fj-b staining fj-b Search Results


94
Biosensis ltd fjb
Fjb, supplied by Biosensis ltd, 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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Merck KGaA fjb staining kit
Fjb Staining Kit, supplied by Merck KGaA, 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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Histochem Inc fj-b staining fj-b
Fj B Staining Fj B, supplied by Histochem 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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Histochem Inc fjb (histochem inc.) staining solution
Fjb (Histochem Inc.) Staining Solution, supplied by Histochem 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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FD NeuroTechnologies tissue sectioning and fjb staining
Neuropathology as determined <t>by</t> <t>FJB-staining.</t> Animal groups included injured (POX = paraoxon, n = 7), treated (paraoxon plus ILE given 30 min later, n = 8) and naïve control (cannula implantation, but no other treatment, n = 5). Panel (A) : FJB severity scores in each animal in the study. Error bars show the standard deviation in each brain area among the tissue sections for each animal. Results for each animal are based on observations in 14–20 tissue sections (some areas, including the nucleus reuniens, are only visible in a limited rostro-caudal extent and so fewer tissue sections contribute to the neuropathology score). Animal identification numbers and experimental groups are shown on the X-axis, and FJB scores (from 0–10) are given on the Y-axis. In the ILE-treated rats, very minor FJB staining was observed in the nucleus reuniens, dorsal thalamus and amygdala, but not in the neocortex, hippocampus or piriform/endopiriform area. Panel (B) : FJB severity scores by region in the 3 experimental groups. Neuronal FJB staining was most extensive in neocortex and central thalamus, and was lowest in the hippocampus. Small numbers of FJB stained neurons in the ILE-treated group were only observed in the dorsal and central thalamus and the amygdala, but no neuronal FJB staining was observed in the other 3 regions. Error bars in panel B indicate standard deviation for the inter-animal FJB-staining variability in each brain region. One-way ANOVA on ranks indicated all POX + ISO neuropathology scores were significantly different from the scores in untreated animals (P < 0.002).
Tissue Sectioning And Fjb Staining, supplied by FD NeuroTechnologies, 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/fj-b+staining+fj-b/tissue+sectioning+and+fjb+staining/pmc11479933-47-3-8
Average 90 stars, based on 1 article reviews
tissue sectioning and fjb staining - by Bioz Stars, 2026-09
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86
Servicebio Inc fluoro jade b staining kit
Neuropathology as determined <t>by</t> <t>FJB-staining.</t> Animal groups included injured (POX = paraoxon, n = 7), treated (paraoxon plus ILE given 30 min later, n = 8) and naïve control (cannula implantation, but no other treatment, n = 5). Panel (A) : FJB severity scores in each animal in the study. Error bars show the standard deviation in each brain area among the tissue sections for each animal. Results for each animal are based on observations in 14–20 tissue sections (some areas, including the nucleus reuniens, are only visible in a limited rostro-caudal extent and so fewer tissue sections contribute to the neuropathology score). Animal identification numbers and experimental groups are shown on the X-axis, and FJB scores (from 0–10) are given on the Y-axis. In the ILE-treated rats, very minor FJB staining was observed in the nucleus reuniens, dorsal thalamus and amygdala, but not in the neocortex, hippocampus or piriform/endopiriform area. Panel (B) : FJB severity scores by region in the 3 experimental groups. Neuronal FJB staining was most extensive in neocortex and central thalamus, and was lowest in the hippocampus. Small numbers of FJB stained neurons in the ILE-treated group were only observed in the dorsal and central thalamus and the amygdala, but no neuronal FJB staining was observed in the other 3 regions. Error bars in panel B indicate standard deviation for the inter-animal FJB-staining variability in each brain region. One-way ANOVA on ranks indicated all POX + ISO neuropathology scores were significantly different from the scores in untreated animals (P < 0.002).
Fluoro Jade B Staining Kit, supplied by Servicebio Inc, 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/fj-b+staining+fj-b/b+fjb+fluoro+jade+staining/10__1016_slash_j__fbio__2025__105859-58-0-7
Average 86 stars, based on 1 article reviews
fluoro jade b staining kit - by Bioz Stars, 2026-09
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95
Antibodies Inc fluoro-jade b (fjb) staining kit
Neuropathology as determined <t>by</t> <t>FJB-staining.</t> Animal groups included injured (POX = paraoxon, n = 7), treated (paraoxon plus ILE given 30 min later, n = 8) and naïve control (cannula implantation, but no other treatment, n = 5). Panel (A) : FJB severity scores in each animal in the study. Error bars show the standard deviation in each brain area among the tissue sections for each animal. Results for each animal are based on observations in 14–20 tissue sections (some areas, including the nucleus reuniens, are only visible in a limited rostro-caudal extent and so fewer tissue sections contribute to the neuropathology score). Animal identification numbers and experimental groups are shown on the X-axis, and FJB scores (from 0–10) are given on the Y-axis. In the ILE-treated rats, very minor FJB staining was observed in the nucleus reuniens, dorsal thalamus and amygdala, but not in the neocortex, hippocampus or piriform/endopiriform area. Panel (B) : FJB severity scores by region in the 3 experimental groups. Neuronal FJB staining was most extensive in neocortex and central thalamus, and was lowest in the hippocampus. Small numbers of FJB stained neurons in the ILE-treated group were only observed in the dorsal and central thalamus and the amygdala, but no neuronal FJB staining was observed in the other 3 regions. Error bars in panel B indicate standard deviation for the inter-animal FJB-staining variability in each brain region. One-way ANOVA on ranks indicated all POX + ISO neuropathology scores were significantly different from the scores in untreated animals (P < 0.002).
Fluoro Jade B (Fjb) Staining Kit, supplied by Antibodies Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fj-b+staining+fj-b/Fluoro-Jade+B+(FJB)+Staining+Kit/custom%40tr-150-fjb%4039972331
Average 95 stars, based on 1 article reviews
fluoro-jade b (fjb) staining kit - by Bioz Stars, 2026-09
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Image Search Results


