imagequant las 4010 imager Search Results


imagequant las 4010  (Cytiva Europe)
97
Cytiva Europe imagequant las 4010
Imagequant Las 4010, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/imagequant+las+4010+imager/pmc04059140-220-22-25?v=Cytiva+Europe
Average 97 stars, based on 1 article reviews
imagequant las 4010 - by Bioz Stars, 2026-08
97/100 stars
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imagequant las 4010 apparatus  (TotalLab Ltd)
97
TotalLab Ltd imagequant las 4010 apparatus
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Imagequant Las 4010 Apparatus, supplied by TotalLab Ltd, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/imagequant+las+4010+imager/pmc04979516-308-16-21?v=TotalLab+Ltd
Average 97 stars, based on 1 article reviews
imagequant las 4010 apparatus - by Bioz Stars, 2026-08
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las-4010 mini imaging system  (FUJIFILM)
90
FUJIFILM las-4010 mini imaging system
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Las 4010 Mini Imaging System, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/imagequant+las+4010+imager/pmc05629445-75-1-5?v=FUJIFILM
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las-4010 mini imaging system - by Bioz Stars, 2026-08
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las 4010 ccd cameras  (FUJIFILM)
90
FUJIFILM las 4010 ccd cameras
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Las 4010 Ccd Cameras, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
las 4010 ccd cameras - by Bioz Stars, 2026-08
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imagequanttm las 4010 instrument  (Cytiva Europe)
97
Cytiva Europe imagequanttm las 4010 instrument
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Imagequanttm Las 4010 Instrument, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/imagequant+las+4010+imager/10__1080_slash_1061186x__2017__1363214-71-5-9?v=Cytiva+Europe
Average 97 stars, based on 1 article reviews
imagequanttm las 4010 instrument - by Bioz Stars, 2026-08
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efka® 4015  (BASF)
90
BASF efka® 4015
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Efka® 4015, supplied by BASF, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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efka® 4015 - by Bioz Stars, 2026-08
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tektronix 4012 terminal  (Tektronix inc)
90
Tektronix inc tektronix 4012 terminal
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Tektronix 4012 Terminal, supplied by Tektronix inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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preminol 4010  (AGC Inc)
90
AGC Inc preminol 4010
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Preminol 4010, supplied by AGC Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cp 4010  (Aremco Products Inc)
90
Aremco Products Inc cp 4010
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Cp 4010, supplied by Aremco Products Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cp 4010 - by Bioz Stars, 2026-08
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cp 8970  (SEIKO PMC CORPORATION)
90
SEIKO PMC CORPORATION cp 8970
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
Cp 8970, supplied by SEIKO PMC CORPORATION, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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4010 terminal  (Tektronix inc)
90
Tektronix inc 4010 terminal
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
4010 Terminal, supplied by Tektronix inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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4010 60  (Fisher Scientific)
86
Fisher Scientific 4010 60
Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant <t>LAS</t> <t>4010</t> densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.
4010 60, supplied by Fisher Scientific, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant LAS 4010 densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.

Journal: Cell Death Discovery

Article Title: Quinazoline-based tricyclic compounds that regulate programmed cell death, induce neuronal differentiation, and are curative in animal models for excitotoxicity and hereditary brain disease

doi: 10.1038/cddiscovery.2015.27

Figure Lengend Snippet: Neuroimmunochemical signs of differentiation of PC12 cells by our different exposure protocols, applied to Strain #1 ( a – c ) and Strain #3 ( d and e ) in comparison with their vehicle controls. ( a ) A bar graph showing protein content indicative of cell size of strain #1 differentiated by glutamate, MGV-1, and MGV-1+glutamate. MGV-1+glutamate enhances protein levels in these cells sixfold. ( b ) A bar graph of relative tubulin 3 β expression in strain #1 cells differentiated by three different treatments (glutamate, MGV-1, and MGV-1+glutamate), compared with the vehicle control (undifferentiated cells). MGV-1+glutamate significantly enhances tubulin 3 β expression in these cells. ( c ) Representative western blot assay of the effects on the expression levels of tubulin 3 β of figures ( b ). ( d ) A bar graph showing significantly enhanced NeuN expression in cells of strain #3 differentiated by MGV-1+glutamate and by MGV-1+NGF+glutamate, compared with the vehicle control (undifferentiated cells). The other treatments shown (glutamate, MGV-1, NGF, NGF+MGV-1, NGF+glutamate) do not enhance NeuN expression significantly. ( e ) A representative western blot assay of NeuN expression in cells of strain #3 differentiated by our various protocols of . In ( b ) and ( d ), protein expression is given in arbitrary units (× 10 7 ) as provided the ImageQuant LAS 4010 densitometer. Data presented as means±S.E.M. For 5 a and 5 b n =4, for 5 d n =6. In all cases, statistical analysis by the Friedman ANOVA test, and Dunn's multiple comparison test as the post hoc . * P <0.05, ** P <0.01, *** P <0.001 as compared with vehicle control (control). Control, vehicle only; glu, glutamate; M, molecular weight (50 kDa MW) markers for the western blots.

Article Snippet: Binding of antibodies to the membrane was detected with the EZ-ECL-detection reagent (Biological Industries), using the ImageQuant LAS 4010 apparatus and Totallab Quant quantitative image analysis of Totallab (Newcastle upon Tyne, England).

Techniques: Comparison, Expressing, Western Blot, Molecular Weight