compound 97 against s aureus atcc Search Results


hairpin ribozyme genes  (Immusol Inc)
90
Immusol Inc hairpin ribozyme genes
Hairpin Ribozyme Genes, supplied by Immusol 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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antibodies against golga1 1 golgin 97  (Atlas Antibodies)
92
Atlas Antibodies antibodies against golga1 1 golgin 97
Antibodies Against Golga1 1 Golgin 97, supplied by Atlas Antibodies, 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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chicken protein database  (Gallus BioPharmaceuticals)
90
Gallus BioPharmaceuticals chicken protein database
Chicken Protein Database, supplied by Gallus BioPharmaceuticals, 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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mouse monoclonal igg against neurofilaments  (Bio-Rad)
93
Bio-Rad mouse monoclonal igg against neurofilaments
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
Mouse Monoclonal Igg Against Neurofilaments, supplied by Bio-Rad, 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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antibodies against trim3  (Boster Bio)
90
Boster Bio antibodies against trim3
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
Antibodies Against Trim3, supplied by Boster Bio, 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
antibodies against trim3 - by Bioz Stars, 2026-09
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s aureus atcc  (ATCC)
99
ATCC s aureus atcc
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
S Aureus Atcc, supplied by ATCC, 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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Average 99 stars, based on 1 article reviews
s aureus atcc - by Bioz Stars, 2026-09
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golgin  (Santa Cruz Biotechnology)
94
Santa Cruz Biotechnology golgin
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
Golgin, supplied by Santa Cruz Biotechnology, 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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golgin - by Bioz Stars, 2026-09
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venti database  (CoreBiome Inc)
90
CoreBiome Inc venti database
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
Venti Database, supplied by CoreBiome 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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Average 90 stars, based on 1 article reviews
venti database - by Bioz Stars, 2026-09
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inhibition against s aureus atcc 25923  (ATCC)
99
ATCC inhibition against s aureus atcc 25923
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
Inhibition Against S Aureus Atcc 25923, supplied by ATCC, 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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inhibition against s aureus atcc 25923 - by Bioz Stars, 2026-09
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pseudomonas aeruginosa 97 09  (ATCC)
99
ATCC pseudomonas aeruginosa 97 09
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
Pseudomonas Aeruginosa 97 09, supplied by ATCC, 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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rabbit mab against mouse cd11c  (Cell Signaling Technology Inc)
94
Cell Signaling Technology Inc rabbit mab against mouse cd11c
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
Rabbit Mab Against Mouse Cd11c, supplied by Cell Signaling Technology Inc, 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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silva reference database  (Vishuo Biomedical Pte Ltd)
90
Vishuo Biomedical Pte Ltd silva reference database
Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), <t>neurofilament</t> (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.
Silva Reference Database, supplied by Vishuo Biomedical Pte Ltd, 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


Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), neurofilament (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.

Journal: The Journal of Neuroscience

Article Title: Long-Distance Axonal Regeneration in the Transected Adult Rat Spinal Cord Is Promoted by Olfactory Ensheathing Glia Transplants

doi: 10.1523/JNEUROSCI.18-10-03803.1998

Figure Lengend Snippet: Regenerating axons crossing the gliotic tissue created at both graft–cord interfaces after EG transplantation.A–E, Consecutive spinal cord sagittal sections showing the interfaces between the rostral cord stump and either SC and EG cables or EG connective tissue bridges. Sections were immunolabeled for GFAP (A), ED1 (B), neurofilament (D), and GAP-43 (E). EG were visualized by Hoechst labeling (C). A portion of the channel, which autofluoresces with the filter used, was retained in C(asterisk). Arrowheads inA, B, D, andE point to the cord–cable interface;arrows in A–E mark the EG-containing connective tissue bridge.F–H, Consecutive spinal cord sections showing the caudal cord–cable interface. Dashed lines(F, G) indicate the interface. Sections were immunolabeled for GFAP (F) and GAP-43 (G). Hoechst-labeled EG (H) are in the same region shown inF. Arrows in G point to GAP-43-labeled fibers crossing the cord–cable interface and in the gliotic tissue. Note the presence of EG in the gliotic tissue of both interfaces (C, H) and in both SC-containing cables and connective tissue bridges (C). Scale bars:A–E, 125 μm;F–H, 90 μm.

Article Snippet: We also used mouse monoclonal IgG against neurofilaments (RT-97; Developmental Hybridoma Bank) (1:5) and anti-ED1 (Serotec, Indianapolis, IN), a mouse monoclonal IgG (1:200).

Techniques: Transplantation Assay, Immunolabeling, Labeling