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phospho stat5  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc phospho stat5
    Phospho Stat5, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 334 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phospho+stat5/Phospho-Stat5+(Tyr694)+XP+Rabbit+mAb/pmc13049607-338-59-61
    Average 96 stars, based on 334 article reviews
    phospho stat5 - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Saline:

    Article Title: Translation factor eIF4G2 directs CD8 + T cell lineage commitment by selectively enabling the IL-7 receptor response
    Article Snippet: Proteins were separated by SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto polyvinylidene difluoride (PVDF) membranes (Millipore). .. Membranes were blocked with 5% non-fat milk or bovine serum albumin (BSA) in Tris-buffered saline containing 0.1% Tween-20 (TBST) for 1 hour at room temperature and then incubated overnight at 4 °C with the following primary antibodies diluted in blocking buffer: eIF4G2 (CST, 3468S), β-actin (CST, 3700S), eIF4G1 (Proteintech, 15704-1-AP), IL-7Rα (Proteintech, 17626-1-AP), γc (Proteintech, 11409-1-AP), STAT5 (Proteintech, 13179-1-AP), phospho STAT5 (CST, 4322T), STAT6 (Proteintech, 51073-1-AP), mouse phospho STAT6 (CST, 56554S). .. After washing with TBST, membranes were incubated with horseradish peroxidase (HRP)-conjugated goat anti-mouse or anti-rabbit secondary antibody (Proteintech, SA00001-1; SA00001-9) for 1 hour at room temperature.

    Incubation:

    Article Title: Translation factor eIF4G2 directs CD8 + T cell lineage commitment by selectively enabling the IL-7 receptor response
    Article Snippet: Proteins were separated by SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto polyvinylidene difluoride (PVDF) membranes (Millipore). .. Membranes were blocked with 5% non-fat milk or bovine serum albumin (BSA) in Tris-buffered saline containing 0.1% Tween-20 (TBST) for 1 hour at room temperature and then incubated overnight at 4 °C with the following primary antibodies diluted in blocking buffer: eIF4G2 (CST, 3468S), β-actin (CST, 3700S), eIF4G1 (Proteintech, 15704-1-AP), IL-7Rα (Proteintech, 17626-1-AP), γc (Proteintech, 11409-1-AP), STAT5 (Proteintech, 13179-1-AP), phospho STAT5 (CST, 4322T), STAT6 (Proteintech, 51073-1-AP), mouse phospho STAT6 (CST, 56554S). .. After washing with TBST, membranes were incubated with horseradish peroxidase (HRP)-conjugated goat anti-mouse or anti-rabbit secondary antibody (Proteintech, SA00001-1; SA00001-9) for 1 hour at room temperature.

    Article Title: Inhibition of the JAK/STAT Signaling Pathway Suggests a Protective Effect against Acantholysis in Pemphigus
    Article Snippet: .. For specific protein identification, the membrane was blocked for 1 h at room temperature in LI-COR blocking buffer and incubated over night at 4 °C with primary antibodies recognizing actin (clone C4, 1:5000, Merck, Darmstadt, Germany or clone 13E5, 1:1000, Cell Signaling, Danvers, USA), phospho-STAT1 (Tyr701, clone 58D6, 1:1000), phospho-STAT3 (Tyr705, polyclonal, 1:1000), phospho-STAT4 (Tyr693, clone D2E4, 1:1000), phospho-STAT5 (Tyr694, clone C71E5, 1:1000), phospho-STAT6 (Tyr641, polyclonal, 1:1000), phospho-p38 MAPK (Thr180/Tyr182, clone D3F9, 1:1000), STAT1 (polyclonal, 1:1000), STAT3 (clone 79D7, 1:2000), STAT5 (clone D2O6Y, 1:1000, all Cell Signaling, Danvers, USA) or Dsg3 (clone 5H10, 1:1000, Bio-Techne, Minneapolis, USA), followed by detection with Dye-labeled secondary antibodies (680RD and 800CW, 1:14000, LI-COR, Lincoln, USA) for 1 h at room temperature. .. Visualization of protein bands and semi-quantitative analysis of signal intensity was performed with the Odyssey Sa infrared imaging system and Image Studio Lite software (LI-COR, Lincoln, USA).

    Article Title: IL-2/IL-2Rβγ signaling in pruriceptors drives neuroimmune mechanisms of nivolumab-induced persistent itch.
    Article Snippet: .. The membranes were blocked with 5% milk and incubated overnight at 4 °C with primary antibodies against: phospho-STAT5 (Tyr694, Cell Signaling #9359, 1:1000), total STAT5 (#94205, 1:1000), phospho-JNK (Thr183/Tyr185, Cell Signaling #4668, 1:500), total JNK (#9252, 1:1000), phospho-SHP-1 (Tyr564, Abcam ab131498, 1:500), total SHP-1 (Cell Signaling #3759, 1:1000), IL-2Rβ (CD122, R&D AF225, 1:500), IL-2Rγ (CD132, Santa Cruz sc-668, 1:200), and β-actin or GAPDH (loading controls, 1:5000). .. After washing, membranes were incubated with appropriate HRP-conjugated secondary antibodies (1:5000, Jackson Labs) for 1 h. Bands were visualized with ECL substrate (Thermo) on a ChemiDoc imager (Bio-Rad).

    Blocking Assay:

    Article Title: Translation factor eIF4G2 directs CD8 + T cell lineage commitment by selectively enabling the IL-7 receptor response
    Article Snippet: Proteins were separated by SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and transferred onto polyvinylidene difluoride (PVDF) membranes (Millipore). .. Membranes were blocked with 5% non-fat milk or bovine serum albumin (BSA) in Tris-buffered saline containing 0.1% Tween-20 (TBST) for 1 hour at room temperature and then incubated overnight at 4 °C with the following primary antibodies diluted in blocking buffer: eIF4G2 (CST, 3468S), β-actin (CST, 3700S), eIF4G1 (Proteintech, 15704-1-AP), IL-7Rα (Proteintech, 17626-1-AP), γc (Proteintech, 11409-1-AP), STAT5 (Proteintech, 13179-1-AP), phospho STAT5 (CST, 4322T), STAT6 (Proteintech, 51073-1-AP), mouse phospho STAT6 (CST, 56554S). .. After washing with TBST, membranes were incubated with horseradish peroxidase (HRP)-conjugated goat anti-mouse or anti-rabbit secondary antibody (Proteintech, SA00001-1; SA00001-9) for 1 hour at room temperature.

    Article Title: Inhibition of the JAK/STAT Signaling Pathway Suggests a Protective Effect against Acantholysis in Pemphigus
    Article Snippet: .. For specific protein identification, the membrane was blocked for 1 h at room temperature in LI-COR blocking buffer and incubated over night at 4 °C with primary antibodies recognizing actin (clone C4, 1:5000, Merck, Darmstadt, Germany or clone 13E5, 1:1000, Cell Signaling, Danvers, USA), phospho-STAT1 (Tyr701, clone 58D6, 1:1000), phospho-STAT3 (Tyr705, polyclonal, 1:1000), phospho-STAT4 (Tyr693, clone D2E4, 1:1000), phospho-STAT5 (Tyr694, clone C71E5, 1:1000), phospho-STAT6 (Tyr641, polyclonal, 1:1000), phospho-p38 MAPK (Thr180/Tyr182, clone D3F9, 1:1000), STAT1 (polyclonal, 1:1000), STAT3 (clone 79D7, 1:2000), STAT5 (clone D2O6Y, 1:1000, all Cell Signaling, Danvers, USA) or Dsg3 (clone 5H10, 1:1000, Bio-Techne, Minneapolis, USA), followed by detection with Dye-labeled secondary antibodies (680RD and 800CW, 1:14000, LI-COR, Lincoln, USA) for 1 h at room temperature. .. Visualization of protein bands and semi-quantitative analysis of signal intensity was performed with the Odyssey Sa infrared imaging system and Image Studio Lite software (LI-COR, Lincoln, USA).

    Membrane:

    Article Title: Inhibition of the JAK/STAT Signaling Pathway Suggests a Protective Effect against Acantholysis in Pemphigus
    Article Snippet: .. For specific protein identification, the membrane was blocked for 1 h at room temperature in LI-COR blocking buffer and incubated over night at 4 °C with primary antibodies recognizing actin (clone C4, 1:5000, Merck, Darmstadt, Germany or clone 13E5, 1:1000, Cell Signaling, Danvers, USA), phospho-STAT1 (Tyr701, clone 58D6, 1:1000), phospho-STAT3 (Tyr705, polyclonal, 1:1000), phospho-STAT4 (Tyr693, clone D2E4, 1:1000), phospho-STAT5 (Tyr694, clone C71E5, 1:1000), phospho-STAT6 (Tyr641, polyclonal, 1:1000), phospho-p38 MAPK (Thr180/Tyr182, clone D3F9, 1:1000), STAT1 (polyclonal, 1:1000), STAT3 (clone 79D7, 1:2000), STAT5 (clone D2O6Y, 1:1000, all Cell Signaling, Danvers, USA) or Dsg3 (clone 5H10, 1:1000, Bio-Techne, Minneapolis, USA), followed by detection with Dye-labeled secondary antibodies (680RD and 800CW, 1:14000, LI-COR, Lincoln, USA) for 1 h at room temperature. .. Visualization of protein bands and semi-quantitative analysis of signal intensity was performed with the Odyssey Sa infrared imaging system and Image Studio Lite software (LI-COR, Lincoln, USA).

