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mouse phospho stat6  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc mouse phospho stat6
    Mouse Phospho Stat6, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 233 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/stat6/Phospho-Stat6+(Tyr641)+Rabbit+mAb/pmc13049607-338-66-69
    Average 96 stars, based on 233 article reviews
    mouse phospho stat6 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Ubiquitin Proteomics:

    Article Title: DNA-PK-mediated phosphorylation of STAT6 establishes a non-canonical type 2 immunity axis to prevent macrophage senescence.
    Article Snippet: Then rProtein A/G Beads (Cell Signaling, # 37478) were added and incubated for 4 h. The immunoprecipitated was washed three times with buffer and followed by immunoblot. .. Antibodies used were as follows: HSP90 (Santa Cruz, #sc-13119, 1:10,000), α-Tubulin (Sigma, #T6199, 1:10,000), STAT6 (Cell Signaling, #5397, 1:1500), pSTAT6(pY641) (Cell Signaling, #56554, 1:1000), pSTAT6(pS807) (ABclonal Tech, customized, 1:200), DNA-PK (Santa Cruz, #sc-390849, 1:500), ATM (Cell Signaling, #2873, 1:1000), ATR (Santa Cruz, #sc-515173, 1:500), CHK1 (Cell Signaling, #2360, 1:1500), CHK2 (Proteintech, #13954-1-AP, 1:1000), p16-INK4A (Abcam, #ab211542, 1:1000), γH2AX (Cell Signaling, #9718, 1:1500), BRCA1 (Thermo Fisher, #MA1-23164, 1:1000), UBE2T (Thermo Fisher, #PA576202, 1:1000), JAK (Cell Signaling, #50996, 1:1000), STING (Cell Signaling, #13647, AR TI CL E IN P RE SS 1:2000), STING (pS365) (Cell Signaling, #72971, 1:1000), pTBK1 (pS172) (Cell Signaling, #5483, 1:1000), pJAK1 (pY1034/1035) (Cell Signaling, #74129, 1:1000), Ubiquitin (Cell Signaling, #3936, 1:1000), K48-specific ubiquitin (Abcam, #ab140601, 1:1000), PU.1 (Abcam, #ab227835, 1:1500), Col1a1 (Cell Signaling, #72026, 1:1000), SMAD2/3 (Cell Signaling, #8685, 1:1000), pSMAD2 (Ser465/467)/SMAD3 (Ser423/425) (Cell Signaling, #8828, 1:1000), αSMA (Cell Signaling, #19245, 1:2000) anti-HA (Cell Signaling, #3724, 1:5000) and anti-Flag (Cell Signaling, #8146, 1:5000). .. Generation of STAT6 pS807-sepicific antibody To generate a polyclonal antibody specific for STAT6 phosphorylated at Ser807 (pS807), we collaborated with ABclonal Tech.

    Article Title: DNA-PK-mediated phosphorylation of STAT6 establishes a non-canonical type 2 immunity axis to prevent macrophage senescence
    Article Snippet: Then, rProtein A/G Beads (Cell Signaling, # 37478) were added and incubated for 4 h. The immunoprecipitated was washed three times with buffer and followed by immunoblot. .. Antibodies used were as follows: HSP90 (Santa Cruz, #sc-13119, 1:10,000), α-Tubulin (Sigma, #T6199, 1:10,000), STAT6 (Cell Signaling, #5397, 1:1500), pSTAT6(pY641) (Cell Signaling, #56554, 1:1000), pSTAT6(pS807) (ABclonal Tech, customized, 1:200), DNA-PK (Santa Cruz, #sc-390849, 1:500), ATM (Cell Signaling, #2873, 1:1000), ATR (Santa Cruz, #sc-515173, 1:500), CHK1 (Cell Signaling, #2360, 1:1500), CHK2 (Proteintech, #13954-1-AP, 1:1000), p16-INK4A (Abcam, #ab211542, 1:1000), γH2AX (Cell Signaling, #9718, 1:1500), BRCA1 (Thermo Fisher, #MA1-23164, 1:1000), UBE2T (Thermo Fisher, # PA576202 , 1:1000), JAK (Cell Signaling, #50996, 1:1000), STING (Cell Signaling, #13647, 1:2000), STING (pS365) (Cell Signaling, #72971, 1:1000), pTBK1 (pS172) (Cell Signaling, #5483, 1:1000), pJAK1 (pY1034/1035) (Cell Signaling, #74129, 1:1000), Ubiquitin (Cell Signaling, #3936, 1:1000), K48-specific ubiquitin (Abcam, #ab140601, 1:1000), PU.1 (Abcam, #ab227835, 1:1500), Col1a1 (Cell Signaling, #72026, 1:1000), SMAD2/3 (Cell Signaling, #8685, 1:1000), p-SMAD2 (Ser465/467)/SMAD3 (Ser423/425) (Cell Signaling, #8828, 1:1000), αSMA (Cell Signaling, #19245, 1:2000) anti-HA (Cell Signaling, #3724, 1:5000) and anti-Flag (Cell Signaling, #8146, 1:5000). .. To generate a polyclonal antibody specific for STAT6 phosphorylated at Ser807 (pS807), we collaborated with ABclonal Tech.

