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R&D Systems
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ATCC
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OriGene
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Novus Biologicals
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R&D Systems
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R&D Systems
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Immunex Corporation
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Santa Cruz Biotechnology
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Santa Cruz Biotechnology
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Bio-Rad
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Immunex Corporation
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Image Search Results
Journal: Endocrine-Related Cancer
Article Title: GATA4 protects granulosa cell tumors from TRAIL-induced apoptosis
doi: 10.1677/erc-10-0041
Figure Lengend Snippet: Figure 1 Immunohistochemical analysis of death receptors DR4 (A, C, and E) and DR5 (B, D, and F) from tissue microarray of GCTs. Examples of strong, intermediate, and low expression are depicted in upper, middle, and lower rows respectively. Higher magnifications are shown in insets. Brown color indicates positive staining. Scale bar is 50 mm.
Article Snippet: Primary antibodies were as follows: mouse antihuman a-inhibin IgG (MCA 9515, AbD Serotec, Oxford, UK) at dilution of 1:100, goat antihuman antiMüllerian hormone (AMH) IgG (sc-6886, Santa Cruz Biotechnology, Inc.) at dilution of 1:100, and goat antihuman GATA4 IgG (sc-1237, Santa Cruz Biotechnology) at dilution of 1:200;
Techniques: Immunohistochemical staining, Microarray, Expressing, Staining
Journal: Endocrine-Related Cancer
Article Title: GATA4 protects granulosa cell tumors from TRAIL-induced apoptosis
doi: 10.1677/erc-10-0041
Figure Lengend Snippet: Figure 2 Immunohistochemical analysis of TRAIL receptors DR4 (A), DR5 (B), and GCT markers AMH (C), a-inhibin (inh-a) (D), and GATA4 (E) in cultured GCT cells. Brown color indicates positive staining. (F) A negative control using secondary antibody only. Higher magnifications are shown in insets. Scale bar is 50 mm.
Article Snippet: Primary antibodies were as follows: mouse antihuman a-inhibin IgG (MCA 9515, AbD Serotec, Oxford, UK) at dilution of 1:100, goat antihuman antiMüllerian hormone (AMH) IgG (sc-6886, Santa Cruz Biotechnology, Inc.) at dilution of 1:100, and goat antihuman GATA4 IgG (sc-1237, Santa Cruz Biotechnology) at dilution of 1:200;
Techniques: Immunohistochemical staining, Cell Culture, Staining, Negative Control
Journal: The Journal of investigative dermatology
Article Title: Blockade of death receptor-mediated pathways early in the signaling cascade coincides with distinct apoptosis resistance in cutaneous T-cell lymphoma cells.
doi: 10.1038/sj.jid.5700868
Figure Lengend Snippet: Figure 3. High expression of CD95 and TRAIL receptors in CTCL cells. Surface expression of death receptors (DR4, DR5, and CD95) was determined by flow cytometry for the CTCL and T-ALL cell lines. The cells were stained with (a) specific monoclonal TRAIL-R1/DR4, (b) TRAIL-R2/DR5, and (c) CD95-specific antibody (filled graphs). Isotype control antibodies were used as negative controls (open graphs). A shift to the right indicates increased surface expression. (d) Median expression values obtained for the individual cell lines (each two independent experiments) were normalized with respect to the mean expression in all eight cell lines. (+) indicates the loss of CD95 expression in SeAx.
Article Snippet: The following antibodies were used:
Techniques: Expressing, Flow Cytometry, Staining, Control
Journal: The Journal of investigative dermatology
Article Title: Blockade of death receptor-mediated pathways early in the signaling cascade coincides with distinct apoptosis resistance in cutaneous T-cell lymphoma cells.
doi: 10.1038/sj.jid.5700868
Figure Lengend Snippet: Figure 5. Weak expression of TNF-R1, caspase-10, and Bid in CTCL cell lines. Western blot analysis for (a) DR4, DR5, and TNF-R1, (b) for procaspase-3, -8, and -10 as well as for (c) FADD, Bid, and caspase-9 are shown for CTCL cell lines (HH, HuT-78, MyLa, SeAx) and for T-ALL cell lines (Jurkat, CCRF-CEM, MOLT-4, Karpas-45). Molecular weights are indicated as 44 (DR4), 47/40 (DR5), 55 (TNF-R1), 30 (caspase-3), 55/53 (caspase-8), 60/55 (caspase-10), 25 (FADD), 18 (Bid), 45 (caspase-9), 50 (a-tubulin), and 37 kDa (glyceraldehyde-3-phosphate dehydrogenase). Identical protein amounts (25 mg per lane) had been loaded to each lane. Consistent blotting was confirmed by Ponceau red staining and evaluation of a-tubulin or GAPDH expression. Expression of Bid in MyLa cells was not detectable here as short exposure times were used for chemiluminescence detection to avoid signal saturation in other cell lines. However, weak expression of Bid can be seen in MyLa after longer exposure, as shown in Figure 2, whereas HH remained negative. Two experiments performed for each cell line starting from independent cultures revealed reproducible results.
Article Snippet: The following antibodies were used:
Techniques: Expressing, Western Blot, Staining
Journal: Cancers
Article Title: Targeting of CD133+ Cancer Stem Cells by Mesenchymal Stem Cell Expressing TRAIL Reveals a Prospective Role of Apoptotic Gene Regulation in Non-Small Cell Lung Cancer
doi: 10.3390/cancers11091261
Figure Lengend Snippet: TRAIL sensitivity by in vitro characterization. ( A ) The half maximal inhibitory concentration (IC 50 ) value was determined in non-small cell lung cancer (NSCLC) cell lines (H460, H2170 and A549) by MTS assay after 48 h of rhTRAIL treatment at different concentrations. ( B ) Analysis of TRAIL receptors expression [agonist receptors (DR4 and DR5) and decoy receptors (DcR1 and DcR2)] in MSCs and NSCLC cell lines by flow cytometry. ( C ) Sensitivity of NSCLC cell lines and MSCs evaluated by MTS assay after rhTRAIL (500 ng/mL) treatment.
Article Snippet: The NSCLC cell lines were analyzed for TRAIL agonist (DR4 and DR5) and other decoy receptors (DcR1 and DcR2) with
Techniques: In Vitro, Concentration Assay, MTS Assay, Expressing, Flow Cytometry
Journal: Cancers
Article Title: Targeting of CD133+ Cancer Stem Cells by Mesenchymal Stem Cell Expressing TRAIL Reveals a Prospective Role of Apoptotic Gene Regulation in Non-Small Cell Lung Cancer
doi: 10.3390/cancers11091261
Figure Lengend Snippet: Flow cytometry analysis of CD133+ NSCLC-derived cancer stem cells (CSCs) and their TRAIL receptor expression. ( A ) Cell debris and doublets were discriminated, and dead cells were excluded [(DAPI/4′,6-diamidino-2-phenylindole) negative; shown by the first four panels], followed by isolation of the CD133+ population in NSCLC cell lines (A549, H2170, and H460) in the lower panels. ( B ) Both CD133+ CSCs of H2170 and H460 expressed a high level of TRAIL cognate receptor (DR5), consistent with their sensitivity to TRAIL.
Article Snippet: The NSCLC cell lines were analyzed for TRAIL agonist (DR4 and DR5) and other decoy receptors (DcR1 and DcR2) with
Techniques: Flow Cytometry, Derivative Assay, Expressing, Isolation