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ag490 selective jak2 inhibitor  (Cayman Chemical)


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    Cayman Chemical ag490 selective jak2 inhibitor
    Ag490 Selective Jak2 Inhibitor, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ag490 selective jak2 inhibitor/product/Cayman Chemical
    Average 90 stars, based on 1 article reviews
    ag490 selective jak2 inhibitor - by Bioz Stars, 2026-05
    90/100 stars

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    EIP‐22 activates <t>JAK2/STAT3</t> signalling pathway. A, The RNA‐seq approach was used to map the transcriptome after EIP‐22 treatment in H/R model. The dysregulated genes were shown in the volcano plot, P ‐value < .05 and fold change >2. B, Heat map of the differentially expressed genes. Red indicates up‐regulation, and green indicates down‐regulation. C, KEGG pathway analysis. D, The main proteins involved in JAK2/STAT3 signalling pathway were analysed by Western blot in H/R model. E, Quantification data of Western blot analysis. F, The main proteins involved in JAK2/STAT3 signalling pathway were analysed by Western blot in H 2 O 2 model. G, Quantification data of Western blot analysis. The data represent means ± SD. ** P < .01 vs. the Scr group, *** P < .001 vs. the Scr group, # P < .05 vs. the H/R + Scr or H 2 O 2 + Scr group, ## P < .01 vs. the H/R + Scr or H 2 O 2 + Scr group
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    EIP‐22 activates <t>JAK2/STAT3</t> signalling pathway. A, The RNA‐seq approach was used to map the transcriptome after EIP‐22 treatment in H/R model. The dysregulated genes were shown in the volcano plot, P ‐value < .05 and fold change >2. B, Heat map of the differentially expressed genes. Red indicates up‐regulation, and green indicates down‐regulation. C, KEGG pathway analysis. D, The main proteins involved in JAK2/STAT3 signalling pathway were analysed by Western blot in H/R model. E, Quantification data of Western blot analysis. F, The main proteins involved in JAK2/STAT3 signalling pathway were analysed by Western blot in H 2 O 2 model. G, Quantification data of Western blot analysis. The data represent means ± SD. ** P < .01 vs. the Scr group, *** P < .001 vs. the Scr group, # P < .05 vs. the H/R + Scr or H 2 O 2 + Scr group, ## P < .01 vs. the H/R + Scr or H 2 O 2 + Scr group
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    Cayman Chemical ag490 (selective jak2 inhibitor)
    Figure 2. Effects of PI3K/AKT or <t>JAK2/STAT3</t> signaling inhibition on propofol-induced STAT3 and AKT phosphorylation. Cells were pre-incubated with different inhibitors for 30 min, and then treated with propofol for another 30 min. Cell lysates were collected and AKT and STAT3 phosphorylation was detected. ( A ) Pretreatment with wortmannin (Wort) or API-2 reduced STAT3 phosphorylation at tyr705. ( B ) Wortmannin or API-2 pretreatment reduced propofol-induced STAT3 phosphorylation at ser727. ( C and D ) Pretreatment with <t>AG490</t> or stattic inhibited propofol-induced AKT phosphorylation at ser473 and thr308. No changes in protein expression were observed with total STAT3 and total AKT in all groups ( A–D ).
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    Figure 2. Effects of PI3K/AKT or <t>JAK2/STAT3</t> signaling inhibition on propofol-induced STAT3 and AKT phosphorylation. Cells were pre-incubated with different inhibitors for 30 min, and then treated with propofol for another 30 min. Cell lysates were collected and AKT and STAT3 phosphorylation was detected. ( A ) Pretreatment with wortmannin (Wort) or API-2 reduced STAT3 phosphorylation at tyr705. ( B ) Wortmannin or API-2 pretreatment reduced propofol-induced STAT3 phosphorylation at ser727. ( C and D ) Pretreatment with <t>AG490</t> or stattic inhibited propofol-induced AKT phosphorylation at ser473 and thr308. No changes in protein expression were observed with total STAT3 and total AKT in all groups ( A–D ).
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    Figure 2. Effects of PI3K/AKT or <t>JAK2/STAT3</t> signaling inhibition on propofol-induced STAT3 and AKT phosphorylation. Cells were pre-incubated with different inhibitors for 30 min, and then treated with propofol for another 30 min. Cell lysates were collected and AKT and STAT3 phosphorylation was detected. ( A ) Pretreatment with wortmannin (Wort) or API-2 reduced STAT3 phosphorylation at tyr705. ( B ) Wortmannin or API-2 pretreatment reduced propofol-induced STAT3 phosphorylation at ser727. ( C and D ) Pretreatment with <t>AG490</t> or stattic inhibited propofol-induced AKT phosphorylation at ser473 and thr308. No changes in protein expression were observed with total STAT3 and total AKT in all groups ( A–D ).
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    Image Search Results


