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Miltenyi Biotec
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R&D Systems
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Immunotec inc
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Miltenyi Biotec
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Millipore
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Journal: World Journal of Surgical Oncology
Article Title: CD55 may be an important prognostic factor of thymic epithelial tumors: a retrospective study
doi: 10.1186/s12957-025-04051-2
Figure Lengend Snippet: Expression of CD55 mRNA and protein in normal thymus, thymoma, and TSCC. The expression levels of CD55 mRNA ( A ) and protein ( B ) were significantly elevated progressively in normal thymus tissue, thymoma, and TSCC
Article Snippet: The primary
Techniques: Expressing
Journal: World Journal of Surgical Oncology
Article Title: CD55 may be an important prognostic factor of thymic epithelial tumors: a retrospective study
doi: 10.1186/s12957-025-04051-2
Figure Lengend Snippet: Intensities of CD55 expression in TETs (IHC) scored 0: negative expression ( A , 40×; a, 200×); scored 1: low expression ( B , 40×; b, 200×); scored 2: moderate expression ( C , 40×; c, 200×); scored 3: high expression ( D , 40×; d, 200×)
Article Snippet: The primary
Techniques: Expressing
Journal: World Journal of Surgical Oncology
Article Title: CD55 may be an important prognostic factor of thymic epithelial tumors: a retrospective study
doi: 10.1186/s12957-025-04051-2
Figure Lengend Snippet: Proportion of CD55 expression in TETs (IHC) scored 0: negative expression ( A , 40×; a, 200×); scored 1: 1% − 30% positive cells ( B , 40×; b, 200×); scored 2: 30% − 60% positive cells ( C , 40×; c, 200×); scored 3: ≥ 60% positive cells ( D , 40×; d, 200×)
Article Snippet: The primary
Techniques: Expressing
Journal: World Journal of Surgical Oncology
Article Title: CD55 may be an important prognostic factor of thymic epithelial tumors: a retrospective study
doi: 10.1186/s12957-025-04051-2
Figure Lengend Snippet: Kaplan-Meier Survival Analysis in TETs The results demonstrated that PFS of TETs was closely related to CD55 mRNA ( A , p < 0.0001), CD55 protein ( B , p < 0.0001), tumor completeness of resection ( C , p < 0.0001), histological type ( D , p < 0.0001), Masaoka-Koga stage ( E , p < 0.0001), and adjuvant therapy ( F , p = 0.0009), but no with gender ( G , p = 0.1805) or MG ( H , p = 0.7269)
Article Snippet: The primary
Techniques: Adjuvant
Journal: World Journal of Surgical Oncology
Article Title: CD55 may be an important prognostic factor of thymic epithelial tumors: a retrospective study
doi: 10.1186/s12957-025-04051-2
Figure Lengend Snippet: The relationship between CD55 and the clinical pathological features of patients The expression levels of CD55 mRNA and protein were higher in R1/R2 group ( A ), higher histological grade ( B ), Masaoka-Koga stage III/IV ( C ), adjuvant therapy ( D ) compared with the corresponding R0 group, normal thymus tissues, and stage I/II, and no-adjuvant therapy. Moreover, the expression of CD55 protein was significantly higher expressed in ≥ 60 years compared with ˂60 years ( E ). Additionally, CD55 protein expression was higher in males than that in females ( F ), whereas CD55 mRNA did not show similar results ( E, F ). Patients without MG showed higher CD55 mRNA and protein expression levels than those with MG, however, this difference was not statistically significant ( G ). There was also no statistically significant relationship between tumor diameter and CD55 expression ( H ). When CD55 protein was highly expressed, the mRNA level was also high ( I ).
Article Snippet: The primary
Techniques: Expressing, Adjuvant
Journal: World Journal of Surgical Oncology
Article Title: CD55 may be an important prognostic factor of thymic epithelial tumors: a retrospective study
doi: 10.1186/s12957-025-04051-2
Figure Lengend Snippet: Kaplan-Meier Survival Analysis in high-risk TETs The results demonstrated that PFS of high-risk TETs was closely related to high expression of CD55 mRNA (A, p < 0.0001) and CD55 protein (B, p = 0.0168)
Article Snippet: The primary
Techniques: Expressing
Journal: Pathogens
Article Title: Relationship Between Cell Surface Viral Glycoprotein Expression and Resistance of Parainfluenza Virus Persistently Infected Cells to Complement-Mediated Lysis
doi: 10.3390/pathogens14080815
Figure Lengend Snippet: C′ regulators are not significantly upregulated in H1975 and HEp2 PI cells. ( A , B ) RNA samples from H1975 ( A ) and HEp2 ( B ) cells were collected as described in the legend to . Samples were analyzed via RT-qPCR to determine gene expression of three C′ regulators: CD46, CD55, and CFH. Values were normalized to expression of β-actin. C′ inhibitor expression in mock-infected cell cultures was set equal to 1 and expression in AI and PI cel cultures is expressed as fold change relative to mock. ( C ) Mock-infected, AI, and PI HEp2 cells were stained with an anti-CD55 antibody and processed via flow cytometry. MFI; Mean Fluorescence Intensity. ns stands for not significant, **** indicates p -value < 0.0001.
Article Snippet: CD55 surface expression was monitored using an
Techniques: Quantitative RT-PCR, Gene Expression, Expressing, Infection, Staining, Flow Cytometry, Fluorescence
Journal: International Journal of Molecular Sciences
Article Title: Complement-Mediated Two-Step NETosis: Serum-Induced Complement Activation and Calcium Influx Generate NADPH Oxidase-Dependent NETs in Serum-Free Conditions
doi: 10.3390/ijms25179625
Figure Lengend Snippet: Complement activation increases complement regulators on neutrophils. Neutrophils were precoated with anti-CD59 monoclonal antibodies and then exposed to normal human serum (NHS) to activate the complement cascade (complement stimulated). The group not treated with anti-CD59 monoclonal antibodies served as the unstimulated control (serum). The cells were then fixed, immunostained, and analyzed by flow cytometry. The expression level of all three complement regulators (CD46, CD55, and CD59) was significantly increased on complement-activated neutrophils compared to the unstimulated controls. ( A ) Representative flow cytometry tracings of an experiment; ( B ) mean fluorescence intensity (MFI) for each marker from all experiments. n = 3 biological replicates. * p < 0.05, compared to their controls, based on the paired t-test. Data are presented as means ± SD.
Article Snippet: To specifically deactivate the complement activity of serum, while leaving other serum proteins functional, serum was heated for 56 degrees Celsius for 30 min. Primary antibodies C3b (1:500; Mouse, ThermoFisher Invitrogen, Carlsbad, CA, USA; Cat# MA1-70054), C5b-9 (1:250, Rabbit, Abcam, Toronto, ON, Canada; Cat# Ab55811), CD46 (1:200, Rabbit, Santa Cruz Biotech, Dallas, TX, USA; Cat# SC 9098),
Techniques: Activation Assay, Bioprocessing, Control, Flow Cytometry, Expressing, Fluorescence, Marker