sn-1-18 Search Results


sn 1 18 1 lyso pe  (Avanti Polar)
94
Avanti Polar sn 1 18 1 lyso pe
PDAT activity in microsomal preparations of Arabidopsis transformants expressing the AtPDAT gene under the control of the 35S promoter. A, PDAT activity in microsomal preparations of roots from control plants (transformed with empty vector) and three different transgenic lines expressing the AtPDAT under the control of the 35S promoter and (Top) northern-blot analysis of total root RNA from corresponding plants. PDAT activity was measured with sn-1-oleoyl(18:1)-sn-2-[14C]ricinoleoyl-PC and unlabeled di-18:1-DAG as substrates. B, PDAT activity as a function of DAG concentrations in microsomal preparations of roots from AtPDAT overexpresser (line 1-3b-44). The PDAT activity was measured with <t>sn-1-18:1-sn-2-[14C]18:3-PE</t> and with di-18:1-DAG added in amounts indicated in the figure.
Sn 1 18 1 Lyso Pe, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sn-1-18/18%3A1+Lyso+PE/pmc00519051-464-0-20
Average 94 stars, based on 1 article reviews
sn 1 18 1 lyso pe - by Bioz Stars, 2026-11
94/100 stars
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sn -1-18  (Larodan)
93
Larodan sn -1-18
PDAT activity in microsomal preparations of Arabidopsis transformants expressing the AtPDAT gene under the control of the 35S promoter. A, PDAT activity in microsomal preparations of roots from control plants (transformed with empty vector) and three different transgenic lines expressing the AtPDAT under the control of the 35S promoter and (Top) northern-blot analysis of total root RNA from corresponding plants. PDAT activity was measured with sn-1-oleoyl(18:1)-sn-2-[14C]ricinoleoyl-PC and unlabeled di-18:1-DAG as substrates. B, PDAT activity as a function of DAG concentrations in microsomal preparations of roots from AtPDAT overexpresser (line 1-3b-44). The PDAT activity was measured with <t>sn-1-18:1-sn-2-[14C]18:3-PE</t> and with di-18:1-DAG added in amounts indicated in the figure.
Sn 1 18, supplied by Larodan, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sn-1-18/Lyso-phosphatidylcholine%2C+LPC/pmc11681254-220-31-33
Average 93 stars, based on 1 article reviews
sn -1-18 - by Bioz Stars, 2026-11
93/100 stars
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sn −1-18  (Larodan)
93
Larodan sn −1-18
PDAT activity in microsomal preparations of Arabidopsis transformants expressing the AtPDAT gene under the control of the 35S promoter. A, PDAT activity in microsomal preparations of roots from control plants (transformed with empty vector) and three different transgenic lines expressing the AtPDAT under the control of the 35S promoter and (Top) northern-blot analysis of total root RNA from corresponding plants. PDAT activity was measured with sn-1-oleoyl(18:1)-sn-2-[14C]ricinoleoyl-PC and unlabeled di-18:1-DAG as substrates. B, PDAT activity as a function of DAG concentrations in microsomal preparations of roots from AtPDAT overexpresser (line 1-3b-44). The PDAT activity was measured with <t>sn-1-18:1-sn-2-[14C]18:3-PE</t> and with di-18:1-DAG added in amounts indicated in the figure.
Sn −1 18, supplied by Larodan, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sn-1-18/Lyso-phosphatidylcholine%2C+LPC/pmc12219680-54-8-24
Average 93 stars, based on 1 article reviews
sn −1-18 - by Bioz Stars, 2026-11
93/100 stars
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sn 1 18 1 lysopa  (Croda International Plc)
91
Croda International Plc sn 1 18 1 lysopa
PDAT activity in microsomal preparations of Arabidopsis transformants expressing the AtPDAT gene under the control of the 35S promoter. A, PDAT activity in microsomal preparations of roots from control plants (transformed with empty vector) and three different transgenic lines expressing the AtPDAT under the control of the 35S promoter and (Top) northern-blot analysis of total root RNA from corresponding plants. PDAT activity was measured with sn-1-oleoyl(18:1)-sn-2-[14C]ricinoleoyl-PC and unlabeled di-18:1-DAG as substrates. B, PDAT activity as a function of DAG concentrations in microsomal preparations of roots from AtPDAT overexpresser (line 1-3b-44). The PDAT activity was measured with <t>sn-1-18:1-sn-2-[14C]18:3-PE</t> and with di-18:1-DAG added in amounts indicated in the figure.
Sn 1 18 1 Lysopa, supplied by Croda International Plc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sn-1-18/18%3A1+Lyso+PA/10__1194_slash_jlr__m500435___jlr200-64-7-39
Average 91 stars, based on 1 article reviews
sn 1 18 1 lysopa - by Bioz Stars, 2026-11
91/100 stars
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sn 1 18 1 lysophosphatidylcholine  (Avanti Polar)
94
Avanti Polar sn 1 18 1 lysophosphatidylcholine
PDAT activity in microsomal preparations of Arabidopsis transformants expressing the AtPDAT gene under the control of the 35S promoter. A, PDAT activity in microsomal preparations of roots from control plants (transformed with empty vector) and three different transgenic lines expressing the AtPDAT under the control of the 35S promoter and (Top) northern-blot analysis of total root RNA from corresponding plants. PDAT activity was measured with sn-1-oleoyl(18:1)-sn-2-[14C]ricinoleoyl-PC and unlabeled di-18:1-DAG as substrates. B, PDAT activity as a function of DAG concentrations in microsomal preparations of roots from AtPDAT overexpresser (line 1-3b-44). The PDAT activity was measured with <t>sn-1-18:1-sn-2-[14C]18:3-PE</t> and with di-18:1-DAG added in amounts indicated in the figure.
Sn 1 18 1 Lysophosphatidylcholine, supplied by Avanti Polar, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sn-1-18/Thin-Layer+Chromatography/pmc08348727-434-8-23
Average 94 stars, based on 1 article reviews
sn 1 18 1 lysophosphatidylcholine - by Bioz Stars, 2026-11
94/100 stars
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anti-cxcl5 monoclonal antibody, clone sn1187-43c4  (Creative BioMart)
N/A
Involved in neutrophil activation. In vitro, ENA-78(8-78) and ENA-78(9-78) show a threefold higher chemotactic activity for neutrophil granulocytes.Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.http://www.creative-diagnostics.com/Anti-Cxcl5-MAb-162968-144.htm
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Image Search Results