    EIP‐22 activates JAK2/STAT3 signalling pathway. A, The RNA‐seq approach was used to map the transcriptome after EIP‐22 treatment in H/R model. The dysregulated genes were shown in the volcano plot, P ‐value < .05 and fold change >2. B, Heat map of the differentially expressed genes. Red indicates up‐regulation, and green indicates down‐regulation. C, KEGG pathway analysis. D, The main proteins involved in JAK2/STAT3 signalling pathway were analysed by Western blot in H/R model. E, Quantification data of Western blot analysis. F, The main proteins involved in JAK2/STAT3 signalling pathway were analysed by Western blot in H 2 O 2 model. G, Quantification data of Western blot analysis. The data represent means ± SD. ** P < .01 vs. the Scr group, *** P < .001 vs. the Scr group, # P < .05 vs. the H/R + Scr or H 2 O 2 + Scr group, ## P < .01 vs. the H/R + Scr or H 2 O 2 + Scr group

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: Exercise‐induced peptide EIP‐22 protect myocardial from ischaemia/reperfusion injury via activating JAK2/STAT3 signalling pathway

    doi: 10.1111/jcmm.16441

    Figure Lengend Snippet: EIP‐22 activates JAK2/STAT3 signalling pathway. A, The RNA‐seq approach was used to map the transcriptome after EIP‐22 treatment in H/R model. The dysregulated genes were shown in the volcano plot, P ‐value < .05 and fold change >2. B, Heat map of the differentially expressed genes. Red indicates up‐regulation, and green indicates down‐regulation. C, KEGG pathway analysis. D, The main proteins involved in JAK2/STAT3 signalling pathway were analysed by Western blot in H/R model. E, Quantification data of Western blot analysis. F, The main proteins involved in JAK2/STAT3 signalling pathway were analysed by Western blot in H 2 O 2 model. G, Quantification data of Western blot analysis. The data represent means ± SD. ** P < .01 vs. the Scr group, *** P < .001 vs. the Scr group, # P < .05 vs. the H/R + Scr or H 2 O 2 + Scr group, ## P < .01 vs. the H/R + Scr or H 2 O 2 + Scr group

    Article Snippet: The AG490, a selective inhibitor of JAK2/STAT3, was purchased from Sigma Chemical Co.

    Techniques: RNA Sequencing Assay, Western Blot

    AG490 eliminates the cardioprotection of EIP‐22. A, The protein levels of p‐JAK2 and p‐STAT3 were inhibited whereas cells were treated with AG490 in H/R model. B, Quantification data of expression level of p‐JAK2 and p‐STAT3 in H/R model. C, The protein levels of p‐JAK2 and p‐STAT3 were inhibited whereas cells were treated with AG490 in H 2 O 2 model. D, Quantification data of expression level of p‐JAK2 and p‐STAT3 in H 2 O 2 model. E, The detection of cell viability in H/R model. F, The detection of cell viability in H 2 O 2 model. G, The detection of LDH level in H/R model. H, The detection of LDH level in H 2 O 2 model. I, The proteins related to apoptosis were detected in H/R model by Western blot analysis. J, Quantification data of Western blot analysis. K, The proteins related to apoptosis were detected in H 2 O 2 model by Western blot analysis. L, Quantification data of Western blot analysis. The data represent means ± SD. ** P < .01 vs. the Scr group, *** P < .001 vs. the Scr group, # P < .05 vs. the H/R + Scr or H 2 O 2 + Scr group, ## P < .01 vs. the H/R + Scr or H 2 O 2 + Scr group, & P < .05 vs. the H/R + EIP‐22 or H 2 O 2 + EIP‐22 group, && P < .01 vs. the H/R + EIP‐22 or H 2 O 2 + EIP‐22 group

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: Exercise‐induced peptide EIP‐22 protect myocardial from ischaemia/reperfusion injury via activating JAK2/STAT3 signalling pathway

    doi: 10.1111/jcmm.16441

    Figure Lengend Snippet: AG490 eliminates the cardioprotection of EIP‐22. A, The protein levels of p‐JAK2 and p‐STAT3 were inhibited whereas cells were treated with AG490 in H/R model. B, Quantification data of expression level of p‐JAK2 and p‐STAT3 in H/R model. C, The protein levels of p‐JAK2 and p‐STAT3 were inhibited whereas cells were treated with AG490 in H 2 O 2 model. D, Quantification data of expression level of p‐JAK2 and p‐STAT3 in H 2 O 2 model. E, The detection of cell viability in H/R model. F, The detection of cell viability in H 2 O 2 model. G, The detection of LDH level in H/R model. H, The detection of LDH level in H 2 O 2 model. I, The proteins related to apoptosis were detected in H/R model by Western blot analysis. J, Quantification data of Western blot analysis. K, The proteins related to apoptosis were detected in H 2 O 2 model by Western blot analysis. L, Quantification data of Western blot analysis. The data represent means ± SD. ** P < .01 vs. the Scr group, *** P < .001 vs. the Scr group, # P < .05 vs. the H/R + Scr or H 2 O 2 + Scr group, ## P < .01 vs. the H/R + Scr or H 2 O 2 + Scr group, & P < .05 vs. the H/R + EIP‐22 or H 2 O 2 + EIP‐22 group, && P < .01 vs. the H/R + EIP‐22 or H 2 O 2 + EIP‐22 group

    Article Snippet: The AG490, a selective inhibitor of JAK2/STAT3, was purchased from Sigma Chemical Co.

    Techniques: Expressing, Western Blot

    Figure 2. Effects of PI3K/AKT or JAK2/STAT3 signaling inhibition on propofol-induced STAT3 and AKT phosphorylation. Cells were pre-incubated with different inhibitors for 30 min, and then treated with propofol for another 30 min. Cell lysates were collected and AKT and STAT3 phosphorylation was detected. ( A ) Pretreatment with wortmannin (Wort) or API-2 reduced STAT3 phosphorylation at tyr705. ( B ) Wortmannin or API-2 pretreatment reduced propofol-induced STAT3 phosphorylation at ser727. ( C and D ) Pretreatment with AG490 or stattic inhibited propofol-induced AKT phosphorylation at ser473 and thr308. No changes in protein expression were observed with total STAT3 and total AKT in all groups ( A–D ).

    Journal: JAK-STAT

    Article Title: Propofol mediates signal transducer and activator of transcription 3 activation and crosstalk with phosphoinositide 3-kinase/AKT

    doi: 10.4161/jkst.29554

    Figure Lengend Snippet: Figure 2. Effects of PI3K/AKT or JAK2/STAT3 signaling inhibition on propofol-induced STAT3 and AKT phosphorylation. Cells were pre-incubated with different inhibitors for 30 min, and then treated with propofol for another 30 min. Cell lysates were collected and AKT and STAT3 phosphorylation was detected. ( A ) Pretreatment with wortmannin (Wort) or API-2 reduced STAT3 phosphorylation at tyr705. ( B ) Wortmannin or API-2 pretreatment reduced propofol-induced STAT3 phosphorylation at ser727. ( C and D ) Pretreatment with AG490 or stattic inhibited propofol-induced AKT phosphorylation at ser473 and thr308. No changes in protein expression were observed with total STAT3 and total AKT in all groups ( A–D ).

    Article Snippet: AG490 (selective JAK2 inhibitor) was purchased from Cayman Chemical.

    Techniques: Inhibition, Incubation, Expressing