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12282s  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc 12282s
    12282s, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1192 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cox2/Cox2+XP+Rabbit+mAb/pm42849665-97-36-37
    Average 97 stars, based on 1192 article reviews
    12282s - by Bioz Stars, 2026-10
    97/100 stars

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    Related Articles

    Incubation:

    Article Title: Apigenin Attenuates LPS-Induced Corneal Inflammation by Modulating NF-κB and JNK/ERK Signaling Pathways.
    Article Snippet: 12 Objective: To investigate the protective effects and molecular mechanisms of 13 apigenin (API) on lipopolysaccharide (LPS)-induced corneal inflammation.. 14 Methods: Immortalized human corneal epithelial cell line (HCECs) and primary 15 human corneal epithelial cells (PHCECs) were used to establish LPS-induced 16 inflammation models in vitro.. IL-6 and IL-8 mRNA and protein levels were assessed 17 by qRT-PCR and ELISA.

    Article Title: PrP C Glycoprotein Modulates Atmospherically Relevant Artificial Particulate Matter-Induced Development of Lung Cancer in Mice.
    Article Snippet: .. Tissue slides were incubated overnight at 4 °C with specific antibodies, including c-Myc (sc-42-Santa Cruz Biotechnology), Sox2 (sc-365823-Santa Cruz Biotechnology), TTF1 (sc-53136-Santa Cruz Biotechnology), K-ras (TA801672-Origene), Ki67 (ab16667-abcam), CK7 (ET1609-63 Huabio), PrPC (A03202-SPI bio), HIF-1α (NB100-449-Novus Biologicals), COX2 (BS1076-BioWord), IL-1β (sc52012-Santa Cruz Biotechnology), TNFα (AB1793-Abcam), 8- OHdG (Ab62623-Abcam), CD4 (25229-Cell Signaling), CD8 (sc7970-Santa Cruz Biotechnology) and VEGF-A (BS2853-Bio World). https://doi.org/10.1021/acs.est.5c08365 Environ. ..

    Western Blot:

    Article Title: Circular RNA circATM binds PARP1 to suppress Wnt/β-catenin signaling and induce cell cycle arrest in gastric cancer cells
    Article Snippet: The following antibodies were used in the Co-IP assay: anti-FLAG M2 antibody (Sigma-Aldrich Cat# F1804, RRID:AB_262044), anti-PARP1 antibody (Proteintech Cat# 66520-1-Ig, RRID:AB_2881883), anti-β-catenin antibody (Cell Signaling Technology Cat# 8480, RRID:AB_11127855), rabbit IgG (Cell Signaling Technology Cat# 3900, RRID:AB_1550038), and mouse IgG (Cell Signaling Technology Cat# 5415, RRID:AB_10829607). .. Antibodies targeting the following markers were used for western blotting: PARP (Cell Signaling Technology Cat# 9542, RRID:AB_2160739), Survivin (Cell Signaling Technology Cat# 2808, RRID:AB_2063948), Cox2 (Cell Signaling Technology Cat# 4842, RRID:AB_2084968), APC (Cell Signaling Technology Cat# 2504, RRID:AB_2057484), AXIN2 (Cell Signaling Technology Cat# 5863, RRID:AB_10835211), TCF4 (Cell Signaling Technology Cat# 2953, RRID:AB_2199265), p16 (Cell Signaling Technology Cat# 92803, RRID:AB_2750891), p21 (Cell Signaling Technology Cat# 2947, RRID:AB_823586), p27 (Cell Signaling Technology Cat# 3686, RRID:AB_2077850), CDK2 (Cell Signaling Technology Cat# 2546, RRID:AB_2276129), cyclin A2 (Cell Signaling Technology Cat# 4656, RRID:AB_2071958), ATM (Cell Signaling Technology Cat# 2873, RRID:AB_2062659), phospho-ATM (Ser1,981) (Cell Signaling Technology Cat# 4526, RRID:AB_2062663), Chk1 (Cell Signaling Technology Cat# 2360, RRID:AB_2080320), phospho-Chk1 (Cell Signaling Technology Cat# 2348, RRID:AB_331212), Chk2 (Cell Signaling Technology Cat# 6334, RRID:AB_11178526), phospho-Chk2 (Cell Signaling Technology Cat# 2197, RRID:AB_2080501), GAPDH (Cell Signaling Technology Cat# 5174, RRID:AB_10622025), cyclin D1, c-Jun, c-Myc, c-Met in the Wnt/β-catenin Activated Targets Antibody Sampler Kit (#8655), and γH2AX (S139) (Abcam Cat# ab81299, RRID:AB_1640564). .. Total RNA was extracted from the GC samples using the Eastep TM Super Total RNA Extraction Kit (Cat. LS1040, Promega, Beijing, China).

