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scx chromatography column polysulfethyl 4.6 × column  (Thermo Fisher)
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Thermo Fisher scx chromatography column polysulfethyl 4.6 × column
Scx Chromatography Column Polysulfethyl 4.6 × Column, supplied by Thermo Fisher, 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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1d cation-exchange chromatography (cex) column mabpac scx-10  (Thermo Fisher)
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scx chromatography column: polysulfethyl 4.6 × column  (Thermo Fisher)
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Thermo Fisher scx chromatography column: polysulfethyl 4.6 × column
Scx Chromatography Column: Polysulfethyl 4.6 × Column, supplied by Thermo Fisher, 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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ion-exchange chromatography biobasic-scx column  (Bio Basic Canada)
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scx chromatography column polysulfoethyl  (The Nest Group)
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The sequence of the workflow is indicated by the arrows in the right side. Pooled reference: Small aliquots from each of the 75 samples of amniotic fluid were pooled to create a reference sample. Deplete-concentrate-reduce-block: The amniotic fluid samples were depleted of albumin and IgG, subsequently concentrated and reduced. Digestion: The samples were subjected to trypsin digestion. Labeling: The reference sample and three individual samples (denoted A, B, and C in the figure) were labeled with iTRAQ reagents (the numbers 114–117 refer to the reporter mass of the individual iTRAQ reagent). Mixing and fractionation: The four labeled samples were mixed and subjected to strong cation exchange <t>(SCX)</t> fractionation to simplify the mixture prior to conducting liquid <t>chromatography</t> and mass spectrometry (LC-MS/MS). Each SCX fraction was subjected to LC-MS/MS. Liquid chromatography: Proteins were separated by liquid chromatography. The retention time is displayed in the horizontal axis. MS1: The first stage of mass spectrometry for a specific retention time is indicated schematically. Each peak in the mass spectrum (horizontal axis is m/z) corresponds to an individual peptide. MS2: A single peak is selected for collisional dissociation and the fragments subjected to a second stage mass spectrometry (tandem MS/MS). The reporter ions from the iTRAQ label appear in the low mass range, distinct from peptide fragment peaks. The pattern of peaks in the final mass spectrum is matched to a database in order to identify the parent peptide. The intensities of the reporter ion peaks indicate the relative abundance of the four samples.
Scx Chromatography Column Polysulfoethyl, supplied by The Nest Group, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scx+chromatography+column/scx+column+polysulfoethyl+a/pmc09665101-296-7-12
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scx chromatography column polysulfoethyl - by Bioz Stars, 2026-10
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strong cation exchange chromatography scx column  (Danaher Inc)
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Danaher Inc strong cation exchange chromatography scx column
The sequence of the workflow is indicated by the arrows in the right side. Pooled reference: Small aliquots from each of the 75 samples of amniotic fluid were pooled to create a reference sample. Deplete-concentrate-reduce-block: The amniotic fluid samples were depleted of albumin and IgG, subsequently concentrated and reduced. Digestion: The samples were subjected to trypsin digestion. Labeling: The reference sample and three individual samples (denoted A, B, and C in the figure) were labeled with iTRAQ reagents (the numbers 114–117 refer to the reporter mass of the individual iTRAQ reagent). Mixing and fractionation: The four labeled samples were mixed and subjected to strong cation exchange <t>(SCX)</t> fractionation to simplify the mixture prior to conducting liquid <t>chromatography</t> and mass spectrometry (LC-MS/MS). Each SCX fraction was subjected to LC-MS/MS. Liquid chromatography: Proteins were separated by liquid chromatography. The retention time is displayed in the horizontal axis. MS1: The first stage of mass spectrometry for a specific retention time is indicated schematically. Each peak in the mass spectrum (horizontal axis is m/z) corresponds to an individual peptide. MS2: A single peak is selected for collisional dissociation and the fragments subjected to a second stage mass spectrometry (tandem MS/MS). The reporter ions from the iTRAQ label appear in the low mass range, distinct from peptide fragment peaks. The pattern of peaks in the final mass spectrum is matched to a database in order to identify the parent peptide. The intensities of the reporter ion peaks indicate the relative abundance of the four samples.
Strong Cation Exchange Chromatography Scx Column, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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strong cation exchange chromatography scx column - by Bioz Stars, 2026-10
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strong cation exchange chromatography scx column  (Waters Corporation)
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Waters Corporation strong cation exchange chromatography scx column
The sequence of the workflow is indicated by the arrows in the right side. Pooled reference: Small aliquots from each of the 75 samples of amniotic fluid were pooled to create a reference sample. Deplete-concentrate-reduce-block: The amniotic fluid samples were depleted of albumin and IgG, subsequently concentrated and reduced. Digestion: The samples were subjected to trypsin digestion. Labeling: The reference sample and three individual samples (denoted A, B, and C in the figure) were labeled with iTRAQ reagents (the numbers 114–117 refer to the reporter mass of the individual iTRAQ reagent). Mixing and fractionation: The four labeled samples were mixed and subjected to strong cation exchange <t>(SCX)</t> fractionation to simplify the mixture prior to conducting liquid <t>chromatography</t> and mass spectrometry (LC-MS/MS). Each SCX fraction was subjected to LC-MS/MS. Liquid chromatography: Proteins were separated by liquid chromatography. The retention time is displayed in the horizontal axis. MS1: The first stage of mass spectrometry for a specific retention time is indicated schematically. Each peak in the mass spectrum (horizontal axis is m/z) corresponds to an individual peptide. MS2: A single peak is selected for collisional dissociation and the fragments subjected to a second stage mass spectrometry (tandem MS/MS). The reporter ions from the iTRAQ label appear in the low mass range, distinct from peptide fragment peaks. The pattern of peaks in the final mass spectrum is matched to a database in order to identify the parent peptide. The intensities of the reporter ion peaks indicate the relative abundance of the four samples.
