pstat2 Search Results


pstat2  (Carl Zeiss)
90
Carl Zeiss pstat2
Absence of pSTAT1 and <t>pSTAT2</t> nuclear translocation in IFN-α treated rat neurons. a–d Primary dissociated neuronal cultures of rat hippocampi were treated with IFN-α (105 U/ml) for the indicated time points and for the presence of phosphorylated STAT1 (α-pSTAT1) or STAT2 (α-pSTAT1) in astrocytes (α-GFAP) or neurons (α-Map-2) Scale bars 10 μm. Lower panels indicate the fluorescence intensity along the dashed line shown in the middle panels. e, f Statistical analysis of the mean fluorescence intensity (MFI) of pSTAT1 and pSTAT2 in astrocytes (n = 30) and neurons (n = 30) treated with IFN-α (105 U/ml) for the indicated time points. g IFN-α receptor 1 (IFNAR1) surface staining (α-IFNAR1) of neurons (α-Map-2). IFNAR1 staining was carried out with non-permeabilized neurons. For subsequent staining with Map-2, cell were extensively washed, treated with detergent and subsequently stained with anti-Map-2 antibodies. Ctrl w/o 1st AB, staining of non-permeabilized neurons with secondary antibodies only. Scale bars 10 μm
Pstat2, supplied by Carl Zeiss, 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/pstat2/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
pstat2 - by Bioz Stars, 2026-02
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pab directed against phospho- stat2 (tyr689) antibody  (Merck KGaA)
90
Merck KGaA pab directed against phospho- stat2 (tyr689) antibody
Absence of pSTAT1 and <t>pSTAT2</t> nuclear translocation in IFN-α treated rat neurons. a–d Primary dissociated neuronal cultures of rat hippocampi were treated with IFN-α (105 U/ml) for the indicated time points and for the presence of phosphorylated STAT1 (α-pSTAT1) or STAT2 (α-pSTAT1) in astrocytes (α-GFAP) or neurons (α-Map-2) Scale bars 10 μm. Lower panels indicate the fluorescence intensity along the dashed line shown in the middle panels. e, f Statistical analysis of the mean fluorescence intensity (MFI) of pSTAT1 and pSTAT2 in astrocytes (n = 30) and neurons (n = 30) treated with IFN-α (105 U/ml) for the indicated time points. g IFN-α receptor 1 (IFNAR1) surface staining (α-IFNAR1) of neurons (α-Map-2). IFNAR1 staining was carried out with non-permeabilized neurons. For subsequent staining with Map-2, cell were extensively washed, treated with detergent and subsequently stained with anti-Map-2 antibodies. Ctrl w/o 1st AB, staining of non-permeabilized neurons with secondary antibodies only. Scale bars 10 μm
Pab Directed Against Phospho Stat2 (Tyr689) Antibody, 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/result/pab directed against phospho- stat2 (tyr689) antibody/product/Merck KGaA
Average 90 stars, based on 1 article reviews
pab directed against phospho- stat2 (tyr689) antibody - by Bioz Stars, 2026-02
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primary cell pstat2 assay  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc primary cell pstat2 assay
Absence of pSTAT1 and <t>pSTAT2</t> nuclear translocation in IFN-α treated rat neurons. a–d Primary dissociated neuronal cultures of rat hippocampi were treated with IFN-α (105 U/ml) for the indicated time points and for the presence of phosphorylated STAT1 (α-pSTAT1) or STAT2 (α-pSTAT1) in astrocytes (α-GFAP) or neurons (α-Map-2) Scale bars 10 μm. Lower panels indicate the fluorescence intensity along the dashed line shown in the middle panels. e, f Statistical analysis of the mean fluorescence intensity (MFI) of pSTAT1 and pSTAT2 in astrocytes (n = 30) and neurons (n = 30) treated with IFN-α (105 U/ml) for the indicated time points. g IFN-α receptor 1 (IFNAR1) surface staining (α-IFNAR1) of neurons (α-Map-2). IFNAR1 staining was carried out with non-permeabilized neurons. For subsequent staining with Map-2, cell were extensively washed, treated with detergent and subsequently stained with anti-Map-2 antibodies. Ctrl w/o 1st AB, staining of non-permeabilized neurons with secondary antibodies only. Scale bars 10 μm
Primary Cell Pstat2 Assay, supplied by STEMCELL Technologies 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/result/primary cell pstat2 assay/product/STEMCELL Technologies Inc
Average 90 stars, based on 1 article reviews
primary cell pstat2 assay - by Bioz Stars, 2026-02
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anti-pstat2 at tyr-690  (ImmunoWay Biotechnology Company)
90
ImmunoWay Biotechnology Company anti-pstat2 at tyr-690
Absence of pSTAT1 and <t>pSTAT2</t> nuclear translocation in IFN-α treated rat neurons. a–d Primary dissociated neuronal cultures of rat hippocampi were treated with IFN-α (105 U/ml) for the indicated time points and for the presence of phosphorylated STAT1 (α-pSTAT1) or STAT2 (α-pSTAT1) in astrocytes (α-GFAP) or neurons (α-Map-2) Scale bars 10 μm. Lower panels indicate the fluorescence intensity along the dashed line shown in the middle panels. e, f Statistical analysis of the mean fluorescence intensity (MFI) of pSTAT1 and pSTAT2 in astrocytes (n = 30) and neurons (n = 30) treated with IFN-α (105 U/ml) for the indicated time points. g IFN-α receptor 1 (IFNAR1) surface staining (α-IFNAR1) of neurons (α-Map-2). IFNAR1 staining was carried out with non-permeabilized neurons. For subsequent staining with Map-2, cell were extensively washed, treated with detergent and subsequently stained with anti-Map-2 antibodies. Ctrl w/o 1st AB, staining of non-permeabilized neurons with secondary antibodies only. Scale bars 10 μm
Anti Pstat2 At Tyr 690, supplied by ImmunoWay Biotechnology Company, 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-pstat2 at tyr-690/product/ImmunoWay Biotechnology Company
Average 90 stars, based on 1 article reviews
anti-pstat2 at tyr-690 - by Bioz Stars, 2026-02
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rabbit polyclonal anti-pstat2 igg  (Upstate Biotechnology Inc)
90
Upstate Biotechnology Inc rabbit polyclonal anti-pstat2 igg
Absence of pSTAT1 and <t>pSTAT2</t> nuclear translocation in IFN-α treated rat neurons. a–d Primary dissociated neuronal cultures of rat hippocampi were treated with IFN-α (105 U/ml) for the indicated time points and for the presence of phosphorylated STAT1 (α-pSTAT1) or STAT2 (α-pSTAT1) in astrocytes (α-GFAP) or neurons (α-Map-2) Scale bars 10 μm. Lower panels indicate the fluorescence intensity along the dashed line shown in the middle panels. e, f Statistical analysis of the mean fluorescence intensity (MFI) of pSTAT1 and pSTAT2 in astrocytes (n = 30) and neurons (n = 30) treated with IFN-α (105 U/ml) for the indicated time points. g IFN-α receptor 1 (IFNAR1) surface staining (α-IFNAR1) of neurons (α-Map-2). IFNAR1 staining was carried out with non-permeabilized neurons. For subsequent staining with Map-2, cell were extensively washed, treated with detergent and subsequently stained with anti-Map-2 antibodies. Ctrl w/o 1st AB, staining of non-permeabilized neurons with secondary antibodies only. Scale bars 10 μm
Rabbit Polyclonal Anti Pstat2 Igg, supplied by Upstate Biotechnology 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/result/rabbit polyclonal anti-pstat2 igg/product/Upstate Biotechnology Inc
Average 90 stars, based on 1 article reviews
rabbit polyclonal anti-pstat2 igg - by Bioz Stars, 2026-02
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antibodies for pstat2  (Carl Roth GmbH)
90
Carl Roth GmbH antibodies for pstat2
Absence of pSTAT1 and <t>pSTAT2</t> nuclear translocation in IFN-α treated rat neurons. a–d Primary dissociated neuronal cultures of rat hippocampi were treated with IFN-α (105 U/ml) for the indicated time points and for the presence of phosphorylated STAT1 (α-pSTAT1) or STAT2 (α-pSTAT1) in astrocytes (α-GFAP) or neurons (α-Map-2) Scale bars 10 μm. Lower panels indicate the fluorescence intensity along the dashed line shown in the middle panels. e, f Statistical analysis of the mean fluorescence intensity (MFI) of pSTAT1 and pSTAT2 in astrocytes (n = 30) and neurons (n = 30) treated with IFN-α (105 U/ml) for the indicated time points. g IFN-α receptor 1 (IFNAR1) surface staining (α-IFNAR1) of neurons (α-Map-2). IFNAR1 staining was carried out with non-permeabilized neurons. For subsequent staining with Map-2, cell were extensively washed, treated with detergent and subsequently stained with anti-Map-2 antibodies. Ctrl w/o 1st AB, staining of non-permeabilized neurons with secondary antibodies only. Scale bars 10 μm
Antibodies For Pstat2, supplied by Carl Roth 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/result/antibodies for pstat2/product/Carl Roth GmbH
Average 90 stars, based on 1 article reviews
antibodies for pstat2 - by Bioz Stars, 2026-02
90/100 stars
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Image Search Results


Absence of pSTAT1 and pSTAT2 nuclear translocation in IFN-α treated rat neurons. a–d Primary dissociated neuronal cultures of rat hippocampi were treated with IFN-α (105 U/ml) for the indicated time points and for the presence of phosphorylated STAT1 (α-pSTAT1) or STAT2 (α-pSTAT1) in astrocytes (α-GFAP) or neurons (α-Map-2) Scale bars 10 μm. Lower panels indicate the fluorescence intensity along the dashed line shown in the middle panels. e, f Statistical analysis of the mean fluorescence intensity (MFI) of pSTAT1 and pSTAT2 in astrocytes (n = 30) and neurons (n = 30) treated with IFN-α (105 U/ml) for the indicated time points. g IFN-α receptor 1 (IFNAR1) surface staining (α-IFNAR1) of neurons (α-Map-2). IFNAR1 staining was carried out with non-permeabilized neurons. For subsequent staining with Map-2, cell were extensively washed, treated with detergent and subsequently stained with anti-Map-2 antibodies. Ctrl w/o 1st AB, staining of non-permeabilized neurons with secondary antibodies only. Scale bars 10 μm

Journal: Cellular and Molecular Life Sciences: CMLS

Article Title: Absence of a robust innate immune response in rat neurons facilitates persistent infection of Borna disease virus in neuronal tissue

doi: 10.1007/s00018-013-1402-5

Figure Lengend Snippet: Absence of pSTAT1 and pSTAT2 nuclear translocation in IFN-α treated rat neurons. a–d Primary dissociated neuronal cultures of rat hippocampi were treated with IFN-α (105 U/ml) for the indicated time points and for the presence of phosphorylated STAT1 (α-pSTAT1) or STAT2 (α-pSTAT1) in astrocytes (α-GFAP) or neurons (α-Map-2) Scale bars 10 μm. Lower panels indicate the fluorescence intensity along the dashed line shown in the middle panels. e, f Statistical analysis of the mean fluorescence intensity (MFI) of pSTAT1 and pSTAT2 in astrocytes (n = 30) and neurons (n = 30) treated with IFN-α (105 U/ml) for the indicated time points. g IFN-α receptor 1 (IFNAR1) surface staining (α-IFNAR1) of neurons (α-Map-2). IFNAR1 staining was carried out with non-permeabilized neurons. For subsequent staining with Map-2, cell were extensively washed, treated with detergent and subsequently stained with anti-Map-2 antibodies. Ctrl w/o 1st AB, staining of non-permeabilized neurons with secondary antibodies only. Scale bars 10 μm

Article Snippet: Phospho-STAT quantification Immunofluorescence images from neurons and astrocytes stained against pSTAT1 or pSTAT2 were obtained by Zeiss, Germany ApoTome and processed under the same software (AxioVision, Zeiss, Germany) settings.

Techniques: Translocation Assay, Fluorescence, Staining