mass array compact maldi tof Search Results


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Ciphergen inc maldi-tof mass spectrometer
Examples of <t>typical</t> <t>SELDI-TOF</t> <t>MS</t> spectra obtained from the lysates of anaerobically and aerobically cultured cells.
Maldi Tof Mass Spectrometer, supplied by Ciphergen 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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BGI Shenzhen pcr based maldi-tof assay
Examples of <t>typical</t> <t>SELDI-TOF</t> <t>MS</t> spectra obtained from the lysates of anaerobically and aerobically cultured cells.
Pcr Based Maldi Tof Assay, supplied by BGI Shenzhen, 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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Ciphergen inc seldi-tof-ms reader
Expression of the yciGFE locus in E. coli K-12 strains. A, <t>SELDI-TOF-MS</t> profiles of E. coli MG1655 and its mutant derivatives using the Q10 ProteinChip array. Clear lysates from MG1655 (WT) and its mutants MG655hns, MG1655hnsyciE, and MG1655hnsyciF were applied to the surface of a Q10 ProteinChip as described in the Experimental Procedures section. The captured proteins were detected using surface enhanced laser desorption/ionization (SELDI) time-of-flight mass spectrometry. Normalized mass (m/z) for each peak (in Daltons (Da)) is demonstrated on the x-axis, whereas intensity (μA) is plotted on the y-axis. A laser energy of 3200 nJ was used. The relevant portion of the spectra is shown. The arrows indicate the YciE and YciF proteins. B, Expression of the yciE-lacZ fusion in the E. coli strains indicated was determined in overnight LB cultures at 37 °C. Lanes 1 to 5: (1) MC4100 yciE-lacZ, (2) MC4100hns yciE-lacZ, (3) MC4100mcbR yciE-lacZ, (4) MC4100hnsmcbR yciE-lacZ, (5) MC4100hnsrpoS yciE-lacZ. Lanes 6 to 15: MC4100 yciE-lacZ harboring pCABg (6), pmcbRHIS (7), pQE30 (12), and pyncCHIS (13); MC4100hns yciE-lacZ harboring pCABg (8), pmcbRHIS (9), pQE30 (14), and pyncCHIS (15); and MC4100hnsmcbR yciE-lacZ harboring pCABg (10), and pmcbRHIS (11).
Seldi Tof Ms Reader, supplied by Ciphergen 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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Sony 4 × 12 array disposable maldi plate
Expression of the yciGFE locus in E. coli K-12 strains. A, <t>SELDI-TOF-MS</t> profiles of E. coli MG1655 and its mutant derivatives using the Q10 ProteinChip array. Clear lysates from MG1655 (WT) and its mutants MG655hns, MG1655hnsyciE, and MG1655hnsyciF were applied to the surface of a Q10 ProteinChip as described in the Experimental Procedures section. The captured proteins were detected using surface enhanced laser desorption/ionization (SELDI) time-of-flight mass spectrometry. Normalized mass (m/z) for each peak (in Daltons (Da)) is demonstrated on the x-axis, whereas intensity (μA) is plotted on the y-axis. A laser energy of 3200 nJ was used. The relevant portion of the spectra is shown. The arrows indicate the YciE and YciF proteins. B, Expression of the yciE-lacZ fusion in the E. coli strains indicated was determined in overnight LB cultures at 37 °C. Lanes 1 to 5: (1) MC4100 yciE-lacZ, (2) MC4100hns yciE-lacZ, (3) MC4100mcbR yciE-lacZ, (4) MC4100hnsmcbR yciE-lacZ, (5) MC4100hnsrpoS yciE-lacZ. Lanes 6 to 15: MC4100 yciE-lacZ harboring pCABg (6), pmcbRHIS (7), pQE30 (12), and pyncCHIS (13); MC4100hns yciE-lacZ harboring pCABg (8), pmcbRHIS (9), pQE30 (14), and pyncCHIS (15); and MC4100hnsmcbR yciE-lacZ harboring pCABg (10), and pmcbRHIS (11).
4 × 12 Array Disposable Maldi Plate, supplied by Sony, 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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Ciphergen inc pcs4000 seldi-tof ms proteinchip reader
Expression of the yciGFE locus in E. coli K-12 strains. A, <t>SELDI-TOF-MS</t> profiles of E. coli MG1655 and its mutant derivatives using the Q10 ProteinChip array. Clear lysates from MG1655 (WT) and its mutants MG655hns, MG1655hnsyciE, and MG1655hnsyciF were applied to the surface of a Q10 ProteinChip as described in the Experimental Procedures section. The captured proteins were detected using surface enhanced laser desorption/ionization (SELDI) time-of-flight mass spectrometry. Normalized mass (m/z) for each peak (in Daltons (Da)) is demonstrated on the x-axis, whereas intensity (μA) is plotted on the y-axis. A laser energy of 3200 nJ was used. The relevant portion of the spectra is shown. The arrows indicate the YciE and YciF proteins. B, Expression of the yciE-lacZ fusion in the E. coli strains indicated was determined in overnight LB cultures at 37 °C. Lanes 1 to 5: (1) MC4100 yciE-lacZ, (2) MC4100hns yciE-lacZ, (3) MC4100mcbR yciE-lacZ, (4) MC4100hnsmcbR yciE-lacZ, (5) MC4100hnsrpoS yciE-lacZ. Lanes 6 to 15: MC4100 yciE-lacZ harboring pCABg (6), pmcbRHIS (7), pQE30 (12), and pyncCHIS (13); MC4100hns yciE-lacZ harboring pCABg (8), pmcbRHIS (9), pQE30 (14), and pyncCHIS (15); and MC4100hnsmcbR yciE-lacZ harboring pCABg (10), and pmcbRHIS (11).
