p jnk Search Results


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R&D Systems phosphor jnk1 2 thr183 tyr185
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Chem Impex International compound 1
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Santa Cruz Biotechnology phosphorylated jnk
Figure 4. Immunohistochemistry of <t>phosphorylated</t> <t>JNK</t> in cultured hippocampal neurons. a, Neurons were identified by antibodies directed against the axonal marker protein tau (green). Only rare punctate staining of <t>phosphorylated</t> <t>JNK</t> (red) was detected in untreated neurons. Scale bar, 10 m. b, Phosphorylated JNK (red) was observed in most tau (green)-positive axons after treatment of the cultures with 300 M DEA/NONOate for 5 min. Area selected for inset as indicated. Scale bar, 10 m. c, Percentageofaxonsidentifiedbyimmunolabelingwithantibodiesdirectedagainsttauthatshowdouble-labelingforphosphor- ylatedJNK.Neuronsareeitheruntreatedortreatedwith300MDEA/NONOatefor5,10,or15min.Dataarepresentedasmean SEM. **p 0.005.
Phosphorylated Jnk, supplied by Santa Cruz Biotechnology, 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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Promega anti-p-jnk (ptppy)
Figure 4. Immunohistochemistry of <t>phosphorylated</t> <t>JNK</t> in cultured hippocampal neurons. a, Neurons were identified by antibodies directed against the axonal marker protein tau (green). Only rare punctate staining of <t>phosphorylated</t> <t>JNK</t> (red) was detected in untreated neurons. Scale bar, 10 m. b, Phosphorylated JNK (red) was observed in most tau (green)-positive axons after treatment of the cultures with 300 M DEA/NONOate for 5 min. Area selected for inset as indicated. Scale bar, 10 m. c, Percentageofaxonsidentifiedbyimmunolabelingwithantibodiesdirectedagainsttauthatshowdouble-labelingforphosphor- ylatedJNK.Neuronsareeitheruntreatedortreatedwith300MDEA/NONOatefor5,10,or15min.Dataarepresentedasmean SEM. **p 0.005.
Anti P Jnk (Ptppy), supplied by Promega, 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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Affinity Biosciences p-jnk (1:1000; #af3318:ab_2834737)
Figure 4. Immunohistochemistry of <t>phosphorylated</t> <t>JNK</t> in cultured hippocampal neurons. a, Neurons were identified by antibodies directed against the axonal marker protein tau (green). Only rare punctate staining of <t>phosphorylated</t> <t>JNK</t> (red) was detected in untreated neurons. Scale bar, 10 m. b, Phosphorylated JNK (red) was observed in most tau (green)-positive axons after treatment of the cultures with 300 M DEA/NONOate for 5 min. Area selected for inset as indicated. Scale bar, 10 m. c, Percentageofaxonsidentifiedbyimmunolabelingwithantibodiesdirectedagainsttauthatshowdouble-labelingforphosphor- ylatedJNK.Neuronsareeitheruntreatedortreatedwith300MDEA/NONOatefor5,10,or15min.Dataarepresentedasmean SEM. **p 0.005.
P Jnk (1:1000; #Af3318:Ab 2834737), supplied by Affinity Biosciences, 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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Servicebio Inc rabbit anti-p-jnk
Figure 4. Immunohistochemistry of <t>phosphorylated</t> <t>JNK</t> in cultured hippocampal neurons. a, Neurons were identified by antibodies directed against the axonal marker protein tau (green). Only rare punctate staining of <t>phosphorylated</t> <t>JNK</t> (red) was detected in untreated neurons. Scale bar, 10 m. b, Phosphorylated JNK (red) was observed in most tau (green)-positive axons after treatment of the cultures with 300 M DEA/NONOate for 5 min. Area selected for inset as indicated. Scale bar, 10 m. c, Percentageofaxonsidentifiedbyimmunolabelingwithantibodiesdirectedagainsttauthatshowdouble-labelingforphosphor- ylatedJNK.Neuronsareeitheruntreatedortreatedwith300MDEA/NONOatefor5,10,or15min.Dataarepresentedasmean SEM. **p 0.005.
Rabbit Anti P Jnk, supplied by Servicebio 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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Huabio Inc primary antibodies against p-jnk
