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Phospho stat4

Manufactured by Cell Signaling Technology

Phospho-STAT4 is a laboratory product that detects the phosphorylated form of the STAT4 (Signal Transducer and Activator of Transcription 4) protein. STAT4 is a transcription factor that plays a key role in the signaling pathways of various cytokines, including interleukin-12 (IL-12) and type I interferons. Phosphorylation of STAT4 is an important regulatory event in these signaling cascades.

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3 protocols using phospho stat4

1

Immunoblotting Analysis of STAT Signaling

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Cell lysis, protein isolation and immunoblotting were performed as described previously [24 (link)]. Twenty micrograms of protein were resolved using 4–12% Bis-Tris polyacrylamide gels. Gels were transferred to PVDF membranes and subjected to blocking and incubation with primary and secondary antibodies. The primary antibodies used in this study included: phospho-STAT3 (Tyr705, Cell Signaling, Boston, MA and Abcam, Cambridge, MA), total STAT3 (Cell Signaling and Abcam), phospho-STAT1 (Cell Signaling), total STAT1 (Cell Signaling), phospho-STAT2 (Cell Signaling), phospho-STAT4 (Cell Signaling), phospho-STAT6 (Cell Signaling), and GAPDH (Cell Signaling). Protein bands were detected using Western Lightning ® Plus Enhanced Chemiluminescence substrate (Perkin Elmer, Waltham, MA) and HyBlot CL ® Autoradiography film (Denville Scientific, Holliston, MA). The cytokines used in this study included: interferon gamma (IFN-γ, Cell Signaling), interferon alpha (IFN-α, Cell Signaling), interleukin-4 (IL-4, Cell Signaling), interleukin-6 (IL-6, Cell Signaling), and oncostatin M (OSM, Cell Signaling).
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2

Signaling Pathway Characterization by Western Blot and Flow Cytometry

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Western blotting, cell counting kit 8 (CCK‐8), Transwell migration, and flow cytometry assays were performed as previously described (Patel et al., 2006). The primary antibodies used in this study were as follows: GAPDH (dilution 1:1000; Cell Signaling Technology, Inc.), XCR1 (dilution 1:600; Cell Signaling Technology, Inc.), JAK1 (dilution 1:600; cat. no. 2019; Cell Signaling Technology, Inc.), phospho‐JAK1 at Tyr1034/1035 (dilution 1:500; Cell Signaling Technology, Inc., JAK2 (dilution 1:1000; Cell Signaling Technology, Inc.), phospho‐JAK2 at Tyr1007 (dilution 1:1000; Cell Signaling Technology, Inc.), JAK3 (dilution 1:500; Cell Signaling Technology, Inc.), phospho‐JAK3 at Tyr980 (dilution 1:500; Cell Signaling Technology, Inc.), STAT 1–4 (dilution 1:500; dilution 1:500; Stat Antibody Sampler Kit, Cell Signaling Technology, Inc.), phospho‐STAT1 at Tyr701, phospho‐STAT2 at Tyr690, and phospho‐STAT4 at Tyr693 (dilution 1:500; Cell Signaling Technology, Inc.).
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3

Flow Cytometry of Signaling Proteins

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Cell surface or intracellular proteins (permeabilized cells) were detected by flow cytometry with fluorophore-labeled Abs to phospho-ERK, phospho-p38, phospho-JNK, phospho-IκBα, phospho-STAT1, phospho-STAT4, phospho-JAK1, phospho-JAK2, phospho-TYK2 (Cell Signaling Technology, Danvers, MA), STAT1, STAT4, IL-10RA, LC3β, and NOS2 (Santa Cruz Biotechnology, Santa Cruz, CA).
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