sybr-green-i and Adenocarcinoma

sybr-green-i has been researched along with Adenocarcinoma* in 3 studies

Other Studies

3 other study(ies) available for sybr-green-i and Adenocarcinoma

ArticleYear
Development of a SYBR Green-based real-time quantitative polymerase chain reaction assay to detect enzootic nasal tumor virus in goats.
    Canadian journal of veterinary research = Revue canadienne de recherche veterinaire, 2021, Volume: 85, Issue:2

    Topics: Adenocarcinoma; Animals; Benzothiazoles; Betaretrovirus; Diamines; Goat Diseases; Goats; Nose Neoplasms; Quinolines; Real-Time Polymerase Chain Reaction; Retroviridae Infections; Tumor Virus Infections

2021
Application of a modified real-time PCR technique for relative gene copy number quantification to the determination of the relationship between NKX3.1 loss and MYC gain in prostate cancer.
    Clinical chemistry, 2005, Volume: 51, Issue:3

    Topics: Adenocarcinoma; Benzothiazoles; Cell Line, Tumor; Diamines; Female; Fluorescent Dyes; Gene Dosage; Genes, myc; Homeodomain Proteins; Humans; Male; Organic Chemicals; Polymerase Chain Reaction; Prostatic Neoplasms; Quinolines; Reference Values; Transcription Factors

2005
Quantitative determination of tumor cell intravasation in a real-time polymerase chain reaction-based assay.
    Clinical & experimental metastasis, 2002, Volume: 19, Issue:4

    Tumor cells acquire the ability to enter blood vessels surrounding the primary tumor, endowing them with the capacity to disseminate and become established in distant sites, originating a metastasis. Determination of the intravasation ability of tumor cells is thus important, as it can be correlated with their potential malignancy. To analyze the intravasation phenotype of human tumor cells in vivo, we performed chick embryo chorioallantoic membrane (CAM) assays. Cells were inoculated on the CAM of 9-day-old chick embryos and the membrane at the opposite side of the egg was recovered after 48 h incubation. To measure intravasation ability, we calculated the amount of human DNA in each CAM sample by real-time PCR of Alu sequences and SYBR Green 1 fluorescence detection. This analysis showed a detection limit of 1 human cell per 10(5) total cells, and we were able to distinguish between tumor cells of distinct invasive capacity. This assay has several advantages over current methods to measure intravasation ability, including the elimination of post-PCR analysis, sensitivity and easy scale-up of sample numbers.

    Topics: Adenocarcinoma; Allantois; Alu Elements; Animals; Benzothiazoles; Breast Neoplasms; Chick Embryo; Chorion; Computer Systems; Diamines; DNA, Neoplasm; Ethidium; Fibroblasts; Fluorescent Dyes; Humans; Neoplasm Invasiveness; Organic Chemicals; Phenotype; Polymerase Chain Reaction; Quinolines; Tumor Cells, Cultured; Urinary Bladder Neoplasms

2002