180 elisa kits Search Results


94
Cell Signaling Technology Inc p p38 mapk thr180 tyr182
HMJ-30 inhibits the Ras/MAPK, PI3K/AKT, and NF-κB signaling pathways in human osteogenic sarcoma U-2 OS cells. (A) Protein levels of Ras, p-ERK, p-JNK and <t>p-p38</t> were downregulated, as determined by western blotting. Expression of the key proteins in MAPK signaling, (B) p-ERK (p-p44/42) and (C) p-p38, were reconfirmed using ELISA assays. (D) The protein levels of PI3K (p85) and p-AKT were downregulated, as determined by western blot-ting. (E) The key protein in p-AKT was reconfirmed by ELISA assay. (F) Protein levels of IKK, p-IκB and NF-κB (p65) were downregulated, as determined by western blotting. (G) NF-κB binding activity was determined using an electrophoretic mobility shift assay. Inhibitors of p44/22 MAPK (U0126), p38 (SB203580), PI3K (wortmannin) and NF-κB (PDTC), as positive controls, reduced protein kinase levels. The data represents the mean ± standard deviation of three experiments. *** P<0.001 vs. control. HMJ-30, 6-fluoro-2-(3-fluorophenyl)-4-(cyanoanilino)quinazoline; MAPK, mitogen-activated protein kinase; PI3K, phosphoinositide 3-kinase; AKT, protein kinase B; NF-κB, nuclear factor-κB; p-, phosphorylated; ERK, extracelullar signal-regulated kinase; JNK, c-Jun amino-terminal kinase; PDTC, ammonium pyrrolidinedithiocarbamate.
P P38 Mapk Thr180 Tyr182, 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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Cell Signaling Technology Inc pathscan phospho ikkα
A. Co-immunoprecipitation assay showing NEMO is essential for mediating the interaction of K13 with IKK1 and IKK2. FLAG-tagged K13 was immunoprecipitated from WT and NEMO-deficient Jurkat cells using control (C) and FLAG (F) antibody beads and presence of co-immunoprecipitated IKK1, IKK2 and NEMO detected by immunoblotting. B. MEFs expressing K13-ER TAM were treated with 4OHT and phosphorylation status of IKK1, IKK2 and IκBα was determined using <t>Pathscan</t> phospho-IKK1 <t>(Ser176/180),</t> phospho-IKK2 (Ser177/181), phosphor-IκBα (Ser32) ELISA kits, respectively.
Pathscan Phospho Ikkα, supplied by Cell Signaling Technology Inc, 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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Average 93 stars, based on 1 article reviews
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90
MyBiosource Biotechnology vegf-a (mbs024541)
A. Co-immunoprecipitation assay showing NEMO is essential for mediating the interaction of K13 with IKK1 and IKK2. FLAG-tagged K13 was immunoprecipitated from WT and NEMO-deficient Jurkat cells using control (C) and FLAG (F) antibody beads and presence of co-immunoprecipitated IKK1, IKK2 and NEMO detected by immunoblotting. B. MEFs expressing K13-ER TAM were treated with 4OHT and phosphorylation status of IKK1, IKK2 and IκBα was determined using <t>Pathscan</t> phospho-IKK1 <t>(Ser176/180),</t> phospho-IKK2 (Ser177/181), phosphor-IκBα (Ser32) ELISA kits, respectively.
Vegf A (Mbs024541), supplied by MyBiosource 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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Merck KGaA human insulin elisa kit
A. Co-immunoprecipitation assay showing NEMO is essential for mediating the interaction of K13 with IKK1 and IKK2. FLAG-tagged K13 was immunoprecipitated from WT and NEMO-deficient Jurkat cells using control (C) and FLAG (F) antibody beads and presence of co-immunoprecipitated IKK1, IKK2 and NEMO detected by immunoblotting. B. MEFs expressing K13-ER TAM were treated with 4OHT and phosphorylation status of IKK1, IKK2 and IκBα was determined using <t>Pathscan</t> phospho-IKK1 <t>(Ser176/180),</t> phospho-IKK2 (Ser177/181), phosphor-IκBα (Ser32) ELISA kits, respectively.
Human Insulin Elisa 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
https://www.bioz.com/product/180+elisa+kits/human+insulin+elisa+kit/pm36297065-86-15-19
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R&D Systems human epo quantikine ivd elisa 180 kit
A. Co-immunoprecipitation assay showing NEMO is essential for mediating the interaction of K13 with IKK1 and IKK2. FLAG-tagged K13 was immunoprecipitated from WT and NEMO-deficient Jurkat cells using control (C) and FLAG (F) antibody beads and presence of co-immunoprecipitated IKK1, IKK2 and NEMO detected by immunoblotting. B. MEFs expressing K13-ER TAM were treated with 4OHT and phosphorylation status of IKK1, IKK2 and IκBα was determined using <t>Pathscan</t> phospho-IKK1 <t>(Ser176/180),</t> phospho-IKK2 (Ser177/181), phosphor-IκBα (Ser32) ELISA kits, respectively.
Human Epo Quantikine Ivd Elisa 180 Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 95 stars, based on 1 article reviews
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90
MBL Life science mbl elisa kit
A. Co-immunoprecipitation assay showing NEMO is essential for mediating the interaction of K13 with IKK1 and IKK2. FLAG-tagged K13 was immunoprecipitated from WT and NEMO-deficient Jurkat cells using control (C) and FLAG (F) antibody beads and presence of co-immunoprecipitated IKK1, IKK2 and NEMO detected by immunoblotting. B. MEFs expressing K13-ER TAM were treated with 4OHT and phosphorylation status of IKK1, IKK2 and IκBα was determined using <t>Pathscan</t> phospho-IKK1 <t>(Ser176/180),</t> phospho-IKK2 (Ser177/181), phosphor-IκBα (Ser32) ELISA kits, respectively.
Mbl Elisa Kit, supplied by MBL Life science, 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/180+elisa+kits/elisa+kit+mbl/pmc09374178-19-21-42
Average 90 stars, based on 1 article reviews
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Endocrine Technologies elisa kit erk e3009
A. Co-immunoprecipitation assay showing NEMO is essential for mediating the interaction of K13 with IKK1 and IKK2. FLAG-tagged K13 was immunoprecipitated from WT and NEMO-deficient Jurkat cells using control (C) and FLAG (F) antibody beads and presence of co-immunoprecipitated IKK1, IKK2 and NEMO detected by immunoblotting. B. MEFs expressing K13-ER TAM were treated with 4OHT and phosphorylation status of IKK1, IKK2 and IκBα was determined using <t>Pathscan</t> phospho-IKK1 <t>(Ser176/180),</t> phospho-IKK2 (Ser177/181), phosphor-IκBα (Ser32) ELISA kits, respectively.
Elisa Kit Erk E3009, supplied by Endocrine Technologies, 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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Dia Pro Diagnostic Bioprobes Srl igg elisa kit dia.pro
Comparison of human CMV seroprevalence in different countries in Africa
Igg Elisa Kit Dia.Pro, supplied by Dia Pro Diagnostic Bioprobes Srl, 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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Dialab GmbH cmv igg elisa kit
Comparison of human <t> CMV </t> seroprevalence in different countries in Africa
Cmv Igg Elisa Kit, supplied by Dialab GmbH, 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/180+elisa+kits/enzyme+linked+immunosorbent+assay+3rd+generation+elisa+kits/pmc04967964-33-10-14
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96
Cell Signaling Technology Inc phospho p38
Effects of Pis-V10K and Pis-F2K/V10K on TLR2, TLR4, phospho-ERKs, phosphor-JNK, and <t>phosphor-p38</t> MAPK. TLR2, TLR4, phospho-ERKs, phosphor-JNK, and phosphor-p38 MAPK protein levels were determined by western blot analysis using specific antibodies.
Phospho P38, supplied by Cell Signaling Technology Inc, 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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Average 96 stars, based on 1 article reviews
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Becton Dickinson elisa kits
Effects of Pis-V10K and Pis-F2K/V10K on TLR2, TLR4, phospho-ERKs, phosphor-JNK, and <t>phosphor-p38</t> MAPK. TLR2, TLR4, phospho-ERKs, phosphor-JNK, and phosphor-p38 MAPK protein levels were determined by western blot analysis using specific antibodies.
Elisa Kits, supplied by Becton Dickinson, 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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R&D Systems human phospho p38 t180 y182 duoset ic elisa kit
Fig. 4. Effect of halofuginone on <t>p38</t> MAPK phosphoryla- tion. Halofuginone inhibits p38 MAPK phosphorylation in anti-CD3-activated T cells. The inhibition is dose-dependent. The data are means ( SD) of one representative experiment out of two performed.
Human Phospho P38 T180 Y182 Duoset Ic Elisa Kit, supplied by R&D Systems, 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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Image Search Results


