analyzed utilizing OriginLab 9.0.

Techniques: