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rabbit anti human p jak2  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti human p jak2
    Rabbit Anti Human P Jak2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 146 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+human+p+jak2/ppr0835000-91-57-61?v=Cell+Signaling+Technology+Inc
    Average 95 stars, based on 146 article reviews
    rabbit anti human p jak2 - by Bioz Stars, 2026-07
    95/100 stars

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    rabbit anti human jak2 p jak2 monoclonal antibody  (Cell Signaling Technology Inc)
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    Figure 7. Role of IL-8 signaling in EMT. (A) The expression of <t>Jak2,</t> p-Jak2, Stat3, p-Stat3 and Snail were assessed in Hep-G2 exposure to different concentrations of IL-8. (B-D) Semi-quantitative analysis demonstrated that Jak2/Stat3/Snail pathway could be activated by IL-8. (#p>0.05; *p<0.05). (E) Immunofluorescent analysis of E-Cadherin, N-Cadherin and Snail in Hep-G2 vs. Hep-G2 that was incubated with IL-8. The green signal represents the staining of the corresponding protein and the blue signal represents the DAPI-stained nuclei. The morphological change of Hep-G2 after incubated with IL-8 was also observed. (F and G) Functional analysis is illustrated after IL-8 had been added to the media for 24 h. A transwell assay showed that the number of invading Hep-G2 cells were higher that in control groups (original magnification, x100).
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    Figure 7. Role of IL-8 signaling in EMT. (A) The expression of Jak2, p-Jak2, Stat3, p-Stat3 and Snail were assessed in Hep-G2 exposure to different concentrations of IL-8. (B-D) Semi-quantitative analysis demonstrated that Jak2/Stat3/Snail pathway could be activated by IL-8. (#p>0.05; *p<0.05). (E) Immunofluorescent analysis of E-Cadherin, N-Cadherin and Snail in Hep-G2 vs. Hep-G2 that was incubated with IL-8. The green signal represents the staining of the corresponding protein and the blue signal represents the DAPI-stained nuclei. The morphological change of Hep-G2 after incubated with IL-8 was also observed. (F and G) Functional analysis is illustrated after IL-8 had been added to the media for 24 h. A transwell assay showed that the number of invading Hep-G2 cells were higher that in control groups (original magnification, x100).

    Journal: International journal of oncology

    Article Title: Macrophage-secreted IL-8 induces epithelial-mesenchymal transition in hepatocellular carcinoma cells by activating the JAK2/STAT3/Snail pathway.

    doi: 10.3892/ijo.2014.2761

    Figure Lengend Snippet: Figure 7. Role of IL-8 signaling in EMT. (A) The expression of Jak2, p-Jak2, Stat3, p-Stat3 and Snail were assessed in Hep-G2 exposure to different concentrations of IL-8. (B-D) Semi-quantitative analysis demonstrated that Jak2/Stat3/Snail pathway could be activated by IL-8. (#p>0.05; *p<0.05). (E) Immunofluorescent analysis of E-Cadherin, N-Cadherin and Snail in Hep-G2 vs. Hep-G2 that was incubated with IL-8. The green signal represents the staining of the corresponding protein and the blue signal represents the DAPI-stained nuclei. The morphological change of Hep-G2 after incubated with IL-8 was also observed. (F and G) Functional analysis is illustrated after IL-8 had been added to the media for 24 h. A transwell assay showed that the number of invading Hep-G2 cells were higher that in control groups (original magnification, x100).

    Article Snippet: Rabbit anti-human JAK2/p-JAK2 monoclonal antibody (1:1,000; 3230; Cell Signaling Technology, Danvers, MA, uSA/1:1,000; 4406; Cell Signaling Technology) and rabbit anti-human STAT3/p-STAT3 monoclonal antibody (1:1,000; 4904; Cell Signaling Technology/1:2,000; 9145; Cell Signaling Technology) were selected to detect the JAK2/STAT3 pathway.

    Techniques: Expressing, Incubation, Staining, Functional Assay, Transwell Assay, Control