HMJ-30 inhibits the Ras/MAPK, PI3K/AKT, and NF-κB signaling pathways in human osteogenic sarcoma U-2 OS cells. (A) Protein levels of Ras, p-ERK, p-JNK and p-p38 were downregulated, as determined by western blotting. Expression of the key proteins in MAPK signaling, (B) p-ERK (p-p44/42) and (C) p-p38, were reconfirmed using ELISA assays. (D) The protein levels of PI3K (p85) and p-AKT were downregulated, as determined by western blot-ting. (E) The key protein in p-AKT was reconfirmed by ELISA assay. (F) Protein levels of IKK, p-IκB and NF-κB (p65) were downregulated, as determined by western blotting. (G) NF-κB binding activity was determined using an electrophoretic mobility shift assay. Inhibitors of p44/22 MAPK (U0126), p38 (SB203580), PI3K (wortmannin) and NF-κB (PDTC), as positive controls, reduced protein kinase levels. The data represents the mean ± standard deviation of three experiments. *** P<0.001 vs. control. HMJ-30, 6-fluoro-2-(3-fluorophenyl)-4-(cyanoanilino)quinazoline; MAPK, mitogen-activated protein kinase; PI3K, phosphoinositide 3-kinase; AKT, protein kinase B; NF-κB, nuclear factor-κB; p-, phosphorylated; ERK, extracelullar signal-regulated kinase; JNK, c-Jun amino-terminal kinase; PDTC, ammonium pyrrolidinedithiocarbamate.