Figure 4. Immunohistochemistry of <t>phosphorylated</t> <t>JNK</t> in cultured hippocampal neurons. a, Neurons were identified by antibodies directed against the axonal marker protein tau (green). Only rare punctate staining of <t>phosphorylated</t> <t>JNK</t> (red) was detected in untreated neurons. Scale bar, 10 m. b, Phosphorylated JNK (red) was observed in most tau (green)-positive axons after treatment of the cultures with 300 M DEA/NONOate for 5 min. Area selected for inset as indicated. Scale bar, 10 m. c, Percentageofaxonsidentifiedbyimmunolabelingwithantibodiesdirectedagainsttauthatshowdouble-labelingforphosphor- ylatedJNK.Neuronsareeitheruntreatedortreatedwith300MDEA/NONOatefor5,10,or15min.Dataarepresentedasmean SEM. **p 0.005.
Primary Antibodies Against P Jnk, supplied by Huabio 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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ABclonal Biotechnology rabbit anti-mouse antibodies against jnk
Licorice zinc inhibited UVB-induced <t>JNK/P38MAPK</t> signaling pathway activation. C57BL/6J mice skin was treated with UVB, mice were given licorice zinc (0.65 g/kg, 1.3 g/kg, 2.6 g/kg) and 250mg tranexamic acid once a day. (a) JNK/ P38MAPK signaling pathway-related proteins were analyzed by western blotting <t>using</t> <t>antibodies</t> against JNK, p-JNK, P38MAPK, and p-P38MAPK, β-actin served as a loading control. (b) The ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.
Rabbit Anti Mouse Antibodies Against Jnk, supplied by ABclonal Biotechnology, 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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ABclonal Biotechnology anti-p-jnk
Licorice zinc inhibited UVB-induced <t>JNK/P38MAPK</t> signaling pathway activation. C57BL/6J mice skin was treated with UVB, mice were given licorice zinc (0.65 g/kg, 1.3 g/kg, 2.6 g/kg) and 250mg tranexamic acid once a day. (a) JNK/ P38MAPK signaling pathway-related proteins were analyzed by western blotting <t>using</t> <t>antibodies</t> against JNK, p-JNK, P38MAPK, and p-P38MAPK, β-actin served as a loading control. (b) The ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.
Anti P Jnk, supplied by ABclonal Biotechnology, 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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Beyotime primary antibodies against β-actin, p50, p65, erk, p-erk, jnk p-jnk, p38
Licorice zinc inhibited UVB-induced <t>JNK/P38MAPK</t> signaling pathway activation. C57BL/6J mice skin was treated with UVB, mice were given licorice zinc (0.65 g/kg, 1.3 g/kg, 2.6 g/kg) and 250mg tranexamic acid once a day. (a) JNK/ P38MAPK signaling pathway-related proteins were analyzed by western blotting <t>using</t> <t>antibodies</t> against JNK, p-JNK, P38MAPK, and p-P38MAPK, β-actin served as a loading control. (b) The ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.
Primary Antibodies Against β Actin, P50, P65, Erk, P Erk, Jnk P Jnk, P38, supplied by Beyotime, 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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Abmart Inc antibody p-jnk ta3318
Licorice zinc inhibited UVB-induced <t>JNK/P38MAPK</t> signaling pathway activation. C57BL/6J mice skin was treated with UVB, mice were given licorice zinc (0.65 g/kg, 1.3 g/kg, 2.6 g/kg) and 250mg tranexamic acid once a day. (a) JNK/ P38MAPK signaling pathway-related proteins were analyzed by western blotting <t>using</t> <t>antibodies</t> against JNK, p-JNK, P38MAPK, and p-P38MAPK, β-actin served as a loading control. (b) The ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.
Antibody P Jnk Ta3318, supplied by Abmart 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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Becton Dickinson anti-p-jnk antibody 7170701
Licorice zinc inhibited UVB-induced <t>JNK/P38MAPK</t> signaling pathway activation. C57BL/6J mice skin was treated with UVB, mice were given licorice zinc (0.65 g/kg, 1.3 g/kg, 2.6 g/kg) and 250mg tranexamic acid once a day. (a) JNK/ P38MAPK signaling pathway-related proteins were analyzed by western blotting <t>using</t> <t>antibodies</t> against JNK, p-JNK, P38MAPK, and p-P38MAPK, β-actin served as a loading control. (b) The ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.
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Image Search Results