    Incubation:

    Article Title: TGM2 Aggravates Acute Pancreatitis by Impairing Macrophage Efferocytosis Through Inhibition of the STAT6-GAS6 Axis.
    Article Snippet: .. The membranes were blocked with 5% skim milk at room temperature for 1 h. Primary antibodies—TGM2 (Proteintech, 15100-1-AP, 1:20000), GAS6 (Proteintech, 13795-1- P, 1:1000), STAT6 (CST, #5397, 1:1000), p-STAT6 (CST, #56554, 1:1000), p-JAK1 (CST, #3331, 1:1000) and p-JAK3 (Proteintech, 29101-1-AP, 1:1000)—were incubated overnight at 4◦C. .. After washing with PBST, fluorescent secondary antibodies (LICOR) were added and incubated at room temperature for 1 h, followed by additional washing.

    Article Title: TGM2 Aggravates Acute Pancreatitis by Impairing Macrophage Efferocytosis Through Inhibition of the STAT6-GAS6 Axis.
    Article Snippet: .. Protein samples were incubated overnight at 4◦C on a rotating shaker with IP antibodies against the following targets: TGM2 (Proteintech, 15100-1-AP, 1:50), STAT6 (Cell Signaling Technology, #5397, 1:50), and IgG (Abcam, UK, 1:50). .. Protein A/G magnetic beads (Bimake, B23202, USA) were washed three times with RIPA buffer and then blocked with 5% BSA at 4◦C for 30 min.

    Article Title: Multi-omics analysis reveals the association of cesarean delivery with altered gut microbial profiles and a Th2-biased immune response in neonates.
    Article Snippet: Equal amounts of protein were mixed with 5× loading buffer (Cat# C05-03001, Bioss, USA), denatured by heating at 95–100 °C for 5–10 min, and separated on 10% SDS-PAGE gels (Cat# SPGT001, Biolight, China). .. After electrophoresis, proteins were transferred to a membrane, blocked, and probed with primary antibodies against STAT4 (Cat# 2653T, CST, USA) and STAT6 (Cat# 5397T, CST, USA), followed by incubation with appropriate HRP-conjugated secondary antibodies. .. Protein bands were detected using ECL substrate (Cat# C05-07004, Bioss,

    Article Title: Zhi-Chuan-Ling alleviates OVA-induced allergic asthma by suppressing M2 macrophage polarization via the PI3K/AKT/mTOR/STAT6 pathway.
    Article Snippet: .. The membranes were blocked with 5 % non-fat milk at room temperature for 2 h, and then incubated with primary antibodies against the following proteins at 4 ◦C overnight: PI3K (4292, Cell Signaling Technology, MA, USA), AKT (4691, Cell Signaling Technology, MA, USA), mTOR (66,888-1-Ig, Proteintech, Wuhan, China), STAT6 (5397, Cell Signaling Technology, MA, USA), pPI3K (17,466, Cell Signaling Technology, MA, USA), p-AKT (4060, Cell Signaling Technology, MA, USA), p-mTOR (80,596-1-RR, Proteintech, Wuhan, China), and p-STAT6 (56,554, Cell Signaling Technology, MA, USA), CD206 (24,595, Cell Signaling Technology, MA, USA). ..