Pcs4000 Seldi Tof Ms Proteinchip Reader, supplied by Ciphergen 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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Ciphergen inc seldi-tof ms
Expression of the yciGFE locus in E. coli K-12 strains. A, <t>SELDI-TOF-MS</t> profiles of E. coli MG1655 and its mutant derivatives using the Q10 ProteinChip array. Clear lysates from MG1655 (WT) and its mutants MG655hns, MG1655hnsyciE, and MG1655hnsyciF were applied to the surface of a Q10 ProteinChip as described in the Experimental Procedures section. The captured proteins were detected using surface enhanced laser desorption/ionization (SELDI) time-of-flight mass spectrometry. Normalized mass (m/z) for each peak (in Daltons (Da)) is demonstrated on the x-axis, whereas intensity (μA) is plotted on the y-axis. A laser energy of 3200 nJ was used. The relevant portion of the spectra is shown. The arrows indicate the YciE and YciF proteins. B, Expression of the yciE-lacZ fusion in the E. coli strains indicated was determined in overnight LB cultures at 37 °C. Lanes 1 to 5: (1) MC4100 yciE-lacZ, (2) MC4100hns yciE-lacZ, (3) MC4100mcbR yciE-lacZ, (4) MC4100hnsmcbR yciE-lacZ, (5) MC4100hnsrpoS yciE-lacZ. Lanes 6 to 15: MC4100 yciE-lacZ harboring pCABg (6), pmcbRHIS (7), pQE30 (12), and pyncCHIS (13); MC4100hns yciE-lacZ harboring pCABg (8), pmcbRHIS (9), pQE30 (14), and pyncCHIS (15); and MC4100hnsmcbR yciE-lacZ harboring pCABg (10), and pmcbRHIS (11).
Seldi Tof Ms, supplied by Ciphergen 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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Ciphergen inc proteinchip reader
Expression of the yciGFE locus in E. coli K-12 strains. A, <t>SELDI-TOF-MS</t> profiles of E. coli MG1655 and its mutant derivatives using the Q10 ProteinChip array. Clear lysates from MG1655 (WT) and its mutants MG655hns, MG1655hnsyciE, and MG1655hnsyciF were applied to the surface of a Q10 ProteinChip as described in the Experimental Procedures section. The captured proteins were detected using surface enhanced laser desorption/ionization (SELDI) time-of-flight mass spectrometry. Normalized mass (m/z) for each peak (in Daltons (Da)) is demonstrated on the x-axis, whereas intensity (μA) is plotted on the y-axis. A laser energy of 3200 nJ was used. The relevant portion of the spectra is shown. The arrows indicate the YciE and YciF proteins. B, Expression of the yciE-lacZ fusion in the E. coli strains indicated was determined in overnight LB cultures at 37 °C. Lanes 1 to 5: (1) MC4100 yciE-lacZ, (2) MC4100hns yciE-lacZ, (3) MC4100mcbR yciE-lacZ, (4) MC4100hnsmcbR yciE-lacZ, (5) MC4100hnsrpoS yciE-lacZ. Lanes 6 to 15: MC4100 yciE-lacZ harboring pCABg (6), pmcbRHIS (7), pQE30 (12), and pyncCHIS (13); MC4100hns yciE-lacZ harboring pCABg (8), pmcbRHIS (9), pQE30 (14), and pyncCHIS (15); and MC4100hnsmcbR yciE-lacZ harboring pCABg (10), and pmcbRHIS (11).
Proteinchip Reader, supplied by Ciphergen 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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Verlag GmbH microarrays for mass spectrometry (mams)
Expression of the yciGFE locus in E. coli K-12 strains. A, <t>SELDI-TOF-MS</t> profiles of E. coli MG1655 and its mutant derivatives using the Q10 ProteinChip array. Clear lysates from MG1655 (WT) and its mutants MG655hns, MG1655hnsyciE, and MG1655hnsyciF were applied to the surface of a Q10 ProteinChip as described in the Experimental Procedures section. The captured proteins were detected using surface enhanced laser desorption/ionization (SELDI) time-of-flight mass spectrometry. Normalized mass (m/z) for each peak (in Daltons (Da)) is demonstrated on the x-axis, whereas intensity (μA) is plotted on the y-axis. A laser energy of 3200 nJ was used. The relevant portion of the spectra is shown. The arrows indicate the YciE and YciF proteins. B, Expression of the yciE-lacZ fusion in the E. coli strains indicated was determined in overnight LB cultures at 37 °C. Lanes 1 to 5: (1) MC4100 yciE-lacZ, (2) MC4100hns yciE-lacZ, (3) MC4100mcbR yciE-lacZ, (4) MC4100hnsmcbR yciE-lacZ, (5) MC4100hnsrpoS yciE-lacZ. Lanes 6 to 15: MC4100 yciE-lacZ harboring pCABg (6), pmcbRHIS (7), pQE30 (12), and pyncCHIS (13); MC4100hns yciE-lacZ harboring pCABg (8), pmcbRHIS (9), pQE30 (14), and pyncCHIS (15); and MC4100hnsmcbR yciE-lacZ harboring pCABg (10), and pmcbRHIS (11).
Microarrays For Mass Spectrometry (Mams), supplied by Verlag 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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Image Search Results


