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cdnas  (OriGene)


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    Structured Review

    OriGene cdnas
    Cdnas, supplied by OriGene, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tissuescan+ovarian+cancer+cdna+arrays/TissueScan%2C+Ovarian+Cancer+cDNA+Array+II/10__1158_slash_1535___7163__mct___23___0550-85-32-42
    Average 92 stars, based on 4 article reviews
    cdnas - by Bioz Stars, 2026-10
    92/100 stars

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    Related Articles

    Expressing:

    Article Title: EFA6R suppresses ovarian cancer cell migration and invasion
    Article Snippet: .. EFA6R gene (mRNA) expression was carried out in healthy and cancer ovarian tissues by RT-qPCR using TissuescanTM ovarian cancer cDNA arrays I-IV (Origene Technologies, USA) and EFA6R (NM_206909.3) sequence-specific primers (Forward 5’-CGCAGCGGCAGAGACATTT-3’ and Reverse 5’-TTTGGCCTTGGCAACACTCT-3’); the cDNA arrays were pre-normalised to β-actin expression. .. For cell lines, total RNA was extracted from cell lines using TRI Reagent ( Sigma, UK ) . cDNA was prepared from total RNA using the High Capacity cDNA Reverse Transcription Kit (Thermo Fisher Scientific, UK) ( ).

    Article Title: Hedgehog/GLI1 Transcriptionally Regulates FANCD2 in Ovarian Tumor Cells: Its Inhibition Induces HR-Deficiency and Synergistic Lethality with PARP Inhibition.
    Article Snippet: Prism 7 (GraphPad Prism) was used to perform t-test and to calculate statistical significance. .. Ovarian Cancer cDNA Array IV Kit (Cat No: HORT104, Origene) was used to study the expression levels of FANCD2 and GLI1 in the different stages of OC according to the manufacturer's protocol. ..

    Article Title: Matriptase drives dissemination of ovarian cancer spheroids by a PAR-2/PI3K/Akt/MMP9 signaling axis.
    Article Snippet: The transmembrane serine protease matriptase is a key regulator of both barrier-disruptive and protective epithelial cell–cell interactions.. Elevated matriptase is a consistent feature of epithelial ovarian cancers (OvCa), where multicellular spheroids shed from the primary tumor into the peritoneal cavity are critical drivers of metastasis.. Dynamic cell-to-cell adhesive contacts are required for spheroid formation and maintenance.

    Quantitative RT-PCR:

    Article Title: EFA6R suppresses ovarian cancer cell migration and invasion
    Article Snippet: .. EFA6R gene (mRNA) expression was carried out in healthy and cancer ovarian tissues by RT-qPCR using TissuescanTM ovarian cancer cDNA arrays I-IV (Origene Technologies, USA) and EFA6R (NM_206909.3) sequence-specific primers (Forward 5’-CGCAGCGGCAGAGACATTT-3’ and Reverse 5’-TTTGGCCTTGGCAACACTCT-3’); the cDNA arrays were pre-normalised to β-actin expression. .. For cell lines, total RNA was extracted from cell lines using TRI Reagent ( Sigma, UK ) . cDNA was prepared from total RNA using the High Capacity cDNA Reverse Transcription Kit (Thermo Fisher Scientific, UK) ( ).

    Sequencing:

    Article Title: EFA6R suppresses ovarian cancer cell migration and invasion
    Article Snippet: .. EFA6R gene (mRNA) expression was carried out in healthy and cancer ovarian tissues by RT-qPCR using TissuescanTM ovarian cancer cDNA arrays I-IV (Origene Technologies, USA) and EFA6R (NM_206909.3) sequence-specific primers (Forward 5’-CGCAGCGGCAGAGACATTT-3’ and Reverse 5’-TTTGGCCTTGGCAACACTCT-3’); the cDNA arrays were pre-normalised to β-actin expression. .. For cell lines, total RNA was extracted from cell lines using TRI Reagent ( Sigma, UK ) . cDNA was prepared from total RNA using the High Capacity cDNA Reverse Transcription Kit (Thermo Fisher Scientific, UK) ( ).