    Electrophoresis:

    Article Title: Multi-omics analysis reveals the association of cesarean delivery with altered gut microbial profiles and a Th2-biased immune response in neonates.
    Article Snippet: Equal amounts of protein were mixed with 5× loading buffer (Cat# C05-03001, Bioss, USA), denatured by heating at 95–100 °C for 5–10 min, and separated on 10% SDS-PAGE gels (Cat# SPGT001, Biolight, China). .. After electrophoresis, proteins were transferred to a membrane, blocked, and probed with primary antibodies against STAT4 (Cat# 2653T, CST, USA) and STAT6 (Cat# 5397T, CST, USA), followed by incubation with appropriate HRP-conjugated secondary antibodies. .. Protein bands were detected using ECL substrate (Cat# C05-07004, Bioss,

    Membrane:

    Article Title: Multi-omics analysis reveals the association of cesarean delivery with altered gut microbial profiles and a Th2-biased immune response in neonates.
    Article Snippet: Equal amounts of protein were mixed with 5× loading buffer (Cat# C05-03001, Bioss, USA), denatured by heating at 95–100 °C for 5–10 min, and separated on 10% SDS-PAGE gels (Cat# SPGT001, Biolight, China). .. After electrophoresis, proteins were transferred to a membrane, blocked, and probed with primary antibodies against STAT4 (Cat# 2653T, CST, USA) and STAT6 (Cat# 5397T, CST, USA), followed by incubation with appropriate HRP-conjugated secondary antibodies. .. Protein bands were detected using ECL substrate (Cat# C05-07004, Bioss,

    Western Blot:

    Article Title: CXCL5 suppresses osteoclastogenesis and protects against lipoteichoic acid-induced bone loss by modulating PLCγ2 and c-Fos signalling in gram-positive periprosthetic joint infection.
    Article Snippet: Protein concentrations were quantified using the BCA Protein Assay Kit (Thermo Fisher Scientific). .. Western blotting was performed using primary antibodies against the following targets: nuclear factor of activated T-cells cytoplasmic 1 (NFATc1) (4389), phospho phospholipase Cγ2 (PLCγ2) (Tyr1217, 3871T), PLCγ2 (3872T), phospho-PLCγ1 (Tyr783, 2821T), PLCγ1 (5690T), c-Fos (4384), calcineurin A (2614S), phospho-p38 mitogen-activated protein kinase (MAPK) (Thr180/Tyr182, 9211), p38 MAPK (8690), phospho-SAPK/JNK (Thr183/Tyr185, 4668), SAPK/JNK (9252), phospho-ERK1/2 (4370), ERK1/2 (9102), phospho-nuclear factor-kappa B (NF-κB) p65 (Ser536, 3033), NF-κB p65 (8242), phospho-signal transducer and activator of transcription 5 (STAT5) (Tyr694, 9359S), STAT5 (94205T), phospho-STAT6 (Tyr641, 56554S), STAT6 (5397S), phospho-FAK (Tyr397, 3283S), and FAK (3285T) (all from Cell Signaling Technology, USA); TRAP (ab191406) and CXCR2 (ab217314; Abcam); CTSK (sc-48353), tumour necrosis factor receptor-associated factor 6 (TRAF6; sc-8409), and β-actin (sc-47778; Santa Cruz Biotech nology, USA). .. Western blotting was performed using primary antibodies against the following targets: nuclear factor of activated T-cells cytoplasmic 1 (NFATc1) (4389), phospho phospholipase Cγ2 (PLCγ2) (Tyr1217, 3871T), PLCγ2 (3872T), phospho-PLCγ1 (Tyr783, 2821T), PLCγ1 (5690T), c-Fos (4384), calcineurin A (2614S), phospho-p38 mitogen-activated protein kinase (MAPK) (Thr180/Tyr182, 9211), p38 MAPK (8690), phospho-SAPK/JNK (Thr183/Tyr185, 4668), SAPK/JNK (9252), phospho-ERK1/2 (4370), ERK1/2 (9102), phospho-nuclear factor-kappa B (NF-κB) p65 (Ser536, 3033), NF-κB p65 (8242), phospho-signal transducer and activator of transcription 5 (STAT5) (Tyr694, 9359S), STAT5 (94205T), phospho-STAT6 (Tyr641, 56554S), STAT6 (5397S), phospho-FAK (Tyr397, 3283S), and FAK (3285T) (all from Cell Signaling Technology, USA); TRAP (ab191406) and CXCR2 (ab217314; Abcam); CTSK (sc-48353), tumour necrosis factor receptor-associated factor 6 (TRAF6; sc-8409), and β-actin (sc-47778; Santa Cruz Biotech nology, USA).