    Expressing:

    Article Title: Combining lenalidomide with IL-2 family of cytokines enhances activating receptor and perforin/granzyme expression in NK cells
    Article Snippet: After assessing that the highest band transferred completely membranes were retrieved and blocked with 5% nonfat milk-based tris buffer with 0.05% Tween 20 (cat# BP337−500, Thermo Fisher Scientific, Waltham, Massachusetts, United States). .. The primary antibodies used for protein expression assessment were: total STAT5 (D3N2B, 1:1000, cat# 25656, Cell Signaling Technology, Danvers, Massachusetts, United States, RRID:AB_2798908), phospho- STAT5 (C11C5, 1:1000, cat# 9359P, Cell Signaling Technology, Danvers, Massachusetts, United States), total AKT (11E7, 1:1000, cat# 4685S, Cell Signaling Technology, Danvers, Massachusetts, United States), phospho-AKT (D25E6, 1:1000, cat# 130385, Cell Signaling Technology, Danvers, Massachusetts, United States), PI3K p85 (I9H8, 1:1000, cat# 4257, Cell Signaling Technology, Danvers, Massachusetts, United States, RRID:AB_659889) and beta-actin as a loading control (AC-74, 1:5000, cat#A5316, Sigma-Aldrich , St. Louis, Missouri, United States, RRID:AB_476743). ..

    Article Title: Combining lenalidomide with IL-2 family of cytokines enhances activating receptor and perforin/granzyme expression in NK cells.
    Article Snippet: After assessing that the highest band transferred completely membranes were retrieved and blocked with 5% nonfat milk-based tris buffer with 0.05% Tween 20 (cat# BP337−500, Thermo Fisher Scientific, Waltham, Massachusetts, United States). .. The primary antibodies used for protein expression assessment were: total STAT5 (D3N2B, 1:1000, cat# 25656, Cell Signaling Technology, Danvers, Massachusetts, United States, RRID:AB_2798908), phospho- STAT5 (C11C5, 1:1000, cat# 9359P, Cell Signaling Technology, Danvers, Massachusetts, United States), total AKT (11E7, 1:1000, cat# 4685S, Cell Signaling Technology, Danvers, Massachusetts, United States), phospho-AKT (D25E6, 1:1000, cat# 130385, Cell Signaling Technology, Danvers, Massachusetts, United States), PI3K p85 (I9H8, 1:1000, cat# 4257, Cell Signaling Technology, Danvers, Massachusetts, United States, RRID:AB_659889) and beta-actin as a loading control (AC-74, 1:5000, cat#A5316, Sigma-Aldrich, St. Louis, Missouri, United States, RRID:AB_476743). ..

    Control:

    Article Title: Combining lenalidomide with IL-2 family of cytokines enhances activating receptor and perforin/granzyme expression in NK cells
    Article Snippet: After assessing that the highest band transferred completely membranes were retrieved and blocked with 5% nonfat milk-based tris buffer with 0.05% Tween 20 (cat# BP337−500, Thermo Fisher Scientific, Waltham, Massachusetts, United States). .. The primary antibodies used for protein expression assessment were: total STAT5 (D3N2B, 1:1000, cat# 25656, Cell Signaling Technology, Danvers, Massachusetts, United States, RRID:AB_2798908), phospho- STAT5 (C11C5, 1:1000, cat# 9359P, Cell Signaling Technology, Danvers, Massachusetts, United States), total AKT (11E7, 1:1000, cat# 4685S, Cell Signaling Technology, Danvers, Massachusetts, United States), phospho-AKT (D25E6, 1:1000, cat# 130385, Cell Signaling Technology, Danvers, Massachusetts, United States), PI3K p85 (I9H8, 1:1000, cat# 4257, Cell Signaling Technology, Danvers, Massachusetts, United States, RRID:AB_659889) and beta-actin as a loading control (AC-74, 1:5000, cat#A5316, Sigma-Aldrich , St. Louis, Missouri, United States, RRID:AB_476743). ..

    Article Title: Combining lenalidomide with IL-2 family of cytokines enhances activating receptor and perforin/granzyme expression in NK cells.
    Article Snippet: After assessing that the highest band transferred completely membranes were retrieved and blocked with 5% nonfat milk-based tris buffer with 0.05% Tween 20 (cat# BP337−500, Thermo Fisher Scientific, Waltham, Massachusetts, United States). .. The primary antibodies used for protein expression assessment were: total STAT5 (D3N2B, 1:1000, cat# 25656, Cell Signaling Technology, Danvers, Massachusetts, United States, RRID:AB_2798908), phospho- STAT5 (C11C5, 1:1000, cat# 9359P, Cell Signaling Technology, Danvers, Massachusetts, United States), total AKT (11E7, 1:1000, cat# 4685S, Cell Signaling Technology, Danvers, Massachusetts, United States), phospho-AKT (D25E6, 1:1000, cat# 130385, Cell Signaling Technology, Danvers, Massachusetts, United States), PI3K p85 (I9H8, 1:1000, cat# 4257, Cell Signaling Technology, Danvers, Massachusetts, United States, RRID:AB_659889) and beta-actin as a loading control (AC-74, 1:5000, cat#A5316, Sigma-Aldrich, St. Louis, Missouri, United States, RRID:AB_476743). ..



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