PDAT activity in microsomal preparations of Arabidopsis transformants expressing the AtPDAT gene under the control of the 35S promoter. A, PDAT activity in microsomal preparations of roots from control plants (transformed with empty vector) and three different transgenic lines expressing the AtPDAT under the control of the 35S promoter and (Top) northern-blot analysis of total root RNA from corresponding plants. PDAT activity was measured with sn-1-oleoyl(18:1)-sn-2-[14C]ricinoleoyl-PC and unlabeled di-18:1-DAG as substrates. B, PDAT activity as a function of DAG concentrations in microsomal preparations of roots from AtPDAT overexpresser (line 1-3b-44). The PDAT activity was measured with sn-1-18:1-sn-2-[14C]18:3-PE and with di-18:1-DAG added in amounts indicated in the figure.

Journal:

Article Title: Cloning and Functional Characterization of a Phospholipid:Diacylglycerol Acyltransferase from Arabidopsis 1

doi: 10.1104/pp.104.044354

Figure Lengend Snippet: PDAT activity in microsomal preparations of Arabidopsis transformants expressing the AtPDAT gene under the control of the 35S promoter. A, PDAT activity in microsomal preparations of roots from control plants (transformed with empty vector) and three different transgenic lines expressing the AtPDAT under the control of the 35S promoter and (Top) northern-blot analysis of total root RNA from corresponding plants. PDAT activity was measured with sn-1-oleoyl(18:1)-sn-2-[14C]ricinoleoyl-PC and unlabeled di-18:1-DAG as substrates. B, PDAT activity as a function of DAG concentrations in microsomal preparations of roots from AtPDAT overexpresser (line 1-3b-44). The PDAT activity was measured with sn-1-18:1-sn-2-[14C]18:3-PE and with di-18:1-DAG added in amounts indicated in the figure.

Article Snippet: Sn -1-18:1-lyso-PE, and sn -1-[ 14 C]18:1-lyso-PC were obtained by phospholipase ( Naja mossambica mossambica ; Sigma) treatment of di-18:1-PE (Avanti Polar Lipids, Birmingham, AL) and di-[1- 14 C]18:1-PC, respectively, followed by purification by TLC.

