1 2 dioleoyl sn glycero 3 phosphoethanolamine dope Avanti Polar Search Results


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  • 95
    Millipore cardiolipin
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    Avanti Polar 1 2 dioleoyl sn glycero 3 phosphoethanolamine dope
    1 2 Dioleoyl Sn Glycero 3 Phosphoethanolamine Dope, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 99/100, based on 439 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Avanti Polar 1 2 dioleoyl sn glycero 3 phosphoethanolamine
    1 2 Dioleoyl Sn Glycero 3 Phosphoethanolamine, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 99/100, based on 101 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Avanti Polar nbd ps
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Avanti Polar nbd pa
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Avanti Polar 810150c
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Avanti Polar 1 stearoyl 2 oleoyl sn glycero 3 phosphoethanolamine
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
    1 Stearoyl 2 Oleoyl Sn Glycero 3 Phosphoethanolamine, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 80/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Avanti Polar egg liss rhod pe
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
    Egg Liss Rhod Pe, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 80/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Avanti Polar nbd pc
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Avanti Polar 1 2 dioleoyl sn glycero 3 phospho l serine dops
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
    1 2 Dioleoyl Sn Glycero 3 Phospho L Serine Dops, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 99/100, based on 143 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Avanti Polar 1 2 dioleoyl sn glycero 3 phosphoethanolamine n cap biotinyl biotin cap dope
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
    1 2 Dioleoyl Sn Glycero 3 Phosphoethanolamine N Cap Biotinyl Biotin Cap Dope, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 76/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Millipore nbd pe n nbd aminohexanoyl 1 2 dioleoyl sn glycero 3 phosphoethanolamine
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
    Nbd Pe N Nbd Aminohexanoyl 1 2 Dioleoyl Sn Glycero 3 Phosphoethanolamine, supplied by Millipore, used in various techniques. Bioz Stars score: 76/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Avanti Polar 7 nitro2 oxa 1 3 dialzol 4 yl amino dodecanoyl 1 hexadecanoyl sn glycero 3 phosphocholine nbd c12 hpc
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
    7 Nitro2 Oxa 1 3 Dialzol 4 Yl Amino Dodecanoyl 1 Hexadecanoyl Sn Glycero 3 Phosphocholine Nbd C12 Hpc, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 76/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Avanti Polar 1 palmitoyl 2 oleoyl sn glycero 3 phosphoethanolamine
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Avanti Polar 1 oleoyl 2 12
    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% <t>NBD-sphingomyelin</t> ( green ) <t>(NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol</t> 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p
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    Image Search Results


    Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% NBD-sphingomyelin ( green ) (NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p

    Journal: The Journal of Biological Chemistry

    Article Title: Lipid Polarity Is Maintained in Absence of Tight Junctions

    doi: 10.1074/jbc.M111.327064

    Figure Lengend Snippet: Binding of lysenin to sphingomyelin-containing GUVs. A , shown is the observation of a GUV containing 5 mol% NBD-sphingomyelin ( green ) (NBD-C12-SM/DOPC/SM(d18:1–16:0)/cholesterol 6:33:27:33) and RFP-lysenin ( red ) ( scale bar , 10 μm). B , shown is the observation of binding of GFP-lysenin ( green ) to a GUV of DOPC/rhodamine-DOPE (molar ratio, 99:1) ( upper panel ), SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) ( middle panel ), or SM(d18:1–16:0)/DOPC/cholesterol/rhodamine-DOPE (molar ratio, 33:33:33:1) ( lower panel ). Each GUV contained 1 mol% rhodamine-DOPE ( scale bar , 10 μm). C , the fluorescence of GFP-lysenin associated with liposome ( Y circle ) and the fluorescence of GFP-lysenin outside of the liposome ( Y env ) were quantitatively measured in each GUV. The value of Y circle / Y env of the SM(d18:1- 16:0)/DOPC/cholesterol ( Chol )/rhodamine-DOPE (molar ratio, 33:33:33:1) and SM (d18:1–16:0)/DOPC/rhodamine-DOPE (molar ratio, 49:50:1) GUVs was calculated. Data are the means ± S.D. of three independent experiments. p

    Article Snippet: The DOPC (1,2-di-oleoyl-sn-glycero-3-phosphocholine), sphingomyelin (d18:1–16:0) N -palmitoyl- d - erythro -sphingosylphosphorylcholine), cholesterol, rhodamine-DOPE (1,2-dioleoyl- sn -glycero-3-phosphoethanolamine- n -(lissamine rhodamine B sulfonyl)), C12-NBD-sphingomyelin ( N -[12-[(7-nitro-2–1,3-benzoxadiazol-4-yl)amino]lauroyl]-sphingosine-1-phosphocholine), and 18:1–06:0 NBD PS 1-oleoyl-2-{6-[(7-nitro-2–1,3-benzoxadiazol-4-yl)amino]hexanoyl}- sn -glycero-3-phosphoserine were obtained from Avanti Polar Lipids (Alabaster, AL).

    Techniques: Binding Assay, Fluorescence