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anti pstat1 tyr 701  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti pstat1 tyr 701
    Anti Pstat1 Tyr 701, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+pstat1+tyr+701/10__1042_slash_bcj20253246-373-20-27
    Average 86 stars, based on 1 article reviews
    anti pstat1 tyr 701 - by Bioz Stars, 2026-10
    86/100 stars

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    other:

    Article Title: Artemether and Euphorbia Factor L9 suppress kynurenine production through distinct effects on Tryptophan metabolism.
    Article Snippet: The m ost up-to-date-version is available at https://doi.org/10.1042/BC J20253246 Capatina et al. 24 4 °C (1:1000): anti-PD-L1 (E1L3N), anti-STAT1 (9172), anti-pSTAT1 Tyr-701 (D4A7), antiIDO1 (D5J4E) all from Cell Signaling Technology, while anti-IDO2 (30530-1-AP) and antiTDO2 (15880-1-AP) antibodies were purchased from Proteintech.

    Article Title: Biallelic JAK1 mutations in immunodeficient patient with mycobacterial infection
    Article Snippet: The following Abs were used: anti-JAK1 (610231, BD Biosciences; 1/1,000 dilution), anti-pJAK1 Tyr 1022/1023 (3331, Cell Signaling Technology; 1/1,000 dilution), anti-JAK2 (Clone D2E12, 3230, Cell Signaling Technology; 1/1,000), anti-pJAK2 Tyr 1007/1008 (Clone C80C, 33776, Cell Signaling Technology; 1:1,000), anti-TYK2 (Clone D4I5T, 14193, Cell Signaling Technology; 1:1,000), anti-pTYK2 Tyr 1054/1055 (Clone C80C, 9321, Cell Signaling Technology; 1:1,000), anti-STAT1 (9172, Cell Signaling Technology; 1:1,000), anti-pSTAT1 Tyr 701 (Clone 58D6, 9167, Cell Signaling Technology; 1:1,000), anti-STAT2 (4594, Cell Signaling Technology; 1:1,000), anti-pSTAT2 Tyr 689 (07–224, Millipore; 1:2,000), anti-β-Actin (Clone AC-15, A5451, Sigma-Aldrich; 1:10,000), anti-GFP (11814460001, Roche or ab290, AbCam; 1:2,000) and anti-Myc (clone 9B11, 2276, Cell Signaling Technology; 1:1,000).

    Article Title: Artemether and Euphorbia Factor L9 suppress kynurenine production through distinct effects on Tryptophan metabolism
    Article Snippet: The following antibodies were probed overnight at 4 °C (1:1000): anti-PD-L1 (E1L3N), anti-STAT1 (9172), anti-pSTAT1 Tyr-701 (D4A7), anti-IDO1 (D5J4E) all from Cell Signaling Technology.

    Article Title: Met inhibition revokes IFNγ-induction of PD-1 ligands in MET-amplified tumours
    Article Snippet: Protein detection was performed by using the following primary antibodies, diluted as indicated: anti-human MET (3D4, 1:3000, Invitrogen Corp., Camarillo, CA), anti-pMET Tyr 1234/1235 (D26, 1:1000), anti-JAK1 (6G4, 1:1000), anti-pJAK1 Tyr 1022/1023 (1:1000), anti-JAK2 (D2E12, 1:1000), anti-pJAK2 Tyr 1007/1008 (1:1000) anti-STAT1 (1:1000), anti-pSTAT1 Tyr 701 (58D6, 1:1000), anti-PD-L1 (E1L3N, 1:1000), anti-GAPDH (D4C6R, 1:1000) (all from Cell Signaling Technology, Beverly, MA), anti-IFNGR1 (EPR7866, 1:1000, Abcam, Cambridge, UK) and anti-Vinculin (hVIN-1, 1:1000, Sigma Life Sciences).



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    Phosphorylation of STAT1 <t>(pSTAT1)</t> after stimulation with IFNα was assessed by flow cytometry in STAT1-GOF patients (black color) and healthy controls (gray color). In STAT1-GOF patients the expected increase of pSTAT1 was statistically significant compared to healthy controls and was significantly reversed by the JAK inhibitor ruxolitinib with a dose-dependent effect. US , unstimulated
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    Phosphorylation of STAT1 <t>(pSTAT1)</t> after stimulation with IFNα was assessed by flow cytometry in STAT1-GOF patients (black color) and healthy controls (gray color). In STAT1-GOF patients the expected increase of pSTAT1 was statistically significant compared to healthy controls and was significantly reversed by the JAK inhibitor ruxolitinib with a dose-dependent effect. US , unstimulated
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    Phosphorylation of STAT1 (pSTAT1) after stimulation with IFNα was assessed by flow cytometry in STAT1-GOF patients (black color) and healthy controls (gray color). In STAT1-GOF patients the expected increase of pSTAT1 was statistically significant compared to healthy controls and was significantly reversed by the JAK inhibitor ruxolitinib with a dose-dependent effect. US , unstimulated