    Gene Expression:

    Article Title: PRSS21/Testisin inhibits ovarian tumor metastasis and antagonizes proangiogenic angiopoietins ANG2 and ANGPTL4
    Article Snippet: The Human Angiogenesis TaqMan array (ThermoFisher), containing 92 genes associated with vascular function, was probed by qPCR using RNA isolated from ES-2-Luc-TsWT and ES-2-Luc-Ctl cell lines. mRNA expression was normalized to GAPDH. .. The TissueScan Ovarian Cancer cDNA Array II (II (HORT502; Origene) containing 48 samples covering four disease stages of varying histopathologies, and normal tissues was screened for testisin and PAR-2 mRNA gene expression using TaqMan Master Mix and the primers listed above. .. Cell lines and tumor tissues were lysed in cell lysis buffer (0.5% Triton X-100, 0.5% NP40, 60mM HEPES (pH 7.3), 150 mM NaCl, Complete Mini Protease Inhibitor Cocktail & PhosSTOP Phosphatase Inhibitor Cocktail (Roche, Indianapolis, IN)).

    Article Title: The Peptide-Drug Conjugate TH1902: A New Sortilin Receptor-Mediated Cancer Therapeutic against Ovarian and Endometrial Cancers
    Article Snippet: .. SORT1 gene expression in a TissueScan ovarian cancer cDNA array II (OriGene, #HORT102, Rockville, MD, USA) was quantified by qPCR using SsoFast EvaGreen ® Supermix (Bio-Rad) in a CFX Connect Real-Time PCR System (Bio-Rad, Mississauga, ON, Canada). ..

    Article Title: Selective targeting of metastatic ovarian cancer using an engineered anthrax prodrug activated by membrane-anchored serine proteases
    Article Snippet: RT-qPCR was performed using primers for human testisin (Hs00199035_m1), hepsin (Hs01056332_m1), matriptase (Hs00222707_m1), HAI-1 (Hs00173678_m1), HAI-2 (Hs01070442_m1), ANTXR1 (Hs00216777_m1), ANTXR2 (Hs00292467_m1), GAPDH (Hs02758991_g1) and -actin (Hs99999903_m1). .. The TissueScan Ovarian Cancer cDNA Array II (Origene) (HORT102) containing 40 samples covering four disease stages (8 stage I, 9 stage II, 17 stage III, and 6 stage IV) of varying OvCa histopathologies, and 8 normal tissues, was screened for hepsin, testisin and matriptase mRNA gene expression using the primers listed above. ..

    Real-time Polymerase Chain Reaction:

    Article Title: The Peptide-Drug Conjugate TH1902: A New Sortilin Receptor-Mediated Cancer Therapeutic against Ovarian and Endometrial Cancers
    Article Snippet: .. SORT1 gene expression in a TissueScan ovarian cancer cDNA array II (OriGene, #HORT102, Rockville, MD, USA) was quantified by qPCR using SsoFast EvaGreen ® Supermix (Bio-Rad) in a CFX Connect Real-Time PCR System (Bio-Rad, Mississauga, ON, Canada). ..

    other:

    Article Title: Expression of DNA Methyltransferase 3B Isoforms Is Associated with DNA Satellite 2 Hypomethylation and Clinical Prognosis in Advanced High-Grade Serous Ovarian Carcinoma
    Article Snippet: To validate that DNMT3B3 is overexpressed in advanced stages of HGSOC, we used two arrays of cDNA rapid cDNA panels: II and III, of ovarian carcinoma (TissueScan Ovarian Cancer cDNA arrays II and III) (OriGene Technologies, Rockville, MD, USA) (cat. no. HORT102 and 103), and both had 14 ovaries without cancer and 82 ovarian carcinoma samples of cDNA to be analyzed ( ).