Strong Cation Exchange Chromatography Scx Column, supplied by Waters Corporation, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/scx+chromatography+column/pm34314788-97-8-14
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strong cation exchange chromatography scx column - by Bioz Stars, 2026-10
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scx cartridge column chromatography biotage isolutetm scx-2 (1 g, spe column)  (BIOTAGE)
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BIOTAGE scx cartridge column chromatography biotage isolutetm scx-2 (1 g, spe column)
The sequence of the workflow is indicated by the arrows in the right side. Pooled reference: Small aliquots from each of the 75 samples of amniotic fluid were pooled to create a reference sample. Deplete-concentrate-reduce-block: The amniotic fluid samples were depleted of albumin and IgG, subsequently concentrated and reduced. Digestion: The samples were subjected to trypsin digestion. Labeling: The reference sample and three individual samples (denoted A, B, and C in the figure) were labeled with iTRAQ reagents (the numbers 114–117 refer to the reporter mass of the individual iTRAQ reagent). Mixing and fractionation: The four labeled samples were mixed and subjected to strong cation exchange <t>(SCX)</t> fractionation to simplify the mixture prior to conducting liquid <t>chromatography</t> and mass spectrometry (LC-MS/MS). Each SCX fraction was subjected to LC-MS/MS. Liquid chromatography: Proteins were separated by liquid chromatography. The retention time is displayed in the horizontal axis. MS1: The first stage of mass spectrometry for a specific retention time is indicated schematically. Each peak in the mass spectrum (horizontal axis is m/z) corresponds to an individual peptide. MS2: A single peak is selected for collisional dissociation and the fragments subjected to a second stage mass spectrometry (tandem MS/MS). The reporter ions from the iTRAQ label appear in the low mass range, distinct from peptide fragment peaks. The pattern of peaks in the final mass spectrum is matched to a database in order to identify the parent peptide. The intensities of the reporter ion peaks indicate the relative abundance of the four samples.
Scx Cartridge Column Chromatography Biotage Isolutetm Scx 2 (1 G, Spe Column), supplied by BIOTAGE, 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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scx cartridge column chromatography biotage isolutetm scx-2 (1 g, spe column) - by Bioz Stars, 2026-10
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supelcosil liquid chromatography-scx column  (Millipore)
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Millipore supelcosil liquid chromatography-scx column
The sequence of the workflow is indicated by the arrows in the right side. Pooled reference: Small aliquots from each of the 75 samples of amniotic fluid were pooled to create a reference sample. Deplete-concentrate-reduce-block: The amniotic fluid samples were depleted of albumin and IgG, subsequently concentrated and reduced. Digestion: The samples were subjected to trypsin digestion. Labeling: The reference sample and three individual samples (denoted A, B, and C in the figure) were labeled with iTRAQ reagents (the numbers 114–117 refer to the reporter mass of the individual iTRAQ reagent). Mixing and fractionation: The four labeled samples were mixed and subjected to strong cation exchange <t>(SCX)</t> fractionation to simplify the mixture prior to conducting liquid <t>chromatography</t> and mass spectrometry (LC-MS/MS). Each SCX fraction was subjected to LC-MS/MS. Liquid chromatography: Proteins were separated by liquid chromatography. The retention time is displayed in the horizontal axis. MS1: The first stage of mass spectrometry for a specific retention time is indicated schematically. Each peak in the mass spectrum (horizontal axis is m/z) corresponds to an individual peptide. MS2: A single peak is selected for collisional dissociation and the fragments subjected to a second stage mass spectrometry (tandem MS/MS). The reporter ions from the iTRAQ label appear in the low mass range, distinct from peptide fragment peaks. The pattern of peaks in the final mass spectrum is matched to a database in order to identify the parent peptide. The intensities of the reporter ion peaks indicate the relative abundance of the four samples.
Supelcosil Liquid Chromatography Scx Column, supplied by Millipore, 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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supelcosil liquid chromatography-scx column - by Bioz Stars, 2026-10
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The sequence of the workflow is indicated by the arrows in the right side. Pooled reference: Small aliquots from each of the 75 samples of amniotic fluid were pooled to create a reference sample. Deplete-concentrate-reduce-block: The amniotic fluid samples were depleted of albumin and IgG, subsequently concentrated and reduced. Digestion: The samples were subjected to trypsin digestion. Labeling: The reference sample and three individual samples (denoted A, B, and C in the figure) were labeled with iTRAQ reagents (the numbers 114–117 refer to the reporter mass of the individual iTRAQ reagent). Mixing and fractionation: The four labeled samples were mixed and subjected to strong cation exchange (SCX) fractionation to simplify the mixture prior to conducting liquid chromatography and mass spectrometry (LC-MS/MS). Each SCX fraction was subjected to LC-MS/MS. Liquid chromatography: Proteins were separated by liquid chromatography. The retention time is displayed in the horizontal axis. MS1: The first stage of mass spectrometry for a specific retention time is indicated schematically. Each peak in the mass spectrum (horizontal axis is m/z) corresponds to an individual peptide. MS2: A single peak is selected for collisional dissociation and the fragments subjected to a second stage mass spectrometry (tandem MS/MS). The reporter ions from the iTRAQ label appear in the low mass range, distinct from peptide fragment peaks. The pattern of peaks in the final mass spectrum is matched to a database in order to identify the parent peptide. The intensities of the reporter ion peaks indicate the relative abundance of the four samples.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians

Article Title: Isobaric labeling and tandem mass spectrometry: a novel approach for profiling and quantifying proteins differentially expressed in amniotic fluid in preterm labor with and without intra-amniotic infection/inflammation

doi: 10.3109/14767050903067386

Figure Lengend Snippet: The sequence of the workflow is indicated by the arrows in the right side. Pooled reference: Small aliquots from each of the 75 samples of amniotic fluid were pooled to create a reference sample. Deplete-concentrate-reduce-block: The amniotic fluid samples were depleted of albumin and IgG, subsequently concentrated and reduced. Digestion: The samples were subjected to trypsin digestion. Labeling: The reference sample and three individual samples (denoted A, B, and C in the figure) were labeled with iTRAQ reagents (the numbers 114–117 refer to the reporter mass of the individual iTRAQ reagent). Mixing and fractionation: The four labeled samples were mixed and subjected to strong cation exchange (SCX) fractionation to simplify the mixture prior to conducting liquid chromatography and mass spectrometry (LC-MS/MS). Each SCX fraction was subjected to LC-MS/MS. Liquid chromatography: Proteins were separated by liquid chromatography. The retention time is displayed in the horizontal axis. MS1: The first stage of mass spectrometry for a specific retention time is indicated schematically. Each peak in the mass spectrum (horizontal axis is m/z) corresponds to an individual peptide. MS2: A single peak is selected for collisional dissociation and the fragments subjected to a second stage mass spectrometry (tandem MS/MS). The reporter ions from the iTRAQ label appear in the low mass range, distinct from peptide fragment peaks. The pattern of peaks in the final mass spectrum is matched to a database in order to identify the parent peptide. The intensities of the reporter ion peaks indicate the relative abundance of the four samples.

Article Snippet: Each peptide mixture was separated on an SCX chromatography column (Polysulfoethyl column, The Nest Group Inc, Southborough, MA USA).

Techniques: Sequencing, Blocking Assay, Labeling, Multiplex sample analysis, Fractionation, Liquid Chromatography, Mass Spectrometry, Liquid Chromatography with Mass Spectroscopy, Tandem Mass Spectroscopy