Examples of typical SELDI-TOF MS spectra obtained from the lysates of anaerobically and aerobically cultured cells.

Journal: BioMed Research International

Article Title: Correlation between Phylogroups and Intracellular Proteomes of Propionibacterium acnes and Differences in the Protein Expression Profiles between Anaerobically and Aerobically Grown Cells

doi: 10.1155/2013/151797

Figure Lengend Snippet: Examples of typical SELDI-TOF MS spectra obtained from the lysates of anaerobically and aerobically cultured cells.

Article Snippet: The ProteinChip arrays were analysed in a MALDI-TOF mass spectrometer (Ciphergen BioSystems, Model PBS II) according to an automated data collection protocol [ ].

Techniques: Cell Culture

Heat map of SELDI-TOF MS spectra generated from 42 protein samples (anaerobically and aerobically grown cells of 21 P. acnes strains). All mass ions from each spectrum were analysed using the Ciphergen Biosystems Express Heat Map Software . This software allowed comparison of mass ions ( m/z ) between various samples and presents the data both as a dendrogram and heat map. The coloured boxes represent intensity of each peak in the SELDI spectra and each colour intensity of the green and the red indicates the difference from the average peak intensity.

Journal: BioMed Research International

Article Title: Correlation between Phylogroups and Intracellular Proteomes of Propionibacterium acnes and Differences in the Protein Expression Profiles between Anaerobically and Aerobically Grown Cells

doi: 10.1155/2013/151797

Figure Lengend Snippet: Heat map of SELDI-TOF MS spectra generated from 42 protein samples (anaerobically and aerobically grown cells of 21 P. acnes strains). All mass ions from each spectrum were analysed using the Ciphergen Biosystems Express Heat Map Software . This software allowed comparison of mass ions ( m/z ) between various samples and presents the data both as a dendrogram and heat map. The coloured boxes represent intensity of each peak in the SELDI spectra and each colour intensity of the green and the red indicates the difference from the average peak intensity.

