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anti phosphor stat6tyr641  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti phosphor stat6tyr641
    Anti Phosphor Stat6tyr641, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 396 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti phosphor stat6tyr641/product/Cell Signaling Technology Inc
    Average 96 stars, based on 396 article reviews
    anti phosphor stat6tyr641 - by Bioz Stars, 2026-03
    96/100 stars

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    Cell Signaling Technology Inc phosphor stat6 tyr641
    liposomal honokiol (Lip-HNK) regulates M1/M2 polarization via the STAT1/6 pathway. Interferon γ (IFN-γ) (20 ng/mL) and lipopolysaccharide (LPS) (10 ng/mL) with Lip-HNK were used to treat RAW264.7 (A) and BV2 (B) cells for 48 hours. p-STAT1, activators of transcription (STAT1), and signal transducers p(Y701)-STAT1, p(S727)-STAT1, STAT1 were evaluated by Western blot. RAW264.7 (C) and BV2 (D) cells were treated with interleukin 4 (IL-4) (20 ng/mL) and indicated concentrations of Lip-HNK. <t>p-STAT6</t> and STAT6 were evaluated using Western blot analysis. The 3 independent experiments are illustrated by histogram bars. The data are displayed as the mean ± standard deviation. *, P<0.05; **, P<0.01; ***, P<0.001. #, P<0.05; ##, P<0.01.
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    Cell Signaling Technology Inc phosphor ylation stat6
    liposomal honokiol (Lip-HNK) regulates M1/M2 polarization via the STAT1/6 pathway. Interferon γ (IFN-γ) (20 ng/mL) and lipopolysaccharide (LPS) (10 ng/mL) with Lip-HNK were used to treat RAW264.7 (A) and BV2 (B) cells for 48 hours. p-STAT1, activators of transcription (STAT1), and signal transducers p(Y701)-STAT1, p(S727)-STAT1, STAT1 were evaluated by Western blot. RAW264.7 (C) and BV2 (D) cells were treated with interleukin 4 (IL-4) (20 ng/mL) and indicated concentrations of Lip-HNK. <t>p-STAT6</t> and STAT6 were evaluated using Western blot analysis. The 3 independent experiments are illustrated by histogram bars. The data are displayed as the mean ± standard deviation. *, P<0.05; **, P<0.01; ***, P<0.001. #, P<0.05; ##, P<0.01.
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    liposomal honokiol (Lip-HNK) regulates M1/M2 polarization via the STAT1/6 pathway. Interferon γ (IFN-γ) (20 ng/mL) and lipopolysaccharide (LPS) (10 ng/mL) with Lip-HNK were used to treat RAW264.7 (A) and BV2 (B) cells for 48 hours. p-STAT1, activators of transcription (STAT1), and signal transducers p(Y701)-STAT1, p(S727)-STAT1, STAT1 were evaluated by Western blot. RAW264.7 (C) and BV2 (D) cells were treated with interleukin 4 (IL-4) (20 ng/mL) and indicated concentrations of Lip-HNK. p-STAT6 and STAT6 were evaluated using Western blot analysis. The 3 independent experiments are illustrated by histogram bars. The data are displayed as the mean ± standard deviation. *, P<0.05; **, P<0.01; ***, P<0.001. #, P<0.05; ##, P<0.01.

    Journal: Annals of Translational Medicine

    Article Title: Liposomal honokiol inhibits glioblastoma growth through regulating macrophage polarization

    doi: 10.21037/atm-21-1836

    Figure Lengend Snippet: liposomal honokiol (Lip-HNK) regulates M1/M2 polarization via the STAT1/6 pathway. Interferon γ (IFN-γ) (20 ng/mL) and lipopolysaccharide (LPS) (10 ng/mL) with Lip-HNK were used to treat RAW264.7 (A) and BV2 (B) cells for 48 hours. p-STAT1, activators of transcription (STAT1), and signal transducers p(Y701)-STAT1, p(S727)-STAT1, STAT1 were evaluated by Western blot. RAW264.7 (C) and BV2 (D) cells were treated with interleukin 4 (IL-4) (20 ng/mL) and indicated concentrations of Lip-HNK. p-STAT6 and STAT6 were evaluated using Western blot analysis. The 3 independent experiments are illustrated by histogram bars. The data are displayed as the mean ± standard deviation. *, P<0.05; **, P<0.01; ***, P<0.001. #, P<0.05; ##, P<0.01.

    Article Snippet: Antibodies against the following proteins were used: phosphor-STAT1 Tyr701 , phosphor-STAT1 ser727 , STAT1, STAT6, phosphor-STAT6 Tyr641 , and GAPDH (Cat. #8826, #9167, #14994, #56554, #5397, and #5174, respectively, Cell Signaling Technology, USA).

    Techniques: Western Blot, Standard Deviation