    Article Title: CXCL5 suppresses osteoclastogenesis and protects against lipoteichoic acid-induced bone loss by modulating PLCγ2 and c-Fos signalling in gram-positive periprosthetic joint infection
    Article Snippet: .. Western blotting was performed using primary antibodies against the following targets: nuclear factor of activated T-cells cytoplasmic 1 (NFATc1) (4389), phospho-phospholipase Cγ2 (PLCγ2) (Tyr1217, 3871T), PLCγ2 (3872T), phospho-PLCγ1 (Tyr783, 2821T), PLCγ1 (5690T), c-Fos (4384), calcineurin A (2614S), phospho-p38 mitogen-activated protein kinase (MAPK) (Thr180/Tyr182, 9211), p38 MAPK (8690), phospho-SAPK/JNK (Thr183/Tyr185, 4668), SAPK/JNK (9252), phospho-ERK1/2 (4370), ERK1/2 (9102), phospho-nuclear factor-kappa B (NF-κB) p65 (Ser536, 3033), NF-κB p65 (8242), phospho-signal transducer and activator of transcription 5 (STAT5) (Tyr694, 9359S), STAT5 (94205T), phospho-STAT6 (Tyr641, 56554S), STAT6 (5397S), phospho-FAK (Tyr397, 3283S), and FAK (3285T) (all from Cell Signaling Technology, USA); TRAP (ab191406) and CXCR2 (ab217314; Abcam); CTSK (sc-48353), tumour necrosis factor receptor-associated factor 6 (TRAF6; sc-8409), and β-actin (sc-47778; Santa Cruz Biotechnology, USA). .. Signal detection was carried out using enhanced chemiluminescence solution (Revvity, USA) and visualized with a UVP imaging system (Analytik Jena, Germany).

    Cell-Signaling:

    Article Title: CXCL5 suppresses osteoclastogenesis and protects against lipoteichoic acid-induced bone loss by modulating PLCγ2 and c-Fos signalling in gram-positive periprosthetic joint infection
    Article Snippet: .. Western blotting was performed using primary antibodies against the following targets: nuclear factor of activated T-cells cytoplasmic 1 (NFATc1) (4389), phospho-phospholipase Cγ2 (PLCγ2) (Tyr1217, 3871T), PLCγ2 (3872T), phospho-PLCγ1 (Tyr783, 2821T), PLCγ1 (5690T), c-Fos (4384), calcineurin A (2614S), phospho-p38 mitogen-activated protein kinase (MAPK) (Thr180/Tyr182, 9211), p38 MAPK (8690), phospho-SAPK/JNK (Thr183/Tyr185, 4668), SAPK/JNK (9252), phospho-ERK1/2 (4370), ERK1/2 (9102), phospho-nuclear factor-kappa B (NF-κB) p65 (Ser536, 3033), NF-κB p65 (8242), phospho-signal transducer and activator of transcription 5 (STAT5) (Tyr694, 9359S), STAT5 (94205T), phospho-STAT6 (Tyr641, 56554S), STAT6 (5397S), phospho-FAK (Tyr397, 3283S), and FAK (3285T) (all from Cell Signaling Technology, USA); TRAP (ab191406) and CXCR2 (ab217314; Abcam); CTSK (sc-48353), tumour necrosis factor receptor-associated factor 6 (TRAF6; sc-8409), and β-actin (sc-47778; Santa Cruz Biotechnology, USA). .. Signal detection was carried out using enhanced chemiluminescence solution (Revvity, USA) and visualized with a UVP imaging system (Analytik Jena, Germany).



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