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Rabbit Anti STAT1 Polyclonal Affinity Purified (PBS with 0.02% sodium azide, 50% glycerol, pH7.3) (Immunofluorescence) from Innovative Research is a polyclonal antibody in a liquid format, buffered in PBS with 0.02% sodium azide, 50% glycerol,
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Cusabio
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Boster Bio
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Bio-Rad
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BIOKE Inc
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Bioworld Antibodies
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Autogen-Bioclear ltd
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EnoGene Inc
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Rabbit anti-Human STAT1 Polyclonal Antibody
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Image Search Results
Journal: Frontiers in Pharmacology
Article Title: Adiponectin Interacts In-Vitro With Cementoblasts Influencing Cell Migration, Proliferation and Cementogenesis Partly Through the MAPK Signaling Pathway
doi: 10.3389/fphar.2020.585346
Figure Lengend Snippet: Adiponectin promotes JNK, ERK1/2 and P38 phosphorylation on OCCM-30 cells. (A,B) The expression of JNK (46 and 54 kDa), ERK1/2 (42 and 44 kDa) and P38 (42 kDa) expression as well as their phosphorylated forms after Adiponectin (20 ng/ml) stimulation were analyzed by Western Blots. β-actin served as a loading control. Graphics show the relative expression of p-JNK, p-ERK1/2 and p-P38 compared to cells at time point 0 min. (C,D) Adiponectin (20 ng/ml) promotes STAT1 (98 KDa) and STAT3 (85 KDa) phosphorylation during a period of 30 min. Graphics show the relative expression of p-STAT1 and p-STAT3 compared to cells at time point 0 min. Values are expressed as means ± SD: Ns (not significant), * p < 0.05; ** p < 0.01; *** p < 0.001.
Article Snippet: The membranes were blocked with 5% non-fat milk (T145.1, ROTH) for 1 h and incubated with the primary antibodies for Adiponectin Receptor 1 (ab70362, Abcam); Adiponectin Receptor 2 (ab77612, Abcam); ERK1/2 (MBS8241746, BIOZOL); phospho-ERK1/2 (44-680G, Thermo-Fisher); P54/P46 JNK (#9252, Cell Signaling Technology), phospho-JNK (07-175, Thermo-Fisher); P38 MAPK (#9212, Cell Signaling Technology); phospho-P38 MAPK Alpha (#4511, Cell Signaling Technology),
Techniques: Phospho-proteomics, Expressing, Western Blot, Control
Journal: PLoS ONE
Article Title: Alpha-Synuclein Proteins Promote Pro-Inflammatory Cascades in Microglia: Stronger Effects of the A53T Mutant
doi: 10.1371/journal.pone.0162717
Figure Lengend Snippet: After 30 min, 1 h, 3 h or 6 h of A53T protein exposure (5 μM), microglial cell lysates were subjected to western-blot analysis (Fig 5A) to determine the expression of phospho-Stat1 (pStat1), phospho-p38 (pp38) and phospho-ERK (pERK). α-Tubulin (αTub) was used as a loading control. These chemiluminescent detection assays were realized with 20 μg of total proteins. Ratios between phosphorylated versus non-phosphorylated proteins, called pStat1/Stat1, pp38/p38 and pERK/ERK, were described in Fig 5B. Results are given as mean ± SEM of at least three independent experiments. * p < 0.05, significantly different from control condition.
Article Snippet: Blots were incubated with a mouse anti-Stat1 (1:500, BD Biosciences, Belgium),
Techniques: Western Blot, Expressing