seldi protein chip arrays Search Results


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Ciphergen inc proteinchip seldi system series 4000
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Ciphergen inc surface-enhanced laser desorption-ionization (seldi) protein chipr
Surface Enhanced Laser Desorption Ionization (Seldi) Protein Chipr, 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 protein chip
Seldi Protein Chip, 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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Bio-Rad seldi enterprise edition protein chip reader
Seldi Enterprise Edition Protein Chip Reader, supplied by Bio-Rad, 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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Bio-Rad protein chip seldi system
Protein Chip Seldi System, supplied by Bio-Rad, 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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Bio-Rad seldi-tof protein chip assay
Seldi Tof Protein Chip Assay, supplied by Bio-Rad, 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 pbs ii+ seldi-tof-ms
<t>SELDI-TOF-MS</t> analysis of proteins or peptide segments with an m / z of 9348 Da in the normal and HB groups.
Pbs Ii+ 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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Bio-Rad seldi protein chip arrays
Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization <t>time-of-flight</t> <t>(SELDI-TOF)</t> mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.
Seldi Protein Chip Arrays, supplied by Bio-Rad, 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 proteinchipreader pbs iic
Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization <t>time-of-flight</t> <t>(SELDI-TOF)</t> mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.
Proteinchipreader Pbs Iic, 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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Bio-Rad seldi protein arrays biology system reader 4,000
Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization <t>time-of-flight</t> <t>(SELDI-TOF)</t> mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.
Seldi Protein Arrays Biology System Reader 4,000, supplied by Bio-Rad, 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 protein biology system ii seldi-tof mass spectrometer
Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization <t>time-of-flight</t> <t>(SELDI-TOF)</t> mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.
Protein Biology System Ii Seldi 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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Image Search Results


SELDI-TOF-MS analysis of proteins or peptide segments with an m / z of 9348 Da in the normal and HB groups.

Journal: International Journal of Molecular Sciences

Article Title: Detection of Serum Protein Biomarkers for the Diagnosis and Staging of Hepatoblastoma

doi: 10.3390/ijms160612669

Figure Lengend Snippet: SELDI-TOF-MS analysis of proteins or peptide segments with an m / z of 9348 Da in the normal and HB groups.

Article Snippet: WCX2 Protein Chip, Ciphergen Biosystems Inc., Fremont, CA, USA; PBS II+ SELDI-TOF-MS, Ciphergen Biosystems Inc.; Bioprocessor, Ciphergen Biosystems Inc.; SPD SpeedVac, Thermo Electron Inc., Waltham, MA, USA; High performance liquid chromatography, Shimadzu Inc., Kyoto, Japan; Trypsin, Promega Inc., Madison, WI, USA; MALDI-TOF-TOF, Bruker Inc., Karlsruhe, Germany; 2D-LC-LTQ-MS, Thermo Electron Inc.; Human Apo A–I ELISA Kit, BOSTER, Wuhan, China; Thermo Scientific Varioskan Flash, Thermo Electron Inc.

Techniques:

 SELDI-TOF-MS  mass spectrometry analysis of proteins or peptide segments with an m / z of 9348 Da in the normal and HB groups.

Journal: International Journal of Molecular Sciences

Article Title: Detection of Serum Protein Biomarkers for the Diagnosis and Staging of Hepatoblastoma

doi: 10.3390/ijms160612669

Figure Lengend Snippet: SELDI-TOF-MS mass spectrometry analysis of proteins or peptide segments with an m / z of 9348 Da in the normal and HB groups.

Article Snippet: WCX2 Protein Chip, Ciphergen Biosystems Inc., Fremont, CA, USA; PBS II+ SELDI-TOF-MS, Ciphergen Biosystems Inc.; Bioprocessor, Ciphergen Biosystems Inc.; SPD SpeedVac, Thermo Electron Inc., Waltham, MA, USA; High performance liquid chromatography, Shimadzu Inc., Kyoto, Japan; Trypsin, Promega Inc., Madison, WI, USA; MALDI-TOF-TOF, Bruker Inc., Karlsruhe, Germany; 2D-LC-LTQ-MS, Thermo Electron Inc.; Human Apo A–I ELISA Kit, BOSTER, Wuhan, China; Thermo Scientific Varioskan Flash, Thermo Electron Inc.