Figure 4. Immunohistochemistry of phosphorylated JNK in cultured hippocampal neurons. a, Neurons were identified by antibodies directed against the axonal marker protein tau (green). Only rare punctate staining of phosphorylated JNK (red) was detected in untreated neurons. Scale bar, 10 m. b, Phosphorylated JNK (red) was observed in most tau (green)-positive axons after treatment of the cultures with 300 M DEA/NONOate for 5 min. Area selected for inset as indicated. Scale bar, 10 m. c, Percentageofaxonsidentifiedbyimmunolabelingwithantibodiesdirectedagainsttauthatshowdouble-labelingforphosphor- ylatedJNK.Neuronsareeitheruntreatedortreatedwith300MDEA/NONOatefor5,10,or15min.Dataarepresentedasmean SEM. **p 0.005.

Journal: Journal of Neuroscience

Article Title: Breakdown of Axonal Synaptic Vesicle Precursor Transport by Microglial Nitric Oxide

doi: 10.1523/jneurosci.3887-04.2005

Figure Lengend Snippet: Figure 4. Immunohistochemistry of phosphorylated JNK in cultured hippocampal neurons. a, Neurons were identified by antibodies directed against the axonal marker protein tau (green). Only rare punctate staining of phosphorylated JNK (red) was detected in untreated neurons. Scale bar, 10 m. b, Phosphorylated JNK (red) was observed in most tau (green)-positive axons after treatment of the cultures with 300 M DEA/NONOate for 5 min. Area selected for inset as indicated. Scale bar, 10 m. c, Percentageofaxonsidentifiedbyimmunolabelingwithantibodiesdirectedagainsttauthatshowdouble-labelingforphosphor- ylatedJNK.Neuronsareeitheruntreatedortreatedwith300MDEA/NONOatefor5,10,or15min.Dataarepresentedasmean SEM. **p 0.005.

Article Snippet: Hippocampal neurons cultured for 1 week were fixed with 4% paraformaldehyde, incubated with a mouse monoclonal antibody specific for phosphorylated JNK (2 g/ml; Santa Cruz Biotechnology, Santa Cruz, CA), followed by secondary fluorochrome Cy3-conjugated goat antibody directed against mouse IgG (2 g/ml; Dianova).

Techniques: Immunohistochemistry, Cell Culture, Marker, Staining

Licorice zinc inhibited UVB-induced JNK/P38MAPK signaling pathway activation. C57BL/6J mice skin was treated with UVB, mice were given licorice zinc (0.65 g/kg, 1.3 g/kg, 2.6 g/kg) and 250mg tranexamic acid once a day. (a) JNK/ P38MAPK signaling pathway-related proteins were analyzed by western blotting using antibodies against JNK, p-JNK, P38MAPK, and p-P38MAPK, β-actin served as a loading control. (b) The ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.

