m l fucose Search Results


m l fucose pbst  (Vector Laboratories)
94
Vector Laboratories m l fucose pbst
M L Fucose Pbst, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fura-2ff-am  (Thermo Fisher)
90
Thermo Fisher fura-2ff-am
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
Fura 2ff Am, supplied by Thermo Fisher, 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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fluorinated gdp l fucose analog  (Santa Cruz Biotechnology)
92
Santa Cruz Biotechnology fluorinated gdp l fucose analog
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
Fluorinated Gdp L Fucose Analog, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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2 deoxy 2 fluoro l fucose  (Santa Cruz Biotechnology)
91
Santa Cruz Biotechnology 2 deoxy 2 fluoro l fucose
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
2 Deoxy 2 Fluoro L Fucose, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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m l fucose  (Biosynth Carbosynth)
99
Biosynth Carbosynth m l fucose
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
M L Fucose, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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m l fucose  (Vector Laboratories)
93
Vector Laboratories m l fucose
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
M L Fucose, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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l-fucose  (Millipore)
90
Millipore l-fucose
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
L Fucose, supplied by Millipore, 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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fura-2ff/am  (TEFLabs Inc)
90
TEFLabs Inc fura-2ff/am
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
Fura 2ff/Am, supplied by TEFLabs 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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fura-2ff/am - by Bioz Stars, 2026-04
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gdp-l-fucose  (Millipore)
90
Millipore gdp-l-fucose
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
Gdp L Fucose, supplied by Millipore, 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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chemical inhibitor 2 deoxy 2 fluoro l fucose  (Biosynth Carbosynth)
96
Biosynth Carbosynth chemical inhibitor 2 deoxy 2 fluoro l fucose
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
Chemical Inhibitor 2 Deoxy 2 Fluoro L Fucose, supplied by Biosynth Carbosynth, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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0.7 m l-fucose  (Millipore)
90
Millipore 0.7 m l-fucose
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
0.7 M L Fucose, supplied by Millipore, 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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fura-2ff  (Billups Inc)
90
Billups Inc fura-2ff
Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of <t>Fura-2FF-loaded</t> hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).
Fura 2ff, supplied by Billups 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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Image Search Results


Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of Fura-2FF-loaded hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).

Journal: The Journal of Biological Chemistry

Article Title: Calcium/Calmodulin-dependent Protein Kinase II (CaMKII) Inhibition Induces Neurotoxicity via Dysregulation of Glutamate/Calcium Signaling and Hyperexcitability *

doi: 10.1074/jbc.M111.323915

Figure Lengend Snippet: Calcium dysregulation with CaMKII inhibition in hippocampal neurons. A, representative bright field; B and C, fluorescent images of Fura-2FF-loaded hippocampal neurons. B, before treatment; C, after treatment with 10 μm tat-CN21. D, cytoplasmic calcium levels ([Ca2+]c) (mean ± S.E.) before and after application of 10 μm tat-CN21, tat-CN21Ala, or tat. E, neuronal intracellular calcium levels (mean ± S.E.) before (−300 to 0 s) and after (0 to 1200 s) application of 10 μm tat-CN21, tat-CN21Ala, or tat, as measured by Fluo-4 (n = 4). F, average integral of fluorescent intensity from 0 to 1200 s in E (mean ± S.E., n = 3–6) with application of CaMKII inhibitors with and without pharmacological blockers of neuronal excitability. The integral was normalized to the calcium influx observed with application of 10 μm tat-CN21. *, p < 0.05 compared with tat-CN21 alone (one-way ANOVA, post hoc Dunnett's test).

Article Snippet: Calcium Imaging Hippocampal neurons 10–12 DIV were loaded with 2.6 μ m Fura-2FF-AM (Invitrogen) and 1.7 μ m Rhodamine 123 and subsequently imaged as described previously ( 20 , 22 ).

Techniques: Inhibition