dual-laser dna microarray scanner Search Results


99
Agilent technologies dual laser microarray scanner
Figure 2. Expression values of four CRT-responsive genes evaluated by <t>microarray</t> in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.
Dual Laser Microarray Scanner, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
Danaher Inc microarray dual channel laser scanner
Figure 2. Expression values of four CRT-responsive genes evaluated by <t>microarray</t> in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.
Microarray Dual Channel Laser Scanner, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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CapitalBio Corporation reconstructive luxscantm-10k/a dual-channel laser confocal microarray scanner
Figure 2. Expression values of four CRT-responsive genes evaluated by <t>microarray</t> in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.
Reconstructive Luxscantm 10k/A Dual Channel Laser Confocal Microarray Scanner, supplied by CapitalBio Corporation, 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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CapitalBio Corporation luxscan™-10k/a dual-channel laser confocal microarray scanner
Figure 2. Expression values of four CRT-responsive genes evaluated by <t>microarray</t> in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.
Luxscan™ 10k/A Dual Channel Laser Confocal Microarray Scanner, supplied by CapitalBio Corporation, 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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luxscan™-10k/a dual-channel laser confocal microarray scanner - by Bioz Stars, 2026-07
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CapitalBio Corporation luxscan 10k/a dual-channel laser microarray scanner
Figure 2. Expression values of four CRT-responsive genes evaluated by <t>microarray</t> in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.
Luxscan 10k/A Dual Channel Laser Microarray Scanner, supplied by CapitalBio Corporation, 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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luxscan 10k/a dual-channel laser microarray scanner - by Bioz Stars, 2026-07
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CapitalBio Corporation dual laser scanner luxscan 10k/a
Figure 2. Expression values of four CRT-responsive genes evaluated by <t>microarray</t> in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.
Dual Laser Scanner Luxscan 10k/A, supplied by CapitalBio Corporation, 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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CapitalBio Corporation data were analyzed by scanarray express
Figure 2. Expression values of four CRT-responsive genes evaluated by <t>microarray</t> in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.
Data Were Analyzed By Scanarray Express, supplied by CapitalBio Corporation, 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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data were analyzed by scanarray express - by Bioz Stars, 2026-07
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96
GE Healthcare cy5‑streptavidin
Figure 2. Expression values of four CRT-responsive genes evaluated by <t>microarray</t> in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.
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90
Biozol Diagnostica Vertrieb GmbH cy3-coupled secondary goat anti-mouse antibody
Tissue microarrays of normal tissues and tumors of the respective tissue. First and third lane: normal tissue; second and fourth lane: tumors of the same type of tissue as the normal tissue above. Microarrays containing frozen sections of various tissue samples were purchased from BioCat (Heidelberg, Germany). In brief, the sections were treated with 0.3% H2O2 for 30 min at room temperature (RT). After washing with PBS, the sections were blocked with 10% normal bovine serum for 1 h at RT and subsequently stained with a rabbit anti-human-β2-adrenoceptor antibody (a Santa Cruz Biotechnology, Santa Cruz, CA) and a mouse anti-human neurofilament protein antibody (b Dako Cytomatation, Hamburg, Germany) at 4°C overnight. After washing with PBS, the arrays were incubated with a <t>Cy3-coupled</t> secondary goat anti-rabbit or anti-mouse antibody (Dianova, Hamburg, Germany) for 1 h at RT, and the fluorescence of the samples was analyzed using a dual-laser microarray scanner. In (c), the respective tissue origin is shown
Cy3 Coupled Secondary Goat Anti Mouse Antibody, supplied by Biozol Diagnostica Vertrieb GmbH, 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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Rosetta Biosoftware rosetta resolver gene expression data analysis system
Tissue microarrays of normal tissues and tumors of the respective tissue. First and third lane: normal tissue; second and fourth lane: tumors of the same type of tissue as the normal tissue above. Microarrays containing frozen sections of various tissue samples were purchased from BioCat (Heidelberg, Germany). In brief, the sections were treated with 0.3% H2O2 for 30 min at room temperature (RT). After washing with PBS, the sections were blocked with 10% normal bovine serum for 1 h at RT and subsequently stained with a rabbit anti-human-β2-adrenoceptor antibody (a Santa Cruz Biotechnology, Santa Cruz, CA) and a mouse anti-human neurofilament protein antibody (b Dako Cytomatation, Hamburg, Germany) at 4°C overnight. After washing with PBS, the arrays were incubated with a <t>Cy3-coupled</t> secondary goat anti-rabbit or anti-mouse antibody (Dianova, Hamburg, Germany) for 1 h at RT, and the fluorescence of the samples was analyzed using a dual-laser microarray scanner. In (c), the respective tissue origin is shown
Rosetta Resolver Gene Expression Data Analysis System, supplied by Rosetta Biosoftware, 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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CapitalBio Corporation luxscan 10ka dual pathways laser scanner
Tissue microarrays of normal tissues and tumors of the respective tissue. First and third lane: normal tissue; second and fourth lane: tumors of the same type of tissue as the normal tissue above. Microarrays containing frozen sections of various tissue samples were purchased from BioCat (Heidelberg, Germany). In brief, the sections were treated with 0.3% H2O2 for 30 min at room temperature (RT). After washing with PBS, the sections were blocked with 10% normal bovine serum for 1 h at RT and subsequently stained with a rabbit anti-human-β2-adrenoceptor antibody (a Santa Cruz Biotechnology, Santa Cruz, CA) and a mouse anti-human neurofilament protein antibody (b Dako Cytomatation, Hamburg, Germany) at 4°C overnight. After washing with PBS, the arrays were incubated with a <t>Cy3-coupled</t> secondary goat anti-rabbit or anti-mouse antibody (Dianova, Hamburg, Germany) for 1 h at RT, and the fluorescence of the samples was analyzed using a dual-laser microarray scanner. In (c), the respective tissue origin is shown
Luxscan 10ka Dual Pathways Laser Scanner, supplied by CapitalBio Corporation, 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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90
Lumonics Inc gsi lite dual confocal laser scanner
Tissue microarrays of normal tissues and tumors of the respective tissue. First and third lane: normal tissue; second and fourth lane: tumors of the same type of tissue as the normal tissue above. Microarrays containing frozen sections of various tissue samples were purchased from BioCat (Heidelberg, Germany). In brief, the sections were treated with 0.3% H2O2 for 30 min at room temperature (RT). After washing with PBS, the sections were blocked with 10% normal bovine serum for 1 h at RT and subsequently stained with a rabbit anti-human-β2-adrenoceptor antibody (a Santa Cruz Biotechnology, Santa Cruz, CA) and a mouse anti-human neurofilament protein antibody (b Dako Cytomatation, Hamburg, Germany) at 4°C overnight. After washing with PBS, the arrays were incubated with a <t>Cy3-coupled</t> secondary goat anti-rabbit or anti-mouse antibody (Dianova, Hamburg, Germany) for 1 h at RT, and the fluorescence of the samples was analyzed using a dual-laser microarray scanner. In (c), the respective tissue origin is shown
Gsi Lite Dual Confocal Laser Scanner, supplied by Lumonics Inc, 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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Image Search Results