    Journal: Journal of Clinical Immunology

    Article Title: Patients with STAT1 Gain-of-function Mutations Display Increased Apoptosis which is Reversed by the JAK Inhibitor Ruxolitinib

    doi: 10.1007/s10875-024-01684-y

    Figure Lengend Snippet: Phosphorylation of STAT1 (pSTAT1) after stimulation with IFNα was assessed by flow cytometry in STAT1-GOF patients (black color) and healthy controls (gray color). In STAT1-GOF patients the expected increase of pSTAT1 was statistically significant compared to healthy controls and was significantly reversed by the JAK inhibitor ruxolitinib with a dose-dependent effect. US , unstimulated

    Article Snippet: Intracellular staining of activated STAT1 protein was performed with phycoerythrin (PE)-conjugated mouse anti-pSTAT1-Tyr-701 IgG mAb (BD Pharmigene) and isotype-matched mAb PE (BD Bioscence).

    Techniques: Flow Cytometry

    ATP1A1 knockdown enhances cardiac glycoside-mediated inhibition of STAT1(Y701) phosphorylation. A , representative levels of pSTAT1(Y701) and total STAT1 are shown for the MDA-MB-231 ouabain and digoxin experiments in <xref ref-type=Figure 4 . For loading controls, see Figure 4 , D and E . B , representative levels of pSTAT1(Y701) and total STAT1 are shown for the A549 ouabain and digoxin experiments in Figure 5 . For loading controls, see Figure 5 , C and D . The dashed vertical lines indicate one lane (ladder) that has been spliced out. C , quantification of pSTAT1(Y701) in western blots of NTC or ATP1A1 siRNA transfected TNF/IFN-ɣ (24 h) stimulated MDA-MB-231 cells treated with 100 nM ouabain. ∗ p < 0.05, ∗∗∗ p < 0.001, Two-factor ANOVA, Tukey’s multiple comparisons. D , STAT1 activation time-course experiment in MDA-MB-231 cells treated with 100 nM ouabain or 0.05% DMSO and stimulated for 30 min, 2 h, 8 h, or 24 h with TNF/IFN-γ. Mean intensities ±standard deviation, measured by densitometry of blots from three independent time-course experiments, are listed under the pSTAT1(Y701) long and total STAT1 panels. " width="100%" height="100%">

    Journal: The Journal of Biological Chemistry

    Article Title: Inhibition of the Na + /K + -ATPase by cardiac glycosides suppresses expression of the IDO1 immune checkpoint in cancer cells by reducing STAT1 activation

    doi: 10.1016/j.jbc.2022.101707

    Figure Lengend Snippet: ATP1A1 knockdown enhances cardiac glycoside-mediated inhibition of STAT1(Y701) phosphorylation. A , representative levels of pSTAT1(Y701) and total STAT1 are shown for the MDA-MB-231 ouabain and digoxin experiments in Figure 4 . For loading controls, see Figure 4 , D and E . B , representative levels of pSTAT1(Y701) and total STAT1 are shown for the A549 ouabain and digoxin experiments in Figure 5 . For loading controls, see Figure 5 , C and D . The dashed vertical lines indicate one lane (ladder) that has been spliced out. C , quantification of pSTAT1(Y701) in western blots of NTC or ATP1A1 siRNA transfected TNF/IFN-ɣ (24 h) stimulated MDA-MB-231 cells treated with 100 nM ouabain. ∗ p < 0.05, ∗∗∗ p < 0.001, Two-factor ANOVA, Tukey’s multiple comparisons. D , STAT1 activation time-course experiment in MDA-MB-231 cells treated with 100 nM ouabain or 0.05% DMSO and stimulated for 30 min, 2 h, 8 h, or 24 h with TNF/IFN-γ. Mean intensities ±standard deviation, measured by densitometry of blots from three independent time-course experiments, are listed under the pSTAT1(Y701) long and total STAT1 panels.

    Article Snippet: Membranes were blocked with 2% BSA at least 1 h at room temperature and probed overnight at 4 °C (1:1000) for the following primary antibodies to PD-L1 (E1L3N), STAT1 (9172), pSTAT1 Tyr-701 (D4A7), SOCS3 (2923S), IDO1 (D5J4E) all from Cell Signaling Technology, or ATP1A1 (ab7671 464.6), from Abcam, and for 1 h at room temperature for GAPDH (6C5), from Abcam.

    Techniques: Knockdown, Inhibition, Phospho-proteomics, Western Blot, Transfection, Activation Assay, Standard Deviation