rabbit anti stat1 Search Results


93
Bioss stat1(s727) (8a1) monoclonal antibody
Stat1(s727) (8a1) Monoclonal Antibody, supplied by Bioss, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+stat1/STAT1(S727)+(8A1)+Monoclonal+Antibody/custom%40bsm-52209r%4037800555
Average 93 stars, based on 1 article reviews
stat1(s727) (8a1) monoclonal antibody - by Bioz Stars, 2026-10
93/100 stars
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N/A
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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92
Cusabio technology
Technology, supplied by Cusabio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+stat1/Rabbit+anti-+STAT1+Polyclonal+Antibody/pmc11241421-54-7-6
Average 92 stars, based on 1 article reviews
technology - by Bioz Stars, 2026-10
92/100 stars
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91
Bio-Rad stat1
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 <t>STAT1</t> (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.
Stat1, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+stat1/Rabbit+anti+STAT1/pmc07783624-58-58-60
Average 91 stars, based on 1 article reviews
stat1 - by Bioz Stars, 2026-10
91/100 stars
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93
Boster Bio anti stat1 antibody rabbit
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 <t>STAT1</t> (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.
Anti Stat1 Antibody Rabbit, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+stat1/Anti-STAT1+Rabbit+Monoclonal+Antibody/pmc09029761-125-0-10
Average 93 stars, based on 1 article reviews
anti stat1 antibody rabbit - by Bioz Stars, 2026-10
93/100 stars
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85
Bio-Rad phospho stat1 tyr701 rabbit mab
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 <t>STAT1</t> (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.
Phospho Stat1 Tyr701 Rabbit Mab, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+anti+stat1/Rabbit+anti+STAT1+(pTyr701)/us10858395-405-10-8
Average 85 stars, based on 1 article reviews
phospho stat1 tyr701 rabbit mab - by Bioz Stars, 2026-10
85/100 stars
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90
BIOKE Inc rabbit anti-phospho-stat1
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 <t>phospho-Stat1</t> (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.
Rabbit Anti Phospho Stat1, supplied by BIOKE Inc, 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/rabbit+anti+stat1/rabbit+anti+phospho+stat1/pmc05021287-120-11-14
Average 90 stars, based on 1 article reviews
rabbit anti-phospho-stat1 - by Bioz Stars, 2026-10
90/100 stars
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90
Bioworld Antibodies rabbit anti-stat1 (1:500 dilution)
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 <t>phospho-Stat1</t> (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.
Rabbit Anti Stat1 (1:500 Dilution), 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/product/rabbit+anti+stat1/anti+antibody+rabbit+stat1/pm23588992-41-16-20
Average 90 stars, based on 1 article reviews
rabbit anti-stat1 (1:500 dilution) - by Bioz Stars, 2026-10
90/100 stars
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90
Autogen-Bioclear ltd rabbit anti-stat1 antibody
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 <t>phospho-Stat1</t> (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.
Rabbit Anti Stat1 Antibody, 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/product/rabbit+anti+stat1/rabbit+anti+stat1+antibody/10__1128_slash_jvi__02829___13-101-75-78
Average 90 stars, based on 1 article reviews
rabbit anti-stat1 antibody - by Bioz Stars, 2026-10
90/100 stars
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90
EnoGene Inc anti-stat1 (ab-701) rabbit polyclonal
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 <t>phospho-Stat1</t> (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.
Anti Stat1 (Ab 701) Rabbit Polyclonal, supplied by EnoGene Inc, 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/rabbit+anti+stat1/anti+stat1++ab+701++rabbit+polyclonal/pm26592235-190-18-22
Average 90 stars, based on 1 article reviews
anti-stat1 (ab-701) rabbit polyclonal - by Bioz Stars, 2026-10
90/100 stars
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Rabbit anti-Human STAT1 Polyclonal Antibody
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Image Search Results


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.

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), STAT1 (AHP2527, Bio-Rad); phospho-STAT1 Tyr701 (05-1064, Thermo-Fisher); phospho-STAT1 S727 (ab109461, Abcam); STAT3 (PA1-86605, Thermo-Fisher); phospho-STAT3 S727 (OPA1-03007, Thermo-Fisher), and β-actin (ab8227, Abcam) at a concentration of 1:1,000.

Techniques: Phospho-proteomics, Expressing, Western Blot, Control

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.

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), rabbit anti-phospho-Stat1 (1:1000, Bioke, The Netherlands), rabbit anti-p38 (1:1000, Calbiochem, Belgium), rabbit anti-phospho-p38 (1:1000, Bioke), rabbit anti-ERK (1:20000, Sigma), rabbit anti-phospho-ERK (1:2000, Bioke), mouse anti-α-tubulin (1:5000, AbCam, UK), rabbit anti-p65 (1:200, Santa Cruz Biotechnologies, Germany), rabbit anti-c-Fos (1:1000, Bioke), rabbit anti-Nrf2 (1:1000, Bioke) and mouse anti-HDAC1 (1:2000, AbCam) antibody.

Techniques: Western Blot, Expressing