tio2 column chromatography Search Results


90
Huntsman International LLC tio2 support tp hombikat
Tio2 Support Tp Hombikat, supplied by Huntsman International LLC, 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/tio2+column+chromatography/tio2/us11279667-213-4-8
Average 90 stars, based on 1 article reviews
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99
JASCO Inc hplc analysis
Hplc Analysis, supplied by JASCO Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tio2+column+chromatography/JASCO+HPLC/us07186768-272-32-37
Average 99 stars, based on 1 article reviews
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90
GL Sciences chromatographic phospholipid trap column tio 2
Chromatographic Phospholipid Trap Column Tio 2, supplied by GL Sciences, 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/tio2+column+chromatography/tio+2+beads/pmc09909672-16-3-21
Average 90 stars, based on 1 article reviews
chromatographic phospholipid trap column tio 2 - by Bioz Stars, 2026-09
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97
Thermo Fisher tio 2 column chromatography
Tio 2 Column Chromatography, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tio2+column+chromatography/TIOTROPIUM+BROMIDE/pmc11048773-55-15-19
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tio 2 column chromatography - by Bioz Stars, 2026-09
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90
GL Sciences titanium dioxide chromatography titanosphere phos-tio kit
Titanium Dioxide Chromatography Titanosphere Phos Tio Kit, supplied by GL Sciences, 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/tio2+column+chromatography/titanium+dioxide+chromatography+titanosphere+phos+tio+kit/pmc04565165-122-4-21
Average 90 stars, based on 1 article reviews
titanium dioxide chromatography titanosphere phos-tio kit - by Bioz Stars, 2026-09
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90
Maisch GmbH tio 2 beads
Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the <t>non-phosphorylated</t> peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.
Tio 2 Beads, supplied by Maisch GmbH, 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/tio2+column+chromatography/tio+2+beads/pmc04288255-106-33-53
Average 90 stars, based on 1 article reviews
tio 2 beads - by Bioz Stars, 2026-09
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90
Dr Maisch HPLC c18 column
Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the <t>non-phosphorylated</t> peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.
C18 Column, supplied by Dr Maisch HPLC, 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/tio2+column+chromatography/c18+column/pmc03079584__pbio__1000611__s019-55-6-23
Average 90 stars, based on 1 article reviews
c18 column - by Bioz Stars, 2026-09
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90
GL Sciences titanium dioxide chromatography titanosphere phos-tiokit
Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the <t>non-phosphorylated</t> peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.
Titanium Dioxide Chromatography Titanosphere Phos Tiokit, supplied by GL Sciences, 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/tio2+column+chromatography/titanium+dioxide+chromatography+titanosphere+phos+tiokit/10__1074_slash_mcp__m113__035485-75-4-18
Average 90 stars, based on 1 article reviews
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90
GL Sciences titanosphere phos-tio kit
Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the <t>non-phosphorylated</t> peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.
Titanosphere Phos Tio Kit, supplied by GL Sciences, 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/tio2+column+chromatography/titanosphere+phos+tio+kit/pmc04565165-68-15-21
Average 90 stars, based on 1 article reviews
titanosphere phos-tio kit - by Bioz Stars, 2026-09
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90
GL Sciences zro 2 powder
Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the <t>non-phosphorylated</t> peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.
Zro 2 Powder, supplied by GL Sciences, 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/tio2+column+chromatography/zro2/pmc05995969-363-29-24
Average 90 stars, based on 1 article reviews
zro 2 powder - by Bioz Stars, 2026-09
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90
PolyLC INC polylc column
Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the <t>non-phosphorylated</t> peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.
Polylc Column, supplied by PolyLC INC, 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/tio2+column+chromatography/polylc+column/pmc03645873-247-44-44
Average 90 stars, based on 1 article reviews
polylc column - by Bioz Stars, 2026-09
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97
Spirochrome sir-actin
Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the <t>non-phosphorylated</t> peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.
Sir Actin, supplied by Spirochrome, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tio2+column+chromatography/SiR-actin/custom%40sc001%4028280093
Average 97 stars, based on 1 article reviews
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Image Search Results


Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the non-phosphorylated peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.

Journal: Molecular & Cellular Proteomics : MCP

Article Title: Comprehensive and Reproducible Phosphopeptide Enrichment Using Iron Immobilized Metal Ion Affinity Chromatography (Fe-IMAC) