Published customer image: LYNX Rapid Fluorescein Antibody Conjugation Kit (LNK061F) used for conjugation of anti Cyp11a1 antibody to fluorescein and subsequent use in flow cytometry.Image caption:The Steroid Synthesis Pathway in Th2 Cells Produces Pregnenolone: Steroid Production In Vitro during Th2 Polarization and In Vivo, in Response to Helminth Infection: (A) Quantitative detection of pregnenolone by LC-MS/MS. Naive Th cells were cultured in Th1 or Th2 activation-differentiation conditions. After 3 days of stimulation, cells were rested for 2 days with equal cell density. Cell supernatants were extracted for steroid profiling. Bars represent the mean pregnenolone concentration ±SEM. p values were calculated by unpaired two-tailed t test. (B) Quantitative detection of pregnenolone by competitive ELISA. Th cells were stimulated for 3 days and rested for 3 days before supernatants were analyzed by competitive ELISA. Bars represent the mean concentration ±SEM from four independent experiments. p values were calculated using the unpaired two-tailed t test. (C) Th2 supernatants were analyzed by ELISA for pregnenolone production as described in (B) with or without the presence of Cyp11a1 inhibitor, aminoglutethimide (AG). p values were calculated by unpaired two-tailed t test. Error bars are SDs from the mean. (D) Schematic flowchart of in vivo experimental design. C57BL/6 mice were infected wi
LYNX RAPID FLUORESCEIN ANTIBODY CONJUGATION KIT
Published customer image: LYNX Rapid Fluorescein Antibody Conjugation Kit (LNK061) used for conjugation of anti Cyp11a1 antibody to fluoriscein and subsequent use in flow cytometryImage caption:The Steroid Synthesis Pathway in Th2 Cells Produces Pregnenolone: Steroid Production In Vitro during Th2 Polarization and In Vivo, in Response to Helminth Infection: (A) Quantitative detection of pregnenolone by LC-MS/MS. Naive Th cells were cultured in Th1 or Th2 activation-differentiation conditions. After 3 days of stimulation, cells were rested for 2 days with equal cell density. Cell supernatants were extracted for steroid profiling. Bars represent the mean pregnenolone concentration ±SEM. p values were calculated by unpaired two-tailed t test. (B) Quantitative detection of pregnenolone by competitive ELISA. Th cells were stimulated for 3 days and rested for 3 days before supernatants were analyzed by competitive ELISA. Bars represent the mean concentration ±SEM from four independent experiments. p values were calculated using the unpaired two-tailed t test. (C) Th2 supernatants were analyzed by ELISA for pregnenolone production as described in (B) with or without the presence of Cyp11a1 inhibitor, aminoglutethimide (AG). p values were calculated by unpaired two-tailed t test. Error bars are SDs from the mean. (D) Schematic flowchart of in vivo experimental design. C57BL/6 mice were infected with nematode larvae
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