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    OriGene tumorigenic development
    Fig. 6. Potent antitumor cytotoxicity of PAS:LF toxin in patient-derived primary human tumors. (A) Real-time qPCR analysis showing increased hepsin, testisin, and matriptase mRNA expression in patients with OvCa of various histological type and stage of <t>tumorigenic</t> development (Human Ovarian Cancer TissueScan Array; Origene) compared with normal ovary tissue. Data are representedin box plots showing the median, lower and upper quartiles (horizontal lines) of rela- tive expression +SEM compared to normal ovary tissue normalized to β-actin (*P < 0.05, ***P < 0.005, ****P < 0.001). (B) Tumor cells recovered from ascites fluids from five patients were collected by centrifugation, contaminating red blood cells were removed by hypotonic lysis, and cytospins were assessed for tumor purity by Kwik-Diff stain and expression of the OvCa markers CA125 and PAX8. Images are 40X original magnification. Insets are close-up images of indi- vidual cells or clusters. The tumor cell percentage of total cells in ascites fluid was quantified using ImageJ. The chemotherapy (Chemo) treatment status, histo- logical subtype, tumor stage, and primary tumor origin were determined by independent staff pathologists as part of the clinical diagnosis. HGSOC, high-grade serous ovarian carcinoma; LGSOC, low-grade serous ovarian carcinoma. (C) (i) The recovered human ascites tumor cells were seeded on agarose-coated plates for 24 h, where they formed organotypic multicellular spheroids. Spheroids that were treated twice with PAS:LF (Patients #1 and #2: 2 μg/mL, Patients #3 to #5: 6 μg/mL) for a total of 120 h. Spheroid viability relative to untreated controls was quantified via PrestoBlue or ImageJ quantification of decrease in size and is shown as an average of the five patient samples ± SEM performed in three to six replicates (****P < 0.001; ns, not significant). (ii) Representative images of spheroids from Patient #4 and Patient #5 after 120 h of treatment are shown. Scale bars = 650μm.
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    Image Search Results


    DNMT3B3 overexpression validated in advanced stages of high-grade serous ovarian carcinoma (HGSOC). DNMT3B3 isoform overexpression in two arrays of cDNA rapid cDNA panels: II and III, of ovarian carcinoma (TissueScan Ovarian Cancer cDNA arrays II and III) (OriGene Technologies, Rockville MD) (cat. no. HORT102, and 103) (n = 82). Non-advanced HGSOC (n = 23: mucinous, low-grade serous ovarian carcinoma, endometrioid, carcinoma clear cells, and stages I–II of HGSOC) versus advanced HGSOC (n = 59: stages III–IV of HGSOC). Assays were normalized with GAPDH expression in each case and ten controls of the normal ovary. Mann–Whitney U test was used.

    Journal: International Journal of Molecular Sciences

    Article Title: Expression of DNA Methyltransferase 3B Isoforms Is Associated with DNA Satellite 2 Hypomethylation and Clinical Prognosis in Advanced High-Grade Serous Ovarian Carcinoma

    doi: 10.3390/ijms232112759

    Figure Lengend Snippet: DNMT3B3 overexpression validated in advanced stages of high-grade serous ovarian carcinoma (HGSOC). DNMT3B3 isoform overexpression in two arrays of cDNA rapid cDNA panels: II and III, of ovarian carcinoma (TissueScan Ovarian Cancer cDNA arrays II and III) (OriGene Technologies, Rockville MD) (cat. no. HORT102, and 103) (n = 82). Non-advanced HGSOC (n = 23: mucinous, low-grade serous ovarian carcinoma, endometrioid, carcinoma clear cells, and stages I–II of HGSOC) versus advanced HGSOC (n = 59: stages III–IV of HGSOC). Assays were normalized with GAPDH expression in each case and ten controls of the normal ovary. Mann–Whitney U test was used.

    Article Snippet: Testing was carried out in two arrays of rapid cDNA panels: II and III, of ovarian carcinoma (TissueScan Ovarian Cancer cDNA arrays II and III) (OriGene Technologies, Rockville, MD, USA) (cat. no. HORT102 and 103) (n = 82).