Journal: International Journal of Oncology

Article Title: Disruption of IGF-1R signaling by a novel quinazoline derivative, HMJ-30, inhibits invasiveness and reverses epithelial-mesenchymal transition in osteosarcoma U-2 OS cells

doi: 10.3892/ijo.2018.4325

Figure Lengend Snippet: HMJ-30 inhibits the Ras/MAPK, PI3K/AKT, and NF-κB signaling pathways in human osteogenic sarcoma U-2 OS cells. (A) Protein levels of Ras, p-ERK, p-JNK and p-p38 were downregulated, as determined by western blotting. Expression of the key proteins in MAPK signaling, (B) p-ERK (p-p44/42) and (C) p-p38, were reconfirmed using ELISA assays. (D) The protein levels of PI3K (p85) and p-AKT were downregulated, as determined by western blot-ting. (E) The key protein in p-AKT was reconfirmed by ELISA assay. (F) Protein levels of IKK, p-IκB and NF-κB (p65) were downregulated, as determined by western blotting. (G) NF-κB binding activity was determined using an electrophoretic mobility shift assay. Inhibitors of p44/22 MAPK (U0126), p38 (SB203580), PI3K (wortmannin) and NF-κB (PDTC), as positive controls, reduced protein kinase levels. The data represents the mean ± standard deviation of three experiments. *** P<0.001 vs. control. HMJ-30, 6-fluoro-2-(3-fluorophenyl)-4-(cyanoanilino)quinazoline; MAPK, mitogen-activated protein kinase; PI3K, phosphoinositide 3-kinase; AKT, protein kinase B; NF-κB, nuclear factor-κB; p-, phosphorylated; ERK, extracelullar signal-regulated kinase; JNK, c-Jun amino-terminal kinase; PDTC, ammonium pyrrolidinedithiocarbamate.

Article Snippet: p-IGF-1R β (Tyr1131) (cat. no. 7302), p-p38 MAPK (Thr180/Tyr182) (cat. no. 7946), p-p44/42 MAPK (Thr202/Tyr204) (cat. no. 7177), and p-Akt (Thr308) (cat. no. 7252) assays were performed according to the manufacturer's protocols (PathScan Sandwich ELISA kits; Cell Signaling Technology, Inc.).

Techniques: Protein-Protein interactions, Western Blot, Expressing, Enzyme-linked Immunosorbent Assay, Binding Assay, Activity Assay, Electrophoretic Mobility Shift Assay, Standard Deviation, Control

A. Co-immunoprecipitation assay showing NEMO is essential for mediating the interaction of K13 with IKK1 and IKK2. FLAG-tagged K13 was immunoprecipitated from WT and NEMO-deficient Jurkat cells using control (C) and FLAG (F) antibody beads and presence of co-immunoprecipitated IKK1, IKK2 and NEMO detected by immunoblotting. B. MEFs expressing K13-ER TAM were treated with 4OHT and phosphorylation status of IKK1, IKK2 and IκBα was determined using Pathscan phospho-IKK1 (Ser176/180), phospho-IKK2 (Ser177/181), phosphor-IκBα (Ser32) ELISA kits, respectively.

Journal: PLoS ONE

Article Title: Kaposi’s Sarcoma Associated Herpesvirus Encoded Viral FLICE Inhibitory Protein K13 Activates NF-κB Pathway Independent of TRAF6, TAK1 and LUBAC

doi: 10.1371/journal.pone.0036601

Figure Lengend Snippet: A. Co-immunoprecipitation assay showing NEMO is essential for mediating the interaction of K13 with IKK1 and IKK2. FLAG-tagged K13 was immunoprecipitated from WT and NEMO-deficient Jurkat cells using control (C) and FLAG (F) antibody beads and presence of co-immunoprecipitated IKK1, IKK2 and NEMO detected by immunoblotting. B. MEFs expressing K13-ER TAM were treated with 4OHT and phosphorylation status of IKK1, IKK2 and IκBα was determined using Pathscan phospho-IKK1 (Ser176/180), phospho-IKK2 (Ser177/181), phosphor-IκBα (Ser32) ELISA kits, respectively.