Figure 2. Expression values of four CRT-responsive genes evaluated by microarray in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.

Journal: Cancer biology & therapy

Article Title: The radiation-induced cell-death signaling pathway is activated by concurrent use of cisplatin in sequential biopsy specimens from patients with cervical cancer.

doi: 10.4161/cbt.6.6.4098

Figure Lengend Snippet: Figure 2. Expression values of four CRT-responsive genes evaluated by microarray in pretreatment (pre) and midtreatment (mid) samples. Normalized expression values are shown for CDKN1A, BAX, TNFSF8 and RRM2B in 19 CRT cases and 20 RT cases. The open circle indicates a patient with a p53 mutation. Significant upregu‑ lation of these genes was induced by CRT. RT-treated samples showed variation between patients in the change of expression of these genes.

Article Snippet: They were stained with Cy5‐streptavidin (Amersham Biosciences) and scanned using a dual‐laser microarray scanner (Agilent).

Techniques: Expressing, Microarray, Mutagenesis

Tissue microarrays of normal tissues and tumors of the respective tissue. First and third lane: normal tissue; second and fourth lane: tumors of the same type of tissue as the normal tissue above. Microarrays containing frozen sections of various tissue samples were purchased from BioCat (Heidelberg, Germany). In brief, the sections were treated with 0.3% H2O2 for 30 min at room temperature (RT). After washing with PBS, the sections were blocked with 10% normal bovine serum for 1 h at RT and subsequently stained with a rabbit anti-human-β2-adrenoceptor antibody (a Santa Cruz Biotechnology, Santa Cruz, CA) and a mouse anti-human neurofilament protein antibody (b Dako Cytomatation, Hamburg, Germany) at 4°C overnight. After washing with PBS, the arrays were incubated with a Cy3-coupled secondary goat anti-rabbit or anti-mouse antibody (Dianova, Hamburg, Germany) for 1 h at RT, and the fluorescence of the samples was analyzed using a dual-laser microarray scanner. In (c), the respective tissue origin is shown

Journal: Cancer Immunology, Immunotherapy : CII

Article Title: Tumor immune escape mechanisms: impact of the neuroendocrine system

doi: 10.1007/s00262-006-0126-x

Figure Lengend Snippet: Tissue microarrays of normal tissues and tumors of the respective tissue. First and third lane: normal tissue; second and fourth lane: tumors of the same type of tissue as the normal tissue above. Microarrays containing frozen sections of various tissue samples were purchased from BioCat (Heidelberg, Germany). In brief, the sections were treated with 0.3% H2O2 for 30 min at room temperature (RT). After washing with PBS, the sections were blocked with 10% normal bovine serum for 1 h at RT and subsequently stained with a rabbit anti-human-β2-adrenoceptor antibody (a Santa Cruz Biotechnology, Santa Cruz, CA) and a mouse anti-human neurofilament protein antibody (b Dako Cytomatation, Hamburg, Germany) at 4°C overnight. After washing with PBS, the arrays were incubated with a Cy3-coupled secondary goat anti-rabbit or anti-mouse antibody (Dianova, Hamburg, Germany) for 1 h at RT, and the fluorescence of the samples was analyzed using a dual-laser microarray scanner. In (c), the respective tissue origin is shown

Article Snippet: After washing with PBS, the arrays were incubated with a Cy3-coupled secondary goat anti-rabbit or anti-mouse antibody (Dianova, Hamburg, Germany) for 1 h at RT, and the fluorescence of the samples was analyzed using a dual-laser microarray scanner.

Techniques: Staining, Incubation, Fluorescence, Microarray