4660 Search Results


93
Bio-Rad goat anti glucagon
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https://www.bioz.com/product/4660/Goat+anti+Glucagon+(N-Terminal)/pmc02848149-154-35-37
Average 93 stars, based on 1 article reviews
goat anti glucagon - by Bioz Stars, 2026-10
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ATCC l reuteri atcc pta 4660 p3
L Reuteri Atcc Pta 4660 P3, supplied by ATCC, 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
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93
Tocris kbsrc4
( A ) Quantification (upper panel) and representative Western blot (lower panel) of active Ras pulled-down vs total Ras from hippocampal slice cultures after inducing different chemical plasticity protocols. Both Ras bands were quantified together and results were normalized to control, non-stimulated slices (dashed line) and expressed as mean ± SEM, n = 5–13 independent slice batches; individual values are also represented. One-way ANOVA [F(5,42) = 23.7, p < 0.0001] + Dunnett’s post-test (*) was used to evaluate Ras activation compared to control. ( B ) Time course of Ras activity upon DHPG stimulation in spines (blue, n = 50) and dendrites (orange, n = 15) of CA1 pyramidal cells ( n = 10) evaluated by FRET. Results are represented as mean ± SEM. Representative images of the FRET signal from dendritic branches of CA1 neurons coexpressing H-Ras-GFP and FRas2-M obtained during the time course are shown. Scale bars 2 μm. White arrows point dendritic spines. Kruskal–Wallis [H(11,571) = 53.8, p < 0.0001 for spines, and H(11,178) = 14.1, p = 0.2 for dendrites] + Dunn’s post-test (*) was used to evaluate differences across time (comparing to baseline). ( C ) Quantification (upper panel) and representative Western blot (lower panel) of phospho-Erk (pErk) and Erk signals from hippocampal slices treated with vehicle (DMSO) or inhibitors of CaMKII (KN93), Src family (PP2) or PKC (GF109203) in response to DHPG stimulation (green columns). The phospho-to-total ratio was calculated and normalized to DMSO control condition. Results are expressed as mean ± SEM and individual values are also represented, n = 4–8 independent slice batches. Mixed effects analysis [F(1,7) = 30.0, p = 0.0009] + Sidak’s post-test (*) was used to evaluate DHPG effect for each condition. ( D ) Quantification (upper panel) and representative Western blot (lower panel) of active Ras pulled-down vs total Ras from hippocampal slice cultures treated with vehicle DMSO or PP2 and stimulated with DHPG. Results are normalized to vehicle non-stimulated slices and expressed as mean ± SEM, n = 4 independent slice batches; individual values are also represented. Mixed effects analysis [F(1,6) = 18.6, p = 0.005] + Sidak’s post-test (*) was used to evaluate DHPG effect for each condition. ( E ) Time course (left) of normalized AMPAR-mediated EPSCs from baseline to 40 min after mGluR-LTD induction (PP-LFS, 1 Hz) from organotypic slices treated with DMSO (gray), Src family inhibitor PP2 (blue) or c-Src inhibitor <t>KBSRC4</t> (pink). Representative traces are shown for baseline responses (dashed line) and for the last 10 min of the recording (thick line). Quantification (right) of the extent of depression 30–40 min after induction. Results are normalized to baseline and expressed as mean ± SEM; individual values are also represented. Wilcoxon signed-rank test (#) was used to assess statistically the extent of depression. Kruskal–Wallis [H(2,39) = 8.2, p = 0.02] + Dunn’s post-test (*) was used to evaluate significant differences between conditions. ns, non-significant. .
Kbsrc4, supplied by Tocris, 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/4660/KB+SRC+4/pmc11961722-47-0-2
Average 93 stars, based on 1 article reviews
kbsrc4 - by Bioz Stars, 2026-10
93/100 stars
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94
Tocris kb src 4
( A ) Quantification (upper panel) and representative Western blot (lower panel) of active Ras pulled-down vs total Ras from hippocampal slice cultures after inducing different chemical plasticity protocols. Both Ras bands were quantified together and results were normalized to control, non-stimulated slices (dashed line) and expressed as mean ± SEM, n = 5–13 independent slice batches; individual values are also represented. One-way ANOVA [F(5,42) = 23.7, p < 0.0001] + Dunnett’s post-test (*) was used to evaluate Ras activation compared to control. ( B ) Time course of Ras activity upon DHPG stimulation in spines (blue, n = 50) and dendrites (orange, n = 15) of CA1 pyramidal cells ( n = 10) evaluated by FRET. Results