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Lonza primary prostatic epithelial prec cells
Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary <t>epithelial</t> cell line <t>PrEC</t> (C) was detected by RT-PCR. β-Actin expression was used as a loading control.
Primary Prostatic Epithelial Prec Cells, supplied by Lonza, 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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Rockland Immunochemicals normal human prostate epithelial cell rna (prec)
Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary <t>epithelial</t> cell line <t>PrEC</t> (C) was detected by RT-PCR. β-Actin expression was used as a loading control.
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Lonza prec normal human prostate epithelial cells
Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary <t>epithelial</t> cell line <t>PrEC</t> (C) was detected by RT-PCR. β-Actin expression was used as a loading control.
Prec Normal Human Prostate Epithelial Cells, supplied by Lonza, 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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Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary <t>epithelial</t> cell line <t>PrEC</t> (C) was detected by RT-PCR. β-Actin expression was used as a loading control.
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Biowhittaker Inc normal human prostate epithelial cells (prec)
Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary <t>epithelial</t> cell line <t>PrEC</t> (C) was detected by RT-PCR. β-Actin expression was used as a loading control.
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Lonza clonetics® normal human prostate epithelial cells (prec)
Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary <t>epithelial</t> cell line <t>PrEC</t> (C) was detected by RT-PCR. β-Actin expression was used as a loading control.
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Lonza normal human prostate epithelial cells' lines prec-cloneticstm
Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary <t>epithelial</t> cell line <t>PrEC</t> (C) was detected by RT-PCR. β-Actin expression was used as a loading control.
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Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary epithelial cell line PrEC (C) was detected by RT-PCR. β-Actin expression was used as a loading control.

Journal: Journal of Virology

Article Title: Evaluation of Cellular Determinants Required for In Vitro Xenotropic Murine Leukemia Virus-Related Virus Entry into Human Prostate Cancer and Noncancerous Cells

doi: 10.1128/JVI.00274-10

Figure Lengend Snippet: Differential expression of XPR1 gene in immortalized cell lines. Xpr1 expression in prostate cancer (A), immortalized prostate cell lines (B), and the primary epithelial cell line PrEC (C) was detected by RT-PCR. β-Actin expression was used as a loading control.

Article Snippet: In addition, we also used nonimmortalized fibroblast cell lines, Pt-N and Pt-C, which were derived from benign and malignant prostate tissues, respectively ( 39 ), and the established primary prostatic epithelial PrEC cells (Lonza).

Techniques: Quantitative Proteomics, Expressing, Reverse Transcription Polymerase Chain Reaction, Control

XMRV pseudovirus infectivity in prostate cancer cell lines (A), immortalized prostate fibroblast cell lines (B), epithelial cell lines with or without Xpr1 transfection (C), smooth muscle cell lines (D) with or without Xpr1 transfection, and primary epithelial cells (PrEC) (E). Representative images in the fluorescence and bright fields were captured at ×20 magnification. The experiments were carried out twice, and each time the experiments were performed in triplicate. (F) The average levels of GFP expression in infected cells were quantified by FACS analysis. Xpr1 expression levels were determined by quantitative real-time RT-PCR (G) and Western blotting (H). Asterisks indicate statistical significance (P < 0.001).

Journal: Journal of Virology

Article Title: Evaluation of Cellular Determinants Required for In Vitro Xenotropic Murine Leukemia Virus-Related Virus Entry into Human Prostate Cancer and Noncancerous Cells

doi: 10.1128/JVI.00274-10

Figure Lengend Snippet: XMRV pseudovirus infectivity in prostate cancer cell lines (A), immortalized prostate fibroblast cell lines (B), epithelial cell lines with or without Xpr1 transfection (C), smooth muscle cell lines (D) with or without Xpr1 transfection, and primary epithelial cells (PrEC) (E). Representative images in the fluorescence and bright fields were captured at ×20 magnification. The experiments were carried out twice, and each time the experiments were performed in triplicate. (F) The average levels of GFP expression in infected cells were quantified by FACS analysis. Xpr1 expression levels were determined by quantitative real-time RT-PCR (G) and Western blotting (H). Asterisks indicate statistical significance (P < 0.001).

Article Snippet: In addition, we also used nonimmortalized fibroblast cell lines, Pt-N and Pt-C, which were derived from benign and malignant prostate tissues, respectively ( 39 ), and the established primary prostatic epithelial PrEC cells (Lonza).

Techniques: Infection, Transfection, Fluorescence, Expressing, Quantitative RT-PCR, Western Blot