Neuropathology as determined by FJB-staining. Animal groups included injured (POX = paraoxon, n = 7), treated (paraoxon plus ILE given 30 min later, n = 8) and naïve control (cannula implantation, but no other treatment, n = 5). Panel (A) : FJB severity scores in each animal in the study. Error bars show the standard deviation in each brain area among the tissue sections for each animal. Results for each animal are based on observations in 14–20 tissue sections (some areas, including the nucleus reuniens, are only visible in a limited rostro-caudal extent and so fewer tissue sections contribute to the neuropathology score). Animal identification numbers and experimental groups are shown on the X-axis, and FJB scores (from 0–10) are given on the Y-axis. In the ILE-treated rats, very minor FJB staining was observed in the nucleus reuniens, dorsal thalamus and amygdala, but not in the neocortex, hippocampus or piriform/endopiriform area. Panel (B) : FJB severity scores by region in the 3 experimental groups. Neuronal FJB staining was most extensive in neocortex and central thalamus, and was lowest in the hippocampus. Small numbers of FJB stained neurons in the ILE-treated group were only observed in the dorsal and central thalamus and the amygdala, but no neuronal FJB staining was observed in the other 3 regions. Error bars in panel B indicate standard deviation for the inter-animal FJB-staining variability in each brain region. One-way ANOVA on ranks indicated all POX + ISO neuropathology scores were significantly different from the scores in untreated animals (P < 0.002).

Journal: Frontiers in Pharmacology

Article Title: Isoflurane-lipid emulsion injection as an anticonvulsant and neuroprotectant treatment for nerve agent exposure

doi: 10.3389/fphar.2024.1466351

Figure Lengend Snippet: Neuropathology as determined by FJB-staining. Animal groups included injured (POX = paraoxon, n = 7), treated (paraoxon plus ILE given 30 min later, n = 8) and naïve control (cannula implantation, but no other treatment, n = 5). Panel (A) : FJB severity scores in each animal in the study. Error bars show the standard deviation in each brain area among the tissue sections for each animal. Results for each animal are based on observations in 14–20 tissue sections (some areas, including the nucleus reuniens, are only visible in a limited rostro-caudal extent and so fewer tissue sections contribute to the neuropathology score). Animal identification numbers and experimental groups are shown on the X-axis, and FJB scores (from 0–10) are given on the Y-axis. In the ILE-treated rats, very minor FJB staining was observed in the nucleus reuniens, dorsal thalamus and amygdala, but not in the neocortex, hippocampus or piriform/endopiriform area. Panel (B) : FJB severity scores by region in the 3 experimental groups. Neuronal FJB staining was most extensive in neocortex and central thalamus, and was lowest in the hippocampus. Small numbers of FJB stained neurons in the ILE-treated group were only observed in the dorsal and central thalamus and the amygdala, but no neuronal FJB staining was observed in the other 3 regions. Error bars in panel B indicate standard deviation for the inter-animal FJB-staining variability in each brain region. One-way ANOVA on ranks indicated all POX + ISO neuropathology scores were significantly different from the scores in untreated animals (P < 0.002).

Article Snippet: Tissue sectioning and FJB staining were done by FD Neurotechnologies (Columbia, MD).