are represented as mean ± SEM. Representative images of the FRET signal from dendritic branches of CA1 neurons coexpressing H-Ras-GFP and FRas2-M obtained during the time course are shown. Scale bars 2 μm. White arrows point dendritic spines. Kruskal–Wallis [H(11,571) = 53.8, p < 0.0001 for spines, and H(11,178) = 14.1, p = 0.2 for dendrites] + Dunn’s post-test (*) was used to evaluate differences across time (comparing to baseline). ( C ) Quantification (upper panel) and representative Western blot (lower panel) of phospho-Erk (pErk) and Erk signals from hippocampal slices treated with vehicle (DMSO) or inhibitors of CaMKII (KN93), Src family (PP2) or PKC (GF109203) in response to DHPG stimulation (green columns). The phospho-to-total ratio was calculated and normalized to DMSO control condition. Results are expressed as mean ± SEM and individual values are also represented, n = 4–8 independent slice batches. Mixed effects analysis [F(1,7) = 30.0, p = 0.0009] + Sidak’s post-test (*) was used to evaluate DHPG effect for each condition. ( D ) Quantification (upper panel) and representative Western blot (lower panel) of active Ras pulled-down vs total Ras from hippocampal slice cultures treated with vehicle DMSO or PP2 and stimulated with DHPG. Results are normalized to vehicle non-stimulated slices and expressed as mean ± SEM, n = 4 independent slice batches; individual values are also represented. Mixed effects analysis [F(1,6) = 18.6, p = 0.005] + Sidak’s post-test (*) was used to evaluate DHPG effect for each condition. ( E ) Time course (left) of normalized AMPAR-mediated EPSCs from baseline to 40 min after mGluR-LTD induction (PP-LFS, 1 Hz) from organotypic slices treated with DMSO (gray), Src family inhibitor PP2 (blue) or c-Src inhibitor <t>KBSRC4</t> (pink). Representative traces are shown for baseline responses (dashed line) and for the last 10 min of the recording (thick line). Quantification (right) of the extent of depression 30–40 min after induction. Results are normalized to baseline and expressed as mean ± SEM; individual values are also represented. Wilcoxon signed-rank test (#) was used to assess statistically the extent of depression. Kruskal–Wallis [H(2,39) = 8.2, p = 0.02] + Dunn’s post-test (*) was used to evaluate significant differences between conditions. ns, non-significant. .
Kb Src 4, supplied by Tocris, 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/4660/KB+SRC+4/pmc05031503-131-22-25
Average 94 stars, based on 1 article reviews
kb src 4 - by Bioz Stars, 2026-10
94/100 stars
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86
DSMZ dsm4660 t c 35 59 1 45
PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics
Dsm4660 T C 35 59 1 45, supplied by DSMZ, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/4660/Desulfatiglans+anilini/pmc00134748-213-66-119
Average 86 stars, based on 1 article reviews
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95
Chem Impex International methylhydroquinone
PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics
Methylhydroquinone, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Monsanto Technology LLC ad-67
PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics
Ad 67, supplied by Monsanto Technology LLC, 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/4660/ad+67+or+mon+4660/us12286425-126-122-126
Average 90 stars, based on 1 article reviews
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BEI Resources mpxv 4660 cell
PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics
Mpxv 4660 Cell, supplied by BEI Resources, 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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OI Analytical purge-and-trap sample concentrator eclipse 4760
PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics
Purge And Trap Sample Concentrator Eclipse 4760, supplied by OI Analytical, 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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OI Analytical oi analytical model 4660 eclipse purge-and-trap sample concentrator
PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics
Oi Analytical Model 4660 Eclipse Purge And Trap Sample Concentrator, supplied by OI Analytical, 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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PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics
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OI Analytical p&t apparatus eclipse 4660
PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics
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Image Search Results


