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lpc-d7 18  (Croda International Plc)

 
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    Croda International Plc lpc-d7 18
    Lpc D7 18, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 94/100, based on 58 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/d7-lpc+18/18%3A1-d7+Lyso+PC/bio_rxiv__2025__10__13__682089-302-16-18
    Average 94 stars, based on 58 article reviews
    lpc-d7 18 - by Bioz Stars, 2026-09
    94/100 stars

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    other:

    Article Title: Palmitoyl-carnitine Regulates Lung Development by Promoting Pulmonary Mesenchyme Proliferation
    Article Snippet: For the quantification of lipids, internal standards such as d9-PC32:0(16:0/16:0), dimyristoyl-phosphatidylcholine, d9-PC36:1p(18:0p/18:1), d7-PE33:1(15:0/18:1), PE14:0/14:0, d9-PE36:1p(18:0p/18:1), d31-PS(16:0/18:1), d7-PG33:1(15:0/18:1), PG14:0/14:0, d7-PI33:1(15:0/18:1), d7PA33:1(15:0/18:1), PA 17:0/17:0, bis(monoacylglycero)phosphate 14:0/14:0, d5-CL 72:8(18:2)4, d8-SM d18:1/18:1, SM d18:1/12:0, ceramide d18:1/d7-15:0, ceramide d18:1/17:0, GluCer d18:1/8:0, d3-LacCer d18:1/16:0, GM3 d18:1/18:0-d3, Gb3-d18:1/17:0, SL-d18:1/17:0, d7-LPC 18:1, LPC C17:0, d7-LPE 18:1, LPE C17:0, LPA-C17:0, LPI-C17:1, LPS-C17:1, LPG-C17:1, S1P d17:1, and Sph-d17 were sourced from Avanti Polar Lipids.

    Article Title: Palmitoyl-carnitine regulates lung development by promoting pulmonary mesenchyme proliferation
    Article Snippet: For the quantification of lipids, internal standards such as d9-PC32:0(16:0/16:0), DMPC, d9-PC36:1p(18:0p/18:1), d7- PE33:1(15:0/18:1), PE14:0/14:0, d9-PE36:1p(18:0p/18:1), d31-PS(16:0/18:1), d7- PG33:1(15:0/18:1), PG14:0/14:0, d7-PI33:1(15:0/18:1), d7PA33:1(15:0/18:1), PA 460 17:0/17:0, BMP 14:0/14:0, d5-CL 72:8(18:2)4, d8-SM d18:1/18:1, SM d18:1/12:0, Cer d18:1/d7-15:0, Cer d18:1/17:0, GluCer d18:1/8:0, d3-LacCer d18:1/16:0, GM3 d18:1/18:0- d3, Gb3-d18:1/17:0, SL-d18:1/17:0, d7-LPC 18:1, LPC C17:0, d7-LPE 18:1, LPE C17:0, LPA-C17:0, LPI-C17:1, LPS-C17:1, LPG-C17:1, S1P d17:1, and Sph-d17 were sourced from Avanti Polar Lipids.



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    Albumin-associated lipids are consumed during cancer cell proliferation. A , comparison of lipid profiles across multiple lots of commercially available FBS (100% serum). B , lipid species detected in media with 10% FBS (Cytiva Lot #1), ranked by abundance. Lipids below the red line represent the bottom 1% of total lipid content. C , concentrations of individual lipid classes in media with 10% FBS used for subsequent experiments. D , fold change in concentration of the most abundant lipids, normalized to initial concentrations in media containing 10% FBS during cell proliferation. Each column represents individual lipid species over time, and the color indicates relative fold change: depleted ( blue ), no change ( red ), and increased ( white ). E , fold change in cell counts ( left ) and moving average of proliferation rate ( right ) in H1299 cells cultured in either 10% FBS or in serum-free DMEM supplemented with ITS and either LPC, LPE, or FA mix. F , average proliferation rate of cells over the entire assay. Error bars represent mean ± SD (n = 3). Statistical significance was assessed using Brown–Forsythe and Welch ANOVA tests ( F ). ns = not significant, ∗ p < 0.05. DMEM, Dulbecco's modified Eagle's medium; FA, fatty acid; FBS, fetal bovine serum; ITS, insulin–transferrin–selenium; LPC, lysophosphatidylcholine; LPE, lysophosphatidylethanolamine; PC, phosphatidylcholine; PE, phosphatidylethanolamine; SE, sterol ester; SM, sphingolipid; TAG, triacylglycerol.

    Journal: The Journal of Biological Chemistry

    Article Title: Defined media reveal the essential role of lipid scavenging in supporting cancer cell proliferation

    doi: 10.1016/j.jbc.2025.110693

    Figure Lengend Snippet: Albumin-associated lipids are consumed during cancer cell proliferation. A , comparison of lipid profiles across multiple lots of commercially available FBS (100% serum). B , lipid species detected in media with 10% FBS (Cytiva Lot #1), ranked by abundance. Lipids below the red line represent the bottom 1% of total lipid content. C , concentrations of individual lipid classes in media with 10% FBS used for subsequent experiments. D , fold change in concentration of the most abundant lipids, normalized to initial concentrations in media containing 10% FBS during cell proliferation. Each column represents individual lipid species over time, and the color indicates relative fold change: depleted ( blue ), no change ( red ), and increased ( white ). E , fold change in cell counts ( left ) and moving average of proliferation rate ( right ) in H1299 cells cultured in either 10% FBS or in serum-free DMEM supplemented with ITS and either LPC, LPE, or FA mix. F , average proliferation rate of cells over the entire assay. Error bars represent mean ± SD (n = 3). Statistical significance was assessed using Brown–Forsythe and Welch ANOVA tests ( F ). ns = not significant, ∗ p < 0.05. DMEM, Dulbecco's modified Eagle's medium; FA, fatty acid; FBS, fetal bovine serum; ITS, insulin–transferrin–selenium; LPC, lysophosphatidylcholine; LPE, lysophosphatidylethanolamine; PC, phosphatidylcholine; PE, phosphatidylethanolamine; SE, sterol ester; SM, sphingolipid; TAG, triacylglycerol.

    Article Snippet: LPE 18:1 (846725P), LPE 16:0 (856705P), LPC 18:1-d7 (791643), LPE 18:1-d7 (791644), and lipids used to generate calibration curves SPLASH LIPIDOMIX Mass Spec Standard (330707), LightSPLASH LIPIDOMIX Quantitative Mass Spectrometry (MS) Primary Standard (330732) were purchased from Avanti Polar Lipids.

    Techniques: Comparison, Concentration Assay, Cell Culture, Modification