Article Snippet: The PathScan Phospho-IKKα (Ser176/180), Phospho-IKKβ (Ser177/181) sandwich ELISA Kits and PathScan Phospho-IκBα (Ser32) sandwich ELISA antibody pair (Cell Signaling, Danvers, MA) were used to detect endogenous levels of IKKα, IKKβ and IκBα proteins when phosphorylated at Ser176/180, Ser177/181 and Ser32, respectively.

Techniques: Co-Immunoprecipitation Assay, Immunoprecipitation, Control, Western Blot, Expressing, Phospho-proteomics, Enzyme-linked Immunosorbent Assay

Comparison of human CMV seroprevalence in different countries in Africa

Journal: Journal of Virus Eradication

Article Title: Human cytomegalovirus (CMV) in Africa: a neglected but important pathogen

doi:

Figure Lengend Snippet: Comparison of human CMV seroprevalence in different countries in Africa

Article Snippet: Nigeria (Ilorin) , 93.9% , Asymptomatic HIV-positive adults , 180 , IgG ELISA Kit (DIA.PRO, Diagnostic Bioprobes, Italy) , .

Techniques: Comparison, Enzyme-linked Immunosorbent Assay, Agglutination, Cell Counting, Diagnostic Assay, Virus, Immunofluorescence

Comparison of human  CMV  seroprevalence in different countries in Africa

Journal: Journal of Virus Eradication

Article Title: Human cytomegalovirus (CMV) in Africa: a neglected but important pathogen

doi:

Figure Lengend Snippet: Comparison of human CMV seroprevalence in different countries in Africa

Article Snippet: Nigeria (Kano) , 91.1% , Pregnant women , 180 , CMV IgG ELISA kit (Dialab, Austria) , .

Techniques: Comparison, Enzyme-linked Immunosorbent Assay, Agglutination, Cell Counting, Diagnostic Assay, Virus, Immunofluorescence

Effects of Pis-V10K and Pis-F2K/V10K on TLR2, TLR4, phospho-ERKs, phosphor-JNK, and phosphor-p38 MAPK. TLR2, TLR4, phospho-ERKs, phosphor-JNK, and phosphor-p38 MAPK protein levels were determined by western blot analysis using specific antibodies.

Journal: PLoS ONE

Article Title: Role of Phenylalanine and Valine 10 Residues in the Antimicrobial Activity and Cytotoxicity of Piscidin-1

doi: 10.1371/journal.pone.0114453

Figure Lengend Snippet: Effects of Pis-V10K and Pis-F2K/V10K on TLR2, TLR4, phospho-ERKs, phosphor-JNK, and phosphor-p38 MAPK. TLR2, TLR4, phospho-ERKs, phosphor-JNK, and phosphor-p38 MAPK protein levels were determined by western blot analysis using specific antibodies.

Article Snippet: The membrane was blocked by incubating with 5% bovine serum albumin (BSA) in TBST (25 mM Tris, 3 mM KCl, 140 mM NaCl, 0.1% Tween 20) for 1 h at RT, and then incubated with antibodies specific for toll-like receptor 2 (TLR2, 1∶2000; Cell Signaling Technology, Beverly, MA, USA), TLR4 (1∶2000; Cell Signaling Technology), phospho-p38 (1∶2000; Cell signaling Technology), phospho-ERK (1∶2000; Cell signaling Technology), phospho-JNK (1∶2000; Cell signaling Technology), and β-actin (1∶5000, Sigma-Aldrich, St. Louis, MO, USA).

Techniques: Western Blot

Fig. 4. Effect of halofuginone on p38 MAPK phosphoryla- tion. Halofuginone inhibits p38 MAPK phosphorylation in anti-CD3-activated T cells. The inhibition is dose-dependent. The data are means ( SD) of one representative experiment out of two performed.

Journal: Journal of leukocyte biology

Article Title: Halofuginone inhibits NF-kappaB and p38 MAPK in activated T cells.

doi: 10.1189/jlb.0705409

Figure Lengend Snippet: Fig. 4. Effect of halofuginone on p38 MAPK phosphoryla- tion. Halofuginone inhibits p38 MAPK phosphorylation in anti-CD3-activated T cells. The inhibition is dose-dependent. The data are means ( SD) of one representative experiment out of two performed.

Article Snippet: Phosphorylation of p38 was determined using the Human Phospho-p38 (T180/Y182) DuoSet IC ELISA kit (R&D Systems), according to the manufacturer’s instructions.

Techniques: Phospho-proteomics, Inhibition