ABCA1 p.Val93Cys

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PMID: 18359958 [PubMed] Faulkner LE et al: "An analysis of the role of a retroendocytosis pathway in ABCA1-mediated cholesterol efflux from macrophages."
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131 The V93C mutant was chosen for further studies because it exhibited the highest levels of expression in our recombinant system.
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ABCA1 p.Val93Cys 18359958:131:4
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132 1324 Journal of Lipid Research Volume 49, 2008 atHealthScienceLibraryCB#7585,onSeptember24,2012www.jlr.orgDownloadedfrom 0.DC1.html Next, the ability to visualize fluorescent apoA-I (V93C) within RAW264.7 macrophages treated with cAMP to induce expression of ABCA1 was assessed.
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ABCA1 p.Val93Cys 18359958:132:149
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ABCA1 p.Val93Cys 18359958:132:184
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133 Panels 1 and 2 of Fig. 2A show an optical slice taken through the center of the macrophage by confocal microscopy after incubation with fluorescent apoA-I (V93C) for 2 h.
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ABCA1 p.Val93Cys 18359958:133:156
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143 To evaluate this possibility, the effect of cAMP treatment on the uptake of dextran polymers labeled with the identical Alexa Fluor 546 probe as that present on our apoA-I (V93C) was studied.
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ABCA1 p.Val93Cys 18359958:143:173
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181 Colocalization of Alexa Fluor apoA-I (V93C) with LysoTracker Green in RAW cells.
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ABCA1 p.Val93Cys 18359958:181:38
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190 Then, either 10 mg/ml Alexa Fluor-labeled apoA-I (V93C) 6 400 mg/ml unlabeled apoA-I competitor, or 18 mg/ml Alexa Fluor-labeled dextran beads were added 6 0.3 mM cAMP for 2 h.
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ABCA1 p.Val93Cys 18359958:190:50
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224 Pulse-chase incubation of Alexa Fluor apoA-I (V93C) in RAW cells.
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ABCA1 p.Val93Cys 18359958:224:46
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223 Pulse-chase incubation of Alexa Fluor apoA-I (V93C) in RAW cells.
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ABCA1 p.Val93Cys 18359958:223:46
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PMID: 15358601 [PubMed] Le Goff W et al: "Cyclosporin A traps ABCA1 at the plasma membrane and inhibits ABCA1-mediated lipid efflux to apolipoprotein A-I."
No. Sentence Comment
50 ApoAI Uptake, Degradation, and Resecretion Assay Radiolabeling of 140 ␮g of human ApoAI (specific activity 3620 cpm/ng) and assay of [125 I]apoAI uptake, degradation, and resecretion were performed as previously described.21 Uptake of Alexa568-labeled apoAI, processing, fixation, and DAPI counterstaining were as previously described,19 with the following modifications: an N-terminal His tagged ApoAI V93C substitution was created and purified by standard methods22 and labeled with Alexa 568 Maleimide (Molecular Probes).
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ABCA1 p.Val93Cys 15358601:50:410
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44 ApoAI Uptake, Degradation, and Resecretion Assay Radiolabeling of 140 òe;g of human ApoAI (specific activity 3620 cpm/ng) and assay of [125 I]apoAI uptake, degradation, and resecretion were performed as previously described.21 Uptake of Alexa568-labeled apoAI, processing, fixation, and DAPI counterstaining were as previously described,19 with the following modifications: an N-terminal His tagged ApoAI V93C substitution was created and purified by standard methods22 and labeled with Alexa 568 Maleimide (Molecular Probes).
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ABCA1 p.Val93Cys 15358601:44:409
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