dusp16 mkp7 Search Results


anti dusp16  (Proteintech)
93
Proteintech anti dusp16
Anti Dusp16, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dusp16+mkp7/DUSP16+Antibody/pmc12145754-92-34-35
Average 93 stars, based on 1 article reviews
anti dusp16 - by Bioz Stars, 2026-10
93/100 stars
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dusp16  (ABclonal Biotechnology)
94
ABclonal Biotechnology dusp16
Dusp16, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dusp16+mkp7/DUSP16+Rabbit+pAb/10__1158_slash_0008___5472__can___25___3743-119-40-41
Average 94 stars, based on 1 article reviews
dusp16 - by Bioz Stars, 2026-10
94/100 stars
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dusp16 mkp7  (OriGene)
90
OriGene dusp16 mkp7
Dusp16 Mkp7, supplied by OriGene, 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/product/dusp16+mkp7/Dusp16+(NM_130447)+Mouse+Tagged+ORF+Clone/pmc04123096-173-8-12
Average 90 stars, based on 1 article reviews
dusp16 mkp7 - by Bioz Stars, 2026-10
90/100 stars
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dusp16  (Cell Signaling Technology Inc)
90
Cell Signaling Technology Inc dusp16
Fig. 5 FBXL18 targeted <t>DUSP16</t> as a ubiquitination substrate. (A-B) The results of Co-IP and western blotting assays revealed the endogenous and exog enous interaction of FBXL18 and DUSP16. (C-D) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. (E-F) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. (G-H) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. (I-J) DUSP16 protein half-life in EC cells of LV-Control and LV- FBXL18 groups were evaluated by CHX chase assay. (K-L) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. (M-N) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. *P < 0.05; **P < 0.01; ***P < 0.001
Dusp16, supplied by Cell Signaling Technology Inc, 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/product/dusp16+mkp7/DUSP16%2FMKP7+Rabbit+mAb/pm40382593-100-10-12
Average 90 stars, based on 1 article reviews
dusp16 - by Bioz Stars, 2026-10
90/100 stars
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mapk phosphatase dusp16/mkp-7  (KU Leuven)
90
KU Leuven mapk phosphatase dusp16/mkp-7
Fig. 5 FBXL18 targeted <t>DUSP16</t> as a ubiquitination substrate. (A-B) The results of Co-IP and western blotting assays revealed the endogenous and exog enous interaction of FBXL18 and DUSP16. (C-D) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. (E-F) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. (G-H) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. (I-J) DUSP16 protein half-life in EC cells of LV-Control and LV- FBXL18 groups were evaluated by CHX chase assay. (K-L) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. (M-N) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. *P < 0.05; **P < 0.01; ***P < 0.001
Mapk Phosphatase Dusp16/Mkp 7, supplied by KU Leuven, 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/product/dusp16+mkp7/mapk+phosphatase+dusp16+mkp+7/pm14586399-1-4-38
Average 90 stars, based on 1 article reviews
mapk phosphatase dusp16/mkp-7 - by Bioz Stars, 2026-10
90/100 stars
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anti-mkp-7 dusp16 antibody  (Boster Bio)
N/A
Boster Bio Anti-MKP-7 DUSP16 Antibody catalog # A06264-1. Tested in ELISA, IF, IHC, WB applications. This antibody reacts with Human, Mouse.
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dusp16 mkp7 antibody  (Abcepta)
N/A
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Image Search Results


Fig. 5 FBXL18 targeted DUSP16 as a ubiquitination substrate. (A-B) The results of Co-IP and western blotting assays revealed the endogenous and exog enous interaction of FBXL18 and DUSP16. (C-D) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. (E-F) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. (G-H) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. (I-J) DUSP16 protein half-life in EC cells of LV-Control and LV- FBXL18 groups were evaluated by CHX chase assay. (K-L) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. (M-N) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. *P < 0.05; **P < 0.01; ***P < 0.001

Journal: Cancer cell international

Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.

doi: 10.1186/s12935-025-03808-9

Figure Lengend Snippet: Fig. 5 FBXL18 targeted DUSP16 as a ubiquitination substrate. (A-B) The results of Co-IP and western blotting assays revealed the endogenous and exog enous interaction of FBXL18 and DUSP16. (C-D) qRT-PCR analysis of DUSP16 mRNA levels after silencing or overexpressing FBXL18 in KLE and Ishikawa cells. (E-F) Western blot analysis of DUSP16 protein level in EC cells of shNC and shFBXL18 groups, and quantitative analysis. (G-H) Western blot analysis of DUSP16 protein level in EC cells after overexpressing FBXL18, and quantitative analysis. (I-J) DUSP16 protein half-life in EC cells of LV-Control and LV- FBXL18 groups were evaluated by CHX chase assay. (K-L) Comparison of DUSP16 protein half-life in EC cells stably knockdown of FBXL18 and control cells. (M-N) The ubiquitination status of endogenous DUSP16 after silencing or overexpressing FBXL18 in EC cells were determined by immunoprecipitation and western blotting. *P < 0.05; **P < 0.01; ***P < 0.001

Article Snippet: The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

Techniques: Ubiquitin Proteomics, Co-Immunoprecipitation Assay, Western Blot, Quantitative RT-PCR, Control, Comparison, Stable Transfection, Knockdown, Immunoprecipitation

Fig. 7 Silence of FBXL18 inhibited EC growth in vivo. (A) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. (B) Representative images of xenograft tumors in shNC and shFBXL18 groups. (C) Tumor weights of shNC and shFBXL18 groups were measured at the end point. (E) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. (F) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. *P < 0.05; **P < 0.01; ***P < 0.001

Journal: Cancer cell international

Article Title: FBXL18 promotes endometrial carcinoma progression via destabilizing DUSP16 and thus activating JNK signaling pathway.

doi: 10.1186/s12935-025-03808-9

Figure Lengend Snippet: Fig. 7 Silence of FBXL18 inhibited EC growth in vivo. (A) Tumor volumes of shNC and shFBXL18 groups were determined at different defined time points. (B) Representative images of xenograft tumors in shNC and shFBXL18 groups. (C) Tumor weights of shNC and shFBXL18 groups were measured at the end point. (E) Western blot analysis of FBXL18, DUSP16, JNK, p-JNK, c-JUN, p-c-JUN, and EMT-related markers in tumor samples of shNC and shFBXL18 groups, and quantitative analysis. (F) qRT-PCR analysis of FBXL18 and DUSP16 in tumor samples of shNC and shFBXL18 groups. *P < 0.05; **P < 0.01; ***P < 0.001

Article Snippet: The primary antibodies included FBXL18 (sc-100738, Santa Cruz, USA; 1:500), DUSP16 (#5523, CST, USA; 1:1000), GAPDH (GB15004100, Servicebio, China; 1:500), JNK (#9252, CST, USA; 1:1000), p-JNK (#9251, CST, USA; 1:500), c-Jun (#9165, CST, USA; 1:1000), and p-c-Jun (#3270, CST, USA; 1:1000).

Techniques: In Vivo, Western Blot, Quantitative RT-PCR