    Article Title: The engineered probiotic strain Lactococcus lactis MG1363-pMG36e-GLP-1 regulates microglial polarization and gut dysbiosis in a transgenic mouse model of Parkinson’s disease
    Article Snippet: iNOS , Rabbit , 1:2000 , Proteintech , 18985-1-AP , AB_2934933 , Western blotting. .. COX2 , Rabbit , 1:1000 , CST , 12282S , AB_2084968 , Western blotting. .. GLP-1R , Rabbit , 1:1000 , Proteintech , 26196-1-AP , AB_2880421 , Western blotting.



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    Therapeutic effect of LAC in the monoiodoacetate mouse model. (A) H&E staining of the joint from MIA mice after different treatments. (B) Quantitative analysis of the synovitis score. (C) Representative images of SO&FG‐stained knee joint sections from MIA mice with different treatments. (D) The severity of OA‐like lesions was analyzed using the OARSI scoring system. (E) Immunofluorescence imaging of iNOS (red)/CD206 (green) within the knee joints of mice with different treatments. (F) Corresponding quantification of the MFI of CD206 in the synovium of mice with different treatments. (G) Immunohistochemical staining of <t>COX‐2,</t> TNF‐α, and TRAP in the knee joints of mice with different treatments. (H,I) Quantification of the relative density of COX‐2 + (H) and TNF‐α + (I) cells in the knee joints of mice with different treatments. n = 5 in B and D, and n = 3 in F, H, and I, mean ± SD. The significant differences are determined by one‐way ANOVA analysis with Tukey's multiple comparison test. ** p < 0.01, *** p < 0.001, **** p < 0.0001, ns stands for no significant difference.
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    Upregulation of proteins associated with uterine TLR2/4–NF-κB–COX-2 inflammatory signaling in rats with Gardnerella vaginalis -associated bacterial vaginosis. (A) Relative protein abundance of Toll-like receptor 2 (TLR2), TLR4, phospho-NF-κB p65 at serine 536 (pS536-p65) <t>and</t> <t>cyclooxygenase-2</t> (COX-2) in uterine tissues. Data are presented as the means ( X ¯ ) ± standard error of the mean (SEM); n = 3 independent uterine tissue samples per group. Statistical significance was determined using Student’s t-tests . Complete densitometric values are provided in <xref ref-type=Supplementary Table 11 . (B) Representative Western blot images. Protein levels were normalized to glyceraldehyde-3-phosphate dehydrogenase (GAPDH). Original uncropped Western blot images are provided in Supplementary Figure 1 . " width="250" height="auto" />
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    Image Search Results


    Therapeutic effect of LAC in the monoiodoacetate mouse model. (A) H&E staining of the joint from MIA mice after different treatments. (B) Quantitative analysis of the synovitis score. (C) Representative images of SO&FG‐stained knee joint sections from MIA mice with different treatments. (D) The severity of OA‐like lesions was analyzed using the OARSI scoring system. (E) Immunofluorescence imaging of iNOS (red)/CD206 (green) within the knee joints of mice with different treatments. (F) Corresponding quantification of the MFI of CD206 in the synovium of mice with different treatments. (G) Immunohistochemical staining of COX‐2, TNF‐α, and TRAP in the knee joints of mice with different treatments. (H,I) Quantification of the relative density of COX‐2 + (H) and TNF‐α + (I) cells in the knee joints of mice with different treatments. n = 5 in B and D, and n = 3 in F, H, and I, mean ± SD. The significant differences are determined by one‐way ANOVA analysis with Tukey's multiple comparison test. ** p < 0.01, *** p < 0.001, **** p < 0.0001, ns stands for no significant difference.

    Journal: Exploration

    Article Title: Soluble Nanomedicine Against Soluble Neurosensitizers to Effectively Relieve Osteoarthritis Pain and Joint Damage

    doi: 10.1002/exp2.70233

    Figure Lengend Snippet: Therapeutic effect of LAC in the monoiodoacetate mouse model. (A) H&E staining of the joint from MIA mice after different treatments. (B) Quantitative analysis of the synovitis score. (C) Representative images of SO&FG‐stained knee joint sections from MIA mice with different treatments. (D) The severity of OA‐like lesions was analyzed using the OARSI scoring system. (E) Immunofluorescence imaging of iNOS (red)/CD206 (green) within the knee joints of mice with different treatments. (F) Corresponding quantification of the MFI of CD206 in the synovium of mice with different treatments. (G) Immunohistochemical staining of COX‐2, TNF‐α, and TRAP in the knee joints of mice with different treatments. (H,I) Quantification of the relative density of COX‐2 + (H) and TNF‐α + (I) cells in the knee joints of mice with different treatments. n = 5 in B and D, and n = 3 in F, H, and I, mean ± SD. The significant differences are determined by one‐way ANOVA analysis with Tukey's multiple comparison test. ** p < 0.01, *** p < 0.001, **** p < 0.0001, ns stands for no significant difference.

    Article Snippet: Proteins in equivalent amounts were then separated on a 10% sodium dodecyl sulfate‐polyacrylamide gel electrophoresis (SDS‐PAGE) and transferred to the PVDF membrane, followed by blocking in TBS‐T solution containing 5% skim milk for 1 h. Subsequently, the membrane was incubated with primary antibody against COX‐2 (66351‐1‐Ig, Proteintech), iNOS (80517‐1‐RR, Proteintech), and CD206 (60143‐1‐Ig, Proteintech) overnight at 4°C.

    Techniques: Staining, Analysis, Immunofluorescence, Imaging, Immunohistochemical staining, Comparison

    Upregulation of proteins associated with uterine TLR2/4–NF-κB–COX-2 inflammatory signaling in rats with Gardnerella vaginalis -associated bacterial vaginosis. (A) Relative protein abundance of Toll-like receptor 2 (TLR2), TLR4, phospho-NF-κB p65 at serine 536 (pS536-p65) and cyclooxygenase-2 (COX-2) in uterine tissues. Data are presented as the means ( X ¯ ) ± standard error of the mean (SEM); n = 3 independent uterine tissue samples per group. Statistical significance was determined using Student’s t-tests . Complete densitometric values are provided in <xref ref-type=Supplementary Table 11 . (B) Representative Western blot images. Protein levels were normalized to glyceraldehyde-3-phosphate dehydrogenase (GAPDH). Original uncropped Western blot images are provided in Supplementary Figure 1 . " width="100%" height="100%">

    Journal: Frontiers in Immunology

    Article Title: Inflammatory landscape of Gardnerella vaginalis -associated bacterial vaginosis in rats: an integrated multi-omics analysis

    doi: 10.3389/fimmu.2026.1914434

    Figure Lengend Snippet: Upregulation of proteins associated with uterine TLR2/4–NF-κB–COX-2 inflammatory signaling in rats with Gardnerella vaginalis -associated bacterial vaginosis. (A) Relative protein abundance of Toll-like receptor 2 (TLR2), TLR4, phospho-NF-κB p65 at serine 536 (pS536-p65) and cyclooxygenase-2 (COX-2) in uterine tissues. Data are presented as the means ( X ¯ ) ± standard error of the mean (SEM); n = 3 independent uterine tissue samples per group. Statistical significance was determined using Student’s t-tests . Complete densitometric values are provided in Supplementary Table 11 . (B) Representative Western blot images. Protein levels were normalized to glyceraldehyde-3-phosphate dehydrogenase (GAPDH). Original uncropped Western blot images are provided in Supplementary Figure 1 .

    Article Snippet: After blocking with a rapid blocking buffer (Epizyme, Shanghai, China), the blots were incubated overnight at 4 °C with the following primary antibodies: TLR2 (Abcam, Cambridge, UK; dilution 1:1000), TLR4 (Proteintech, Hubei, China; dilution 1:1000), phospho-NF-κB p65 at serine 536 (pS536-p65; Proteintech; dilution 1:2000), cyclooxygenase-2 (COX-2; Proteintech; dilution 1:1000), and glyceraldehyde-3-phosphate dehydrogenase (GAPDH; Proteintech; dilution 1:10000).

    Techniques: Quantitative Proteomics, Tissue, Western Blot