( A ) Quantification (upper panel) and representative Western blot (lower panel) of active Ras pulled-down vs total Ras from hippocampal slice cultures after inducing different chemical plasticity protocols. Both Ras bands were quantified together and results were normalized to control, non-stimulated slices (dashed line) and expressed as mean ± SEM, n = 5–13 independent slice batches; individual values are also represented. One-way ANOVA [F(5,42) = 23.7, p < 0.0001] + Dunnett’s post-test (*) was used to evaluate Ras activation compared to control. ( B ) Time course of Ras activity upon DHPG stimulation in spines (blue, n = 50) and dendrites (orange, n = 15) of CA1 pyramidal cells ( n = 10) evaluated by FRET. Results are represented as mean ± SEM. Representative images of the FRET signal from dendritic branches of CA1 neurons coexpressing H-Ras-GFP and FRas2-M obtained during the time course are shown. Scale bars 2 μm. White arrows point dendritic spines. Kruskal–Wallis [H(11,571) = 53.8, p < 0.0001 for spines, and H(11,178) = 14.1, p = 0.2 for dendrites] + Dunn’s post-test (*) was used to evaluate differences across time (comparing to baseline). ( C ) Quantification (upper panel) and representative Western blot (lower panel) of phospho-Erk (pErk) and Erk signals from hippocampal slices treated with vehicle (DMSO) or inhibitors of CaMKII (KN93), Src family (PP2) or PKC (GF109203) in response to DHPG stimulation (green columns). The phospho-to-total ratio was calculated and normalized to DMSO control condition. Results are expressed as mean ± SEM and individual values are also represented, n = 4–8 independent slice batches. Mixed effects analysis [F(1,7) = 30.0, p = 0.0009] + Sidak’s post-test (*) was used to evaluate DHPG effect for each condition. ( D ) Quantification (upper panel) and representative Western blot (lower panel) of active Ras pulled-down vs total Ras from hippocampal slice cultures treated with vehicle DMSO or PP2 and stimulated with DHPG. Results are normalized to vehicle non-stimulated slices and expressed as mean ± SEM, n = 4 independent slice batches; individual values are also represented. Mixed effects analysis [F(1,6) = 18.6, p = 0.005] + Sidak’s post-test (*) was used to evaluate DHPG effect for each condition. ( E ) Time course (left) of normalized AMPAR-mediated EPSCs from baseline to 40 min after mGluR-LTD induction (PP-LFS, 1 Hz) from organotypic slices treated with DMSO (gray), Src family inhibitor PP2 (blue) or c-Src inhibitor KBSRC4 (pink). Representative traces are shown for baseline responses (dashed line) and for the last 10 min of the recording (thick line). Quantification (right) of the extent of depression 30–40 min after induction. Results are normalized to baseline and expressed as mean ± SEM; individual values are also represented. Wilcoxon signed-rank test (#) was used to assess statistically the extent of depression. Kruskal–Wallis [H(2,39) = 8.2, p = 0.02] + Dunn’s post-test (*) was used to evaluate significant differences between conditions. ns, non-significant. .

Journal: The EMBO Journal

Article Title: Different Ras isoforms regulate synaptic plasticity in opposite directions