    Techniques: Over Expression, Expressing, MANN-WHITNEY

    Fig. 6. Potent antitumor cytotoxicity of PAS:LF toxin in patient-derived primary human tumors. (A) Real-time qPCR analysis showing increased hepsin, testisin, and matriptase mRNA expression in patients with OvCa of various histological type and stage of tumorigenic development (Human Ovarian Cancer TissueScan Array; Origene) compared with normal ovary tissue. Data are representedin box plots showing the median, lower and upper quartiles (horizontal lines) of rela- tive expression +SEM compared to normal ovary tissue normalized to β-actin (*P < 0.05, ***P < 0.005, ****P < 0.001). (B) Tumor cells recovered from ascites fluids from five patients were collected by centrifugation, contaminating red blood cells were removed by hypotonic lysis, and cytospins were assessed for tumor purity by Kwik-Diff stain and expression of the OvCa markers CA125 and PAX8. Images are 40X original magnification. Insets are close-up images of indi- vidual cells or clusters. The tumor cell percentage of total cells in ascites fluid was quantified using ImageJ. The chemotherapy (Chemo) treatment status, histo- logical subtype, tumor stage, and primary tumor origin were determined by independent staff pathologists as part of the clinical diagnosis. HGSOC, high-grade serous ovarian carcinoma; LGSOC, low-grade serous ovarian carcinoma. (C) (i) The recovered human ascites tumor cells were seeded on agarose-coated plates for 24 h, where they formed organotypic multicellular spheroids. Spheroids that were treated twice with PAS:LF (Patients #1 and #2: 2 μg/mL, Patients #3 to #5: 6 μg/mL) for a total of 120 h. Spheroid viability relative to untreated controls was quantified via PrestoBlue or ImageJ quantification of decrease in size and is shown as an average of the five patient samples ± SEM performed in three to six replicates (****P < 0.001; ns, not significant). (ii) Representative images of spheroids from Patient #4 and Patient #5 after 120 h of treatment are shown. Scale bars = 650μm.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Selective targeting of metastatic ovarian cancer using an engineered anthrax prodrug activated by membrane-anchored serine proteases.

    doi: 10.1073/pnas.2201423119

    Figure Lengend Snippet: Fig. 6. Potent antitumor cytotoxicity of PAS:LF toxin in patient-derived primary human tumors. (A) Real-time qPCR analysis showing increased hepsin, testisin, and matriptase mRNA expression in patients with OvCa of various histological type and stage of tumorigenic development (Human Ovarian Cancer TissueScan Array; Origene) compared with normal ovary tissue. Data are representedin box plots showing the median, lower and upper quartiles (horizontal lines) of rela- tive expression +SEM compared to normal ovary tissue normalized to β-actin (*P < 0.05, ***P < 0.005, ****P < 0.001). (B) Tumor cells recovered from ascites fluids from five patients were collected by centrifugation, contaminating red blood cells were removed by hypotonic lysis, and cytospins were assessed for tumor purity by Kwik-Diff stain and expression of the OvCa markers CA125 and PAX8. Images are 40X original magnification. Insets are close-up images of indi- vidual cells or clusters. The tumor cell percentage of total cells in ascites fluid was quantified using ImageJ. The chemotherapy (Chemo) treatment status, histo- logical subtype, tumor stage, and primary tumor origin were determined by independent staff pathologists as part of the clinical diagnosis. HGSOC, high-grade serous ovarian carcinoma; LGSOC, low-grade serous ovarian carcinoma. (C) (i) The recovered human ascites tumor cells were seeded on agarose-coated plates for 24 h, where they formed organotypic multicellular spheroids. Spheroids that were treated twice with PAS:LF (Patients #1 and #2: 2 μg/mL, Patients #3 to #5: 6 μg/mL) for a total of 120 h. Spheroid viability relative to untreated controls was quantified via PrestoBlue or ImageJ quantification of decrease in size and is shown as an average of the five patient samples ± SEM performed in three to six replicates (****P < 0.001; ns, not significant). (ii) Representative images of spheroids from Patient #4 and Patient #5 after 120 h of treatment are shown. Scale bars = 650μm.

    Article Snippet: Potent antitumor cytotoxicity of PAS:LF toxin in patient-derived primary human tumors. (A) Real-time qPCR analysis showing increased hepsin, testisin, and matriptase mRNA expression in patients with OvCa of various histological type and stage of tumorigenic development (Human Ovarian Cancer TissueScan Array; Origene) compared with normal ovary tissue.

    Techniques: Derivative Assay, Expressing, Centrifugation, Lysis, Staining, Biomarker Discovery