Techniques: Mass Spectrometry

Isolation and purification of the proteins or peptide segments with an m / z of 9348 Da by HPLC. MALDI-TOF-MS confirmed that the sample eluted at minutes 36 and 37 contained the proteins with an m / z of 9348 Da.

Journal: International Journal of Molecular Sciences

Article Title: Detection of Serum Protein Biomarkers for the Diagnosis and Staging of Hepatoblastoma

doi: 10.3390/ijms160612669

Figure Lengend Snippet: Isolation and purification of the proteins or peptide segments with an m / z of 9348 Da by HPLC. MALDI-TOF-MS confirmed that the sample eluted at minutes 36 and 37 contained the proteins with an m / z of 9348 Da.

Article Snippet: WCX2 Protein Chip, Ciphergen Biosystems Inc., Fremont, CA, USA; PBS II+ SELDI-TOF-MS, Ciphergen Biosystems Inc.; Bioprocessor, Ciphergen Biosystems Inc.; SPD SpeedVac, Thermo Electron Inc., Waltham, MA, USA; High performance liquid chromatography, Shimadzu Inc., Kyoto, Japan; Trypsin, Promega Inc., Madison, WI, USA; MALDI-TOF-TOF, Bruker Inc., Karlsruhe, Germany; 2D-LC-LTQ-MS, Thermo Electron Inc.; Human Apo A–I ELISA Kit, BOSTER, Wuhan, China; Thermo Scientific Varioskan Flash, Thermo Electron Inc.

Techniques: Isolation, Purification

Isolation and purification of the proteins or peptide segments with an m / z of 9348 Da by HPLC. MALDI-TOF-MS confirmed that the sample eluted at minutes 36 and 37 contained the proteins with an m / z of 9348 Da.

Journal: International Journal of Molecular Sciences

Article Title: Detection of Serum Protein Biomarkers for the Diagnosis and Staging of Hepatoblastoma

doi: 10.3390/ijms160612669

Figure Lengend Snippet: Isolation and purification of the proteins or peptide segments with an m / z of 9348 Da by HPLC. MALDI-TOF-MS confirmed that the sample eluted at minutes 36 and 37 contained the proteins with an m / z of 9348 Da.

Article Snippet: WCX2 Protein Chip, Ciphergen Biosystems Inc., Fremont, CA, USA; PBS II+ SELDI-TOF-MS, Ciphergen Biosystems Inc.; Bioprocessor, Ciphergen Biosystems Inc.; SPD SpeedVac, Thermo Electron Inc., Waltham, MA, USA; High performance liquid chromatography, Shimadzu Inc., Kyoto, Japan; Trypsin, Promega Inc., Madison, WI, USA; MALDI-TOF-TOF, Bruker Inc., Karlsruhe, Germany; 2D-LC-LTQ-MS, Thermo Electron Inc.; Human Apo A–I ELISA Kit, BOSTER, Wuhan, China; Thermo Scientific Varioskan Flash, Thermo Electron Inc.

Techniques: Isolation, Purification

Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization time-of-flight (SELDI-TOF) mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.

Journal: Breast Cancer Research : BCR

Article Title: Novel serum protein biomarker panel revealed by mass spectrometry and its prognostic value in breast cancer

doi: 10.1186/bcr3676

Figure Lengend Snippet: Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization time-of-flight (SELDI-TOF) mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.

Article Snippet: All serum samples were initially denatured in buffer containing 8 M urea, 1% CHAPS (3-[(3-cholamidopropyl) dimethylammonio]-1-propanesulfate) and analyzed by TOF MS on SELDI protein chip arrays (Bio-Rad, Hercules, CA, USA) as previously described [ ].

Techniques: Western Blot, Mass Spectrometry, Standard Deviation, Derivative Assay