Techniques: Staining, Control, Standard Deviation

FJB staining in neocortex and the central thalamus including the nucleus reuniens. Neocortex was a major site of POX-induced neuronal damage as shown by FJB staining (left panels; cc = corpus callosum). FJB staining in cortex was variable in the animals not treated with ILE, ranging from no FJB staining in one animal to very extensive neuronal damage in the other 6 animals (see ). No FJB staining was observed in the neocortex of any of the animals treated with the ILE (see ). In the central thalamus, including the nucleus reuniens, FJB staining was moderate to strong in all of the animals not treated with the ILE (right panels; III = third ventricle). Very low FJB staining was observed in the nucleus reuniens from all of the rats treated with the ILE (bottom right panel).

Journal: Frontiers in Pharmacology

Article Title: Isoflurane-lipid emulsion injection as an anticonvulsant and neuroprotectant treatment for nerve agent exposure

doi: 10.3389/fphar.2024.1466351

Figure Lengend Snippet: FJB staining in neocortex and the central thalamus including the nucleus reuniens. Neocortex was a major site of POX-induced neuronal damage as shown by FJB staining (left panels; cc = corpus callosum). FJB staining in cortex was variable in the animals not treated with ILE, ranging from no FJB staining in one animal to very extensive neuronal damage in the other 6 animals (see ). No FJB staining was observed in the neocortex of any of the animals treated with the ILE (see ). In the central thalamus, including the nucleus reuniens, FJB staining was moderate to strong in all of the animals not treated with the ILE (right panels; III = third ventricle). Very low FJB staining was observed in the nucleus reuniens from all of the rats treated with the ILE (bottom right panel).

Article Snippet: Tissue sectioning and FJB staining were done by FD Neurotechnologies (Columbia, MD).

Techniques: Staining

FJB staining in the hippocampus and dorsal thalamus. In our POX model, neuronal FJB staining was relatively less extensive in the hippocampus than in regions such as neocortex and central thalamus (left panels; also see ; cc = corpus callosum). Neuronal FJB staining was observed in pyramidal cells in CA1, CA2 and CA3, as well as in neurons in the polymorph layer. No neuronal FJB staining was observed in the hippocampus of any of the ILE-treated animals. The dorsal thalamus was another site of extensive neuronal FJB staining in the animals given POX but not treated with the ILE (center right panel; sm = stria medularis). Very minimal neuronal FJB staining was observed in the dorsal thalamus of all of the ILE-treated animals (bottom right panel, also see ).

Journal: Frontiers in Pharmacology

Article Title: Isoflurane-lipid emulsion injection as an anticonvulsant and neuroprotectant treatment for nerve agent exposure

doi: 10.3389/fphar.2024.1466351

Figure Lengend Snippet: FJB staining in the hippocampus and dorsal thalamus. In our POX model, neuronal FJB staining was relatively less extensive in the hippocampus than in regions such as neocortex and central thalamus (left panels; also see ; cc = corpus callosum). Neuronal FJB staining was observed in pyramidal cells in CA1, CA2 and CA3, as well as in neurons in the polymorph layer. No neuronal FJB staining was observed in the hippocampus of any of the ILE-treated animals. The dorsal thalamus was another site of extensive neuronal FJB staining in the animals given POX but not treated with the ILE (center right panel; sm = stria medularis). Very minimal neuronal FJB staining was observed in the dorsal thalamus of all of the ILE-treated animals (bottom right panel, also see ).

Article Snippet: Tissue sectioning and FJB staining were done by FD Neurotechnologies (Columbia, MD).

Techniques: Staining

FJB staining in the amygdala complex and piriform cortex/endopiriform area. The amygdala was one of the regions with moderate to strong neuronal FJB-staining (left panels; ot = optic tract). Only one out of 8 of the ILE-treated animals had residual neuronal FJB staining, whereas no stained neurons were observed in the other 7 animals (see ). Neuronal FJB staining was moderate to strong in the POX group (center right panel; CP = caudate/putamen), but no neuronal FJB staining was observed in the POX + ISO group (bottom right panel).

Journal: Frontiers in Pharmacology

Article Title: Isoflurane-lipid emulsion injection as an anticonvulsant and neuroprotectant treatment for nerve agent exposure

doi: 10.3389/fphar.2024.1466351

Figure Lengend Snippet: FJB staining in the amygdala complex and piriform cortex/endopiriform area. The amygdala was one of the regions with moderate to strong neuronal FJB-staining (left panels; ot = optic tract). Only one out of 8 of the ILE-treated animals had residual neuronal FJB staining, whereas no stained neurons were observed in the other 7 animals (see ). Neuronal FJB staining was moderate to strong in the POX group (center right panel; CP = caudate/putamen), but no neuronal FJB staining was observed in the POX + ISO group (bottom right panel).

Article Snippet: Tissue sectioning and FJB staining were done by FD Neurotechnologies (Columbia, MD).

Techniques: Staining