Techniques: Activity Assay, Expressing, Transformation Assay, Plasmid Preparation, Transgenic Assay, Northern Blot

Autoradiogram of neutral lipid fraction separated on TLC after incubation of microsomal preparations of roots from different Arabidopsis lines with sn-1-18:1-sn-2-[14C]18:2-PE or sn-1-18:1-sn-2 -[14C]18:2-DAG in the presence of vernoloyl-DAG. A, Incubations with microsomal preparations from AtPDAT overexpresser (line 1-1-6) and control plants (transformed with empty vector). B, Incubation with microsomal preparations from AtPDAT T-DNA insertion mutant (mutant) and the null segregant (null) to this mutant. The figures given correspond to percentage radioactivity in the TAG areas of total radioactivity in the lane. Amount of substrates used in each assay: sn-1-18:1-sn-2-[14C]18:2-PE: Figure A, 2.5 nmol; Figure B, 5 nmol; sn-1-18:1-sn-2 -[14C]18:2-DAG: Figure A, 1.5 nmol; Figure B, 6 nmol; vernoloyl-DAG: Figure A, 1.5 nmol; Figure B, 6 nmol. TAG, triacylglycerol; 1-epoxy-TAG, TAG with one vernoloyl moiety; FFA, free fatty acids; DAG, diacylglycerol; MAG, monoacylglycerol; PL, polar lipids.

Journal:

Article Title: Cloning and Functional Characterization of a Phospholipid:Diacylglycerol Acyltransferase from Arabidopsis 1

doi: 10.1104/pp.104.044354

Figure Lengend Snippet: Autoradiogram of neutral lipid fraction separated on TLC after incubation of microsomal preparations of roots from different Arabidopsis lines with sn-1-18:1-sn-2-[14C]18:2-PE or sn-1-18:1-sn-2 -[14C]18:2-DAG in the presence of vernoloyl-DAG. A, Incubations with microsomal preparations from AtPDAT overexpresser (line 1-1-6) and control plants (transformed with empty vector). B, Incubation with microsomal preparations from AtPDAT T-DNA insertion mutant (mutant) and the null segregant (null) to this mutant. The figures given correspond to percentage radioactivity in the TAG areas of total radioactivity in the lane. Amount of substrates used in each assay: sn-1-18:1-sn-2-[14C]18:2-PE: Figure A, 2.5 nmol; Figure B, 5 nmol; sn-1-18:1-sn-2 -[14C]18:2-DAG: Figure A, 1.5 nmol; Figure B, 6 nmol; vernoloyl-DAG: Figure A, 1.5 nmol; Figure B, 6 nmol. TAG, triacylglycerol; 1-epoxy-TAG, TAG with one vernoloyl moiety; FFA, free fatty acids; DAG, diacylglycerol; MAG, monoacylglycerol; PL, polar lipids.

Article Snippet: Sn -1-18:1-lyso-PE, and sn -1-[ 14 C]18:1-lyso-PC were obtained by phospholipase ( Naja mossambica mossambica ; Sigma) treatment of di-18:1-PE (Avanti Polar Lipids, Birmingham, AL) and di-[1- 14 C]18:1-PC, respectively, followed by purification by TLC.

Techniques: Incubation, Transformation Assay, Plasmid Preparation, Mutagenesis, Radioactivity

Positional specificity of AtPDAT. PDAT activity was measured in microsomal preparations from leaves of Arabidopsis control plants (transformed with empty vector) and an AtPDAT overexpresser (line 1-1-6) with 5 nmol of either sn-1-[14C]18:1-sn-2-18:1-PC or sn-1-18:1-sn-2-[14C]18:1-PC.

Journal:

Article Title: Cloning and Functional Characterization of a Phospholipid:Diacylglycerol Acyltransferase from Arabidopsis 1

doi: 10.1104/pp.104.044354

Figure Lengend Snippet: Positional specificity of AtPDAT. PDAT activity was measured in microsomal preparations from leaves of Arabidopsis control plants (transformed with empty vector) and an AtPDAT overexpresser (line 1-1-6) with 5 nmol of either sn-1-[14C]18:1-sn-2-18:1-PC or sn-1-18:1-sn-2-[14C]18:1-PC.

Article Snippet: Sn -1-18:1-lyso-PE, and sn -1-[ 14 C]18:1-lyso-PC were obtained by phospholipase ( Naja mossambica mossambica ; Sigma) treatment of di-18:1-PE (Avanti Polar Lipids, Birmingham, AL) and di-[1- 14 C]18:1-PC, respectively, followed by purification by TLC.

Techniques: Activity Assay, Transformation Assay, Plasmid Preparation