Article Snippet: The ProteinChip arrays were analysed in a MALDI-TOF mass spectrometer (Ciphergen BioSystems, Model PBS II) according to an automated data collection protocol [ ].

Techniques: Generated, Software

Expression of the yciGFE locus in E. coli K-12 strains. A, SELDI-TOF-MS profiles of E. coli MG1655 and its mutant derivatives using the Q10 ProteinChip array. Clear lysates from MG1655 (WT) and its mutants MG655hns, MG1655hnsyciE, and MG1655hnsyciF were applied to the surface of a Q10 ProteinChip as described in the Experimental Procedures section. The captured proteins were detected using surface enhanced laser desorption/ionization (SELDI) time-of-flight mass spectrometry. Normalized mass (m/z) for each peak (in Daltons (Da)) is demonstrated on the x-axis, whereas intensity (μA) is plotted on the y-axis. A laser energy of 3200 nJ was used. The relevant portion of the spectra is shown. The arrows indicate the YciE and YciF proteins. B, Expression of the yciE-lacZ fusion in the E. coli strains indicated was determined in overnight LB cultures at 37 °C. Lanes 1 to 5: (1) MC4100 yciE-lacZ, (2) MC4100hns yciE-lacZ, (3) MC4100mcbR yciE-lacZ, (4) MC4100hnsmcbR yciE-lacZ, (5) MC4100hnsrpoS yciE-lacZ. Lanes 6 to 15: MC4100 yciE-lacZ harboring pCABg (6), pmcbRHIS (7), pQE30 (12), and pyncCHIS (13); MC4100hns yciE-lacZ harboring pCABg (8), pmcbRHIS (9), pQE30 (14), and pyncCHIS (15); and MC4100hnsmcbR yciE-lacZ harboring pCABg (10), and pmcbRHIS (11).

Journal: Molecular & Cellular Proteomics : MCP

Article Title: A Proteomic Analysis Reveals Differential Regulation of the ? S -Dependent yciGFE ( katN ) Locus by YncC and H-NS in Salmonella and Escherichia coli K-12

doi: 10.1074/mcp.M110.002493

Figure Lengend Snippet: Expression of the yciGFE locus in E. coli K-12 strains. A, SELDI-TOF-MS profiles of E. coli MG1655 and its mutant derivatives using the Q10 ProteinChip array. Clear lysates from MG1655 (WT) and its mutants MG655hns, MG1655hnsyciE, and MG1655hnsyciF were applied to the surface of a Q10 ProteinChip as described in the Experimental Procedures section. The captured proteins were detected using surface enhanced laser desorption/ionization (SELDI) time-of-flight mass spectrometry. Normalized mass (m/z) for each peak (in Daltons (Da)) is demonstrated on the x-axis, whereas intensity (μA) is plotted on the y-axis. A laser energy of 3200 nJ was used. The relevant portion of the spectra is shown. The arrows indicate the YciE and YciF proteins. B, Expression of the yciE-lacZ fusion in the E. coli strains indicated was determined in overnight LB cultures at 37 °C. Lanes 1 to 5: (1) MC4100 yciE-lacZ, (2) MC4100hns yciE-lacZ, (3) MC4100mcbR yciE-lacZ, (4) MC4100hnsmcbR yciE-lacZ, (5) MC4100hnsrpoS yciE-lacZ. Lanes 6 to 15: MC4100 yciE-lacZ harboring pCABg (6), pmcbRHIS (7), pQE30 (12), and pyncCHIS (13); MC4100hns yciE-lacZ harboring pCABg (8), pmcbRHIS (9), pQE30 (14), and pyncCHIS (15); and MC4100hnsmcbR yciE-lacZ harboring pCABg (10), and pmcbRHIS (11).

Article Snippet: Molecules retained on the surfaces were visualized by reading the spots of each array in a SELDI-TOF-MS reader (PSC4000; Ciphergen Biosystems, Copenhagen, Denmark).

Techniques: Expressing, Mutagenesis, Mass Spectrometry