Journal: Acta Cirúrgica Brasileira

Article Title: Licorice zinc suppresses melanogenesis via inhibiting the activation of P38MAPK and JNK signaling pathway in C57BL/6J mice skin

doi: 10.1590/acb371002

Figure Lengend Snippet: Licorice zinc inhibited UVB-induced JNK/P38MAPK signaling pathway activation. C57BL/6J mice skin was treated with UVB, mice were given licorice zinc (0.65 g/kg, 1.3 g/kg, 2.6 g/kg) and 250mg tranexamic acid once a day. (a) JNK/ P38MAPK signaling pathway-related proteins were analyzed by western blotting using antibodies against JNK, p-JNK, P38MAPK, and p-P38MAPK, β-actin served as a loading control. (b) The ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.

Article Snippet: Then, probed with rabbit anti-mouse antibodies against JNK (1:1,000, abclonal, no. A5051, Wuhan, China), p-JNK (1:1,000, abclonal, no. Ap0276, Wuhan, China), P38MAPK (1:800, abclonal, no. A14401, Wuhan, China), p-P38MAPK (1:1,000, abclonal, no. Ap0526, Wuhan, China), TRP-1 (1:1,000, abclonal, no. A4016, Wuhan, China), tyrosinase (1:1,000, abclonal, no. A1254, Wuhan, China), MITF (1:1,000, abclonal, no. A11649, Wuhan, China), and β-actin (1:100,000, abclonal, no. AC026, Wuhan, China) at 4 °C overnight.

Techniques: Activation Assay, Western Blot

Inhibition JNK pathway restrained UVB--induced melanin formation. After B16F10 cells were cultured for 24 h, cells were treated with 0.1 mM α-MSH for 72 h, meanwhile, cells were treated with licorice zinc negative serum, 10% licorice zinc positive serum, and 10% licorice zinc positive serum+Anisomycin. The Control group was cultured with nothing except medium all along. (a) The content of melanin was measured by sodium hydroxide dissolution. (b) JNK/ P38MAPK signaling pathway and melanin productionrelated protein were an alyzed by western blotting using antibodies against JNK, p-JNK, P38MAPK, pP38MAPK, TRP-1, tyrosinase, and MTIF. β-actin served as a loading control. (c) The relative density of TRP1, tyrosinase, and MTIF, and the ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.

Journal: Acta Cirúrgica Brasileira

Article Title: Licorice zinc suppresses melanogenesis via inhibiting the activation of P38MAPK and JNK signaling pathway in C57BL/6J mice skin

doi: 10.1590/acb371002

Figure Lengend Snippet: Inhibition JNK pathway restrained UVB--induced melanin formation. After B16F10 cells were cultured for 24 h, cells were treated with 0.1 mM α-MSH for 72 h, meanwhile, cells were treated with licorice zinc negative serum, 10% licorice zinc positive serum, and 10% licorice zinc positive serum+Anisomycin. The Control group was cultured with nothing except medium all along. (a) The content of melanin was measured by sodium hydroxide dissolution. (b) JNK/ P38MAPK signaling pathway and melanin productionrelated protein were an alyzed by western blotting using antibodies against JNK, p-JNK, P38MAPK, pP38MAPK, TRP-1, tyrosinase, and MTIF. β-actin served as a loading control. (c) The relative density of TRP1, tyrosinase, and MTIF, and the ratio of p-JNK/ JNK and p-P38MAPK/ P38MAPK were quantified by western blotting analysis and normalized to control.

Article Snippet: Then, probed with rabbit anti-mouse antibodies against JNK (1:1,000, abclonal, no. A5051, Wuhan, China), p-JNK (1:1,000, abclonal, no. Ap0276, Wuhan, China), P38MAPK (1:800, abclonal, no. A14401, Wuhan, China), p-P38MAPK (1:1,000, abclonal, no. Ap0526, Wuhan, China), TRP-1 (1:1,000, abclonal, no. A4016, Wuhan, China), tyrosinase (1:1,000, abclonal, no. A1254, Wuhan, China), MITF (1:1,000, abclonal, no. A11649, Wuhan, China), and β-actin (1:100,000, abclonal, no. AC026, Wuhan, China) at 4 °C overnight.

Techniques: Inhibition, Cell Culture, Western Blot