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14:0-6:0(C2 NBD) PI(4,5)P2 TEA

Catalog No.: B11248
Fluorescent Lipid
14:0-6:0(C2 NBD) PI(4,5)P2 TEA is a fluorescent phosphoinositide labeled with Nitrobenzoxadiazole (NBD), exhibiting excitation and emission maxima at 460 nm and 540 nm, respectively. This compound is useful for studying lipid signaling pathways and membrane dynamics in various biological systems. Its fluorescent properties enable visualization of phosphoinositide localization and interactions in cellular contexts, making it an essential tool for researchers investigating cell signaling mechanisms.
14:0-6:0(C2 NBD) PI(4,5)P2 TEA 3091879-57-8 Fluorescent Lipid
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Research use only. We do not sell to patients.
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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
Description14:0-6:0(C2 NBD) PI(4,5)P2 TEA is a fluorescent phosphoinositide labeled with Nitrobenzoxadiazole (NBD), exhibiting excitation and emission maxima at 460 nm and 540 nm, respectively. This compound is useful for studying lipid signaling pathways and membrane dynamics in various biological systems. Its fluorescent properties enable visualization of phosphoinositide localization and interactions in cellular contexts, making it an essential tool for researchers investigating cell signaling mechanisms.
Product Information
Catalog NumB11248
FormulaC55H107N8O23P3
Molecular Weight1341.40
CAS Number3091879-57-8
SMILESCC[NH+](CC)CC.CC[NH+](CC)CC.CC[NH+](CC)CC.[H][C@@](COP([O-])(OC1C(O)C(OP([O-])(O)=O)C(OP([O-])(O)=O)C(O)[C@H]1O)=O)(OC(CCCCCNC(CNC2=CC=C([N+]([O-])=O)C3=NON=C23)=O)=O)COC(CCCCCCCCCCCCC)=O
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