rabbit anti-p65 Search Results


90
Leinco Technologies rabbit anti-p65
(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and <t>p-p65</t> was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.
Rabbit Anti P65, supplied by Leinco Technologies, 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/result/rabbit anti-p65/product/Leinco Technologies
Average 90 stars, based on 1 article reviews
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90
Wanleibio p65 antibody
(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and <t>p-p65</t> was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.
P65 Antibody, supplied by Wanleibio, 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
p65 antibody - by Bioz Stars, 2026-03
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90
Elabscience Biotechnology rabbit anti-p65 eap1020
(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and <t>p-p65</t> was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.
Rabbit Anti P65 Eap1020, supplied by Elabscience Biotechnology, 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/result/rabbit anti-p65 eap1020/product/Elabscience Biotechnology
Average 90 stars, based on 1 article reviews
rabbit anti-p65 eap1020 - by Bioz Stars, 2026-03
90/100 stars
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90
Active Motif rabbit anti-p65/nf-κb antibody
(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and <t>p-p65</t> was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.
Rabbit Anti P65/Nf κb Antibody, supplied by Active Motif, 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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90
Bioworld Antibodies anti-p65 (bs3157, rabbit-pab
(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and <t>p-p65</t> was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.
Anti P65 (Bs3157, Rabbit Pab, supplied by Bioworld Antibodies, 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/result/anti-p65 (bs3157, rabbit-pab/product/Bioworld Antibodies
Average 90 stars, based on 1 article reviews
anti-p65 (bs3157, rabbit-pab - by Bioz Stars, 2026-03
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90
Cedarlane rabbit anti-p65 nf-jb antibody
(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and <t>p-p65</t> was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.
Rabbit Anti P65 Nf Jb Antibody, supplied by Cedarlane, 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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90
Autogen-Bioclear ltd rabbit anti-p65
(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and <t>p-p65</t> was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.
Rabbit Anti P65, supplied by Autogen-Bioclear ltd, 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/result/rabbit anti-p65/product/Autogen-Bioclear ltd
Average 90 stars, based on 1 article reviews
rabbit anti-p65 - by Bioz Stars, 2026-03
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90
Bio Basic Canada rabbit anti-p65 (rela)
(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and <t>p-p65</t> was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.
Rabbit Anti P65 (Rela), supplied by Bio Basic Canada, 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


(A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and p-p65 was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.

Journal: PLoS ONE

Article Title: β5 Integrin Up-Regulation in Brain-Derived Neurotrophic Factor Promotes Cell Motility in Human Chondrosarcoma

doi: 10.1371/journal.pone.0067990

Figure Lengend Snippet: (A) Cells were pretreated for 30 min with PDTC (10 µM) and TPCK (3 µM) or transfected with dominant negative (DN) mutants of IKKα or IKKβ for 24 h, and then allowed to migrate for 24 h toward BDNF (50 ng/ml)-containing medium. In vitro migration was examined using a Transwell assay (n = 5). (B&C) Cells were pretreated for 30 min with PDTC and TPCK or transfected with IKKα or IKKβ mutants for 24 h, followed by stimulation with BDNF. The mRNA and cell-surface β5 integrin expression was examined using qPCR and flow cytometry (n = 4). (D) Cells were incubated with BDNF for the indicated time intervals, and p-IKK, p-IκBα, and p-p65 was examined by western blotting (n = 5). (E) Cells were pretreated for 30 min with Ly294002, wortmannin, and Akt inhibitor, followed by stimulation with BDNF, and p-p65 expression was examined by western blotting (n = 4). Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.

Article Snippet: The cells were then incubated with rabbit anti-p65 (1∶100) and FITC-conjugated goat anti-rabbit secondary antibody (1∶100; Leinco Technologies Inc) for 1 h. Finally, cells stained with DAPI for 5 min were washed, mounted, and examined with a Zeiss fluorescence microscope.

Techniques: Transfection, Dominant Negative Mutation, In Vitro, Migration, Transwell Assay, Expressing, Flow Cytometry, Incubation, Western Blot, Control

(A&B) Cells were pretreated with Ly294002, wortmannin, Akt inhibitor, PDTC, and TPCK for 30 min or transfected with mutants of p85, Akt, IKKα, and IKKβ before exposure to BDNF. NF-κB luciferase activity was measured, and the results were normalized to β-galactosidase activity and expressed as the mean ± SEM. for 3 independent experiments performed in triplicate (n = 5). (C) Cells were pretreated with Ly294002, wortmannin, and Akt inhibitor for 30 min then stimulated with BDNF for 60 min, and p65 immunofluorescence staining was examined (n = 4). Size bar = 20 µm. Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.

Journal: PLoS ONE

Article Title: β5 Integrin Up-Regulation in Brain-Derived Neurotrophic Factor Promotes Cell Motility in Human Chondrosarcoma

doi: 10.1371/journal.pone.0067990

Figure Lengend Snippet: (A&B) Cells were pretreated with Ly294002, wortmannin, Akt inhibitor, PDTC, and TPCK for 30 min or transfected with mutants of p85, Akt, IKKα, and IKKβ before exposure to BDNF. NF-κB luciferase activity was measured, and the results were normalized to β-galactosidase activity and expressed as the mean ± SEM. for 3 independent experiments performed in triplicate (n = 5). (C) Cells were pretreated with Ly294002, wortmannin, and Akt inhibitor for 30 min then stimulated with BDNF for 60 min, and p65 immunofluorescence staining was examined (n = 4). Size bar = 20 µm. Results are expressed as the mean ± SEM. *, p <0.05 compared with the control. # , p <0.05 compared with the BDNF-treated group.

Article Snippet: The cells were then incubated with rabbit anti-p65 (1∶100) and FITC-conjugated goat anti-rabbit secondary antibody (1∶100; Leinco Technologies Inc) for 1 h. Finally, cells stained with DAPI for 5 min were washed, mounted, and examined with a Zeiss fluorescence microscope.

Techniques: Transfection, Luciferase, Activity Assay, Immunofluorescence, Staining, Control