TissueScan, Breast Cancer cDNA Array III

SKU
BCRT103
48 samples covering 12-Stage I, 6-IIA, 10-IIB, 7-IIIA, 3-IIIB, 5-IIIC, 5-IV. Available in 2, 5, 10 identical plates.
New! ER, PR and HER2 in Clinical Info.
  $1,060.00
2 Weeks*
Specifications
Specifications
Product Data
TissueScan Type Cancer Specific
Array Name Breast Cancer cDNA Array III
Clinical Info
Diagnosis Category Breast Cancer
Tissue Breast
Shipping Ambient
Description 48 samples covering 12-Stage I, 6-IIA, 10-IIB, 7-IIIA, 3-IIIB, 5-IIIC, 5-IV. Available in 2, 5, 10 identical plates.
New! ER, PR and HER2 in Clinical Info.
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Integrative analysis of mRNA stability regulation uncovers a metastasis-suppressive program in breast cancer
Karner, Mittmann, Chen et al
Sci Adv (2026) 12 (11), eaea9061-eaea9061 DOI: 10.1126/sciadv.aea9061
Cited by 1
AI Summary: OriGene’s breast cancer cDNA tissue panels (BCRT102, BCRT103) were used to measure TXNIP expression by qPCR across clinical breast cancer samples, enabling analysis of mRNA stability regulation in the study.
Snippet: >TXNIP expression using qPCR in 96 clinical samples across all stages of breast cancer, namely 5 normal epithelial, 23 stage I, 30 stage II, 29 stage III, and 9 stage IV metastatic biopsies (Origene, BCRT102, BCRT103), from which 90 samples yielded sufficient amount of cDNA. HPRT1 was used as an endogenous control and relative TXNIP expression levels were mea
FigureFigureFigure
Integrative analysis of mRNA stability regulation uncovers a metastasis-suppressive program in breast cancer
Karner, Mittmann, Chen et al
bioRxiv (2025)
Cited by 1
AI Summary: OriGene’s breast cancer cDNA panels (BCRT102, BCRT103) were used to measure TXNIP expression by qPCR across clinical samples, enabling the study to assess mRNA stability regulation in breast cancer progression.
Snippet: measured TXNIP expression using qPCR in 96 clinical samples across all stages of breast cancer, namely 5 normal epithelial, 23 stage I, 30 stage II, 29 stage III, and 9 stage IV metastatic biopsies (Origene, BCRT102, BCRT103), from which 90 samples yielded sufficient amount of cDNA. HPRT was used as an endogenous control and relative TXNIP expression levels were measured using the primers listed
FigureFigureFigure
Targeting and Sensitization of Breast Cancer Cells to Killing with a Novel Interleukin-13 Receptor α2-Specific Hybrid Cytolytic Peptide
Jannoo, Walker, Kanamarlapudi
Cancers (2023) 15 (10), 2772 DOI: 10.3390/cancers15102772
Cited by 7
AI Summary: OriGene’s TissueScan™ Breast Cancer cDNA Arrays (CSRT104, BCRT103, and BCRT104) were used in this study to assess IL-13Rα2 mRNA expression across various stages of breast cancer and non-malignant tissues, enabling the evaluation of IL-13Rα2 as a therapeutic target.
Snippet: …For example, IL-13 conjugated with Pseudomonas exotoxin subunits (IL-13;To determine relative IL-13Rα2 mRNA expression in breast cancer tumors representing various stages of the disease, a similar RT-PCR methodology was applied to Origene TissueScan Breast Cancer cDNA Arrays (samples from CSRT104, BCRT103, and BCRT104;60 tumor samples (n = 60) covering various disease stages with non-malignant (n = 7) breast tissue cDNA samples for comparison) [37]
A sense-antisense RNA interaction promotes breast cancer metastasis via regulation of NQO1 expression
Culbertson, Garcia, Markett et al
Nat Cancer (2023) 4 (5), 682-698 DOI: 10.1038/s43018-023-00554-7
Cited by 44
AI Summary: In this study, OriGene products—specifically, the NQO1 shRNA (OriGene, #TF314766) and NQO1-AS shRNA (OriGene, #TL315735)—were used to knock down NQO1 and NQO1-AS expression, enabling the authors to demonstrate that these RNAs promote breast cancer metastasis by regulating NQO1 levels.
Snippet: of this family impact gene expression through different mechanisms, including DNA methylation13, chromatin modification14 and RNA degradation15. Some antisense RNAs have also been associated with tumorigenesis and a select few have a functional role in cancer progression16. Still, the extent to which antisense RNAs contribute to the regulation of gene expression in cancer is poorly understood. G;...
FigureFigureFigure
Targeting prooxidant MnSOD effect inhibits triple-negative breast cancer (TNBC) progression and M2 macrophage functions under the oncogenic stress
Al Haq, Tseng, Chen et al
Cell Death Dis (2022) 13 (1), 49 DOI: 10.1038/s41419-021-04486-x
Cited by 51
AI Summary: OriGene’s breast cancer cDNA arrays were used to analyze and demonstrate elevated SOD2 mRNA expression in advanced-stage breast tumor tissues, supporting the study’s findings on MnSOD’s role in TNBC progression.
Snippet: at MCTS1 and SOD2 expression was positively correlated in breast cancer patients (p ;- Further characterization of SOD2 mRNA levels was conducted with breast cancer cDNA arrays (OriGene). SOD2 expression was enriched among stage II (3.57-fold) and advanced-stage (III/IV) (7.36-fold) tumor tissues (Fig. 1D) relative to normal breast tissues.
FigureFigureFigure
INPP4B promotes PI3Kα-dependent late endosome formation and Wnt/β-catenin signaling in breast cancer
Rodgers, Ooms, Oorschot et al
Nat Commun (2021) 12 (1), 3140 DOI: 10.1038/s41467-021-23241-6
Cited by 66
AI Summary: OriGene’s Tissue Scan Breast Cancer cDNA arrays I-IV (BCRT101, BCRT102, BCRT103, and BCRT104) were used to measure INPP4B mRNA expression in primary human breast cancer and normal tissues, contributing essential data for the study's analysis of INPP4B expression patterns.
Snippet: 1b, c). As mRNA expression data were not available for these cohorts, INPP4B mRNA expression was examined using Tissue Scan Breast Cancer cDNA arrays I-IV (OriGene) of 130 primary human breast cancers and 16 normal breast tissues (Fig. 1c);Breast cancer cDNA arrays (176 breast cancers and 16 tumor adjacent normal breast tissues) were purchased from OriGene (BCRT101, BCRT102, BCRT103, and BCRT104)
Showing 1-6 of 20 papers.
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