doi: 10.1038/s44318-025-00390-8

Figure Lengend Snippet: ( A ) Quantification (upper panel) and representative Western blot (lower panel) of active Ras pulled-down vs total Ras from hippocampal slice cultures after inducing different chemical plasticity protocols. Both Ras bands were quantified together and results were normalized to control, non-stimulated slices (dashed line) and expressed as mean ± SEM, n = 5–13 independent slice batches; individual values are also represented. One-way ANOVA [F(5,42) = 23.7, p < 0.0001] + Dunnett’s post-test (*) was used to evaluate Ras activation compared to control. ( B ) Time course of Ras activity upon DHPG stimulation in spines (blue, n = 50) and dendrites (orange, n = 15) of CA1 pyramidal cells ( n = 10) evaluated by FRET. Results are represented as mean ± SEM. Representative images of the FRET signal from dendritic branches of CA1 neurons coexpressing H-Ras-GFP and FRas2-M obtained during the time course are shown. Scale bars 2 μm. White arrows point dendritic spines. Kruskal–Wallis [H(11,571) = 53.8, p < 0.0001 for spines, and H(11,178) = 14.1, p = 0.2 for dendrites] + Dunn’s post-test (*) was used to evaluate differences across time (comparing to baseline). ( C ) Quantification (upper panel) and representative Western blot (lower panel) of phospho-Erk (pErk) and Erk signals from hippocampal slices treated with vehicle (DMSO) or inhibitors of CaMKII (KN93), Src family (PP2) or PKC (GF109203) in response to DHPG stimulation (green columns). The phospho-to-total ratio was calculated and normalized to DMSO control condition. Results are expressed as mean ± SEM and individual values are also represented, n = 4–8 independent slice batches. Mixed effects analysis [F(1,7) = 30.0, p = 0.0009] + Sidak’s post-test (*) was used to evaluate DHPG effect for each condition. ( D ) Quantification (upper panel) and representative Western blot (lower panel) of active Ras pulled-down vs total Ras from hippocampal slice cultures treated with vehicle DMSO or PP2 and stimulated with DHPG. Results are normalized to vehicle non-stimulated slices and expressed as mean ± SEM, n = 4 independent slice batches; individual values are also represented. Mixed effects analysis [F(1,6) = 18.6, p = 0.005] + Sidak’s post-test (*) was used to evaluate DHPG effect for each condition. ( E ) Time course (left) of normalized AMPAR-mediated EPSCs from baseline to 40 min after mGluR-LTD induction (PP-LFS, 1 Hz) from organotypic slices treated with DMSO (gray), Src family inhibitor PP2 (blue) or c-Src inhibitor KBSRC4 (pink). Representative traces are shown for baseline responses (dashed line) and for the last 10 min of the recording (thick line). Quantification (right) of the extent of depression 30–40 min after induction. Results are normalized to baseline and expressed as mean ± SEM; individual values are also represented. Wilcoxon signed-rank test (#) was used to assess statistically the extent of depression. Kruskal–Wallis [H(2,39) = 8.2, p = 0.02] + Dunn’s post-test (*) was used to evaluate significant differences between conditions. ns, non-significant. .

Article Snippet: KBSRC4 , Tocris , #4660.

Techniques: Western Blot, Control, Activation Assay, Activity Assay

Reagents and tools table

Journal: The EMBO Journal

Article Title: Different Ras isoforms regulate synaptic plasticity in opposite directions

doi: 10.1038/s44318-025-00390-8

Figure Lengend Snippet: Reagents and tools table

Article Snippet: KBSRC4 , Tocris , #4660.

Techniques: Recombinant, Plasmid Preparation, Sequencing, Software, Microscopy

PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics

Journal:

Article Title: Phylogenetic Analysis Reveals Multiple Lateral Transfers of Adenosine-5?-Phosphosulfate Reductase Genes among Sulfate-Reducing Microorganisms

doi: 10.1128/JB.184.1.278-289.2002

Figure Lengend Snippet: PCR amplification of apsA gene fragments using genomic DNA of sulfate-reducing reference strains and selected characteristics

Article Snippet: 60 64 + + (45) + (59) + (59) AF418144 L27426 AF418194 Desulfacinum hydrothermale DSM13146 T C 60 59.5 + + (45) + (50) AF418148 AF170417 “ Nitrospinaceae ” a Desulfomonile tiedjei DSM6799 T C 37 49 + + (45) + (45) + (50) AF418162 M26635 AF334595 “Desulfarculus baarsii” DSM2075 T C 37 66 + + (45) + (45) + (55) AF418149 AF418174 AF334600 “Desulfobacterium anilini” DSM4660 T C 35 59.1 − + (45) + (45) + (45) AF418158 AJ237601 Desulfobacca acetoxidans DSM11109 T C 37 51.5 − − (48) − (45) − (45) Open in a separate window a Phylum and family names according to the taxonomic outline of Bergey’s Manual of Systematic Bacteriology ( http://www.cme.msu.edu/Bergeys/april2001-genus.pdf ). b DSMZ strain numbers.

Techniques: Amplification