thymoma tissue microarray Search Results


thymoma tissue microarray  (Purdue University Cytometry)
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Purdue University Cytometry thymoma tissue microarray
IHC was performed on a BioMax multi-cancer tissue <t>microarray</t> using the FR-β specific monoclonal antibody m909. The relative staining intensity, graded on a scale of 0 to 3, of positively staining cells within the tumor and stroma were determined. A ) Statistically significant differences ( p -value <0.05) using ANOVA or a t-test and correlations using a Spearman correlation ( p -value <0.05) between the average FR-β staining intensity and various pathological data are summarized. B ) Graphs for select FR-β staining intensity and various pathological data (error bars represent SEM) are shown. Lymph node involvement was based upon the AJCC/UICC stage - TxNxMx. Additional graphs and data can be found in the Supporting Information.
Thymoma Tissue Microarray, supplied by Purdue University Cytometry, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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IHC was performed on a BioMax multi-cancer tissue microarray using the FR-β specific monoclonal antibody m909. The relative staining intensity, graded on a scale of 0 to 3, of positively staining cells within the tumor and stroma were determined. A ) Statistically significant differences ( p -value <0.05) using ANOVA or a t-test and correlations using a Spearman correlation ( p -value <0.05) between the average FR-β staining intensity and various pathological data are summarized. B ) Graphs for select FR-β staining intensity and various pathological data (error bars represent SEM) are shown. Lymph node involvement was based upon the AJCC/UICC stage - TxNxMx. Additional graphs and data can be found in the Supporting Information.

Journal: Oncotarget

Article Title: Assessment of folate receptor-β expression in human neoplastic tissues

doi:

Figure Lengend Snippet: IHC was performed on a BioMax multi-cancer tissue microarray using the FR-β specific monoclonal antibody m909. The relative staining intensity, graded on a scale of 0 to 3, of positively staining cells within the tumor and stroma were determined. A ) Statistically significant differences ( p -value <0.05) using ANOVA or a t-test and correlations using a Spearman correlation ( p -value <0.05) between the average FR-β staining intensity and various pathological data are summarized. B ) Graphs for select FR-β staining intensity and various pathological data (error bars represent SEM) are shown. Lymph node involvement was based upon the AJCC/UICC stage - TxNxMx. Additional graphs and data can be found in the Supporting Information.

Article Snippet: The cancer tissue microarrays that were examined in this study were: i) a hepatocellular carcinoma tissue microarray from Emory University (Atlanta, GA), ii) a thymoma tissue microarray from Indiana University-Purdue University Indianapolis (Indianapolis, IN), iii) a custom multi-tumor tissue microarray (TMA-00300) from Asterand (Detroit, MI), iv) a high density multiple organ tumor and normal tissue microarray (MC5003) from US Biomax (Rockville, MD), and v) a breast tumor microarray (ARY-HH0056), a brain glioma tumor microarray (ARY-HH0138) and an endometrial carcinoma progression tumor microarray (ARY-HH0211) from Folio Biosciences (Columbus, OH).

Techniques: Microarray, Staining

IHC was performed on a Asterand tissue microarray using the FR-β specific monoclonal antibody m909. The approximate percentage of positively staining cells within the tumor and stroma were determined. A ) Statistically significant differences ( p -value <0.05) using ANOVA or a t-test and correlations ( p -value <0.05) using a Spearman correlation between the percentage of FR-β staining cells and various pathological data are summarized. B ) Graphs for select FR-β staining and various pathological data (error bars represent SEM) are shown. Lymph node involvement was based upon the AJCC/UICC stage - TxNxMx. Additional graphs and data can be found in the Supporting Information.

Journal: Oncotarget

Article Title: Assessment of folate receptor-β expression in human neoplastic tissues

doi:

Figure Lengend Snippet: IHC was performed on a Asterand tissue microarray using the FR-β specific monoclonal antibody m909. The approximate percentage of positively staining cells within the tumor and stroma were determined. A ) Statistically significant differences ( p -value <0.05) using ANOVA or a t-test and correlations ( p -value <0.05) using a Spearman correlation between the percentage of FR-β staining cells and various pathological data are summarized. B ) Graphs for select FR-β staining and various pathological data (error bars represent SEM) are shown. Lymph node involvement was based upon the AJCC/UICC stage - TxNxMx. Additional graphs and data can be found in the Supporting Information.

Article Snippet: The cancer tissue microarrays that were examined in this study were: i) a hepatocellular carcinoma tissue microarray from Emory University (Atlanta, GA), ii) a thymoma tissue microarray from Indiana University-Purdue University Indianapolis (Indianapolis, IN), iii) a custom multi-tumor tissue microarray (TMA-00300) from Asterand (Detroit, MI), iv) a high density multiple organ tumor and normal tissue microarray (MC5003) from US Biomax (Rockville, MD), and v) a breast tumor microarray (ARY-HH0056), a brain glioma tumor microarray (ARY-HH0138) and an endometrial carcinoma progression tumor microarray (ARY-HH0211) from Folio Biosciences (Columbus, OH).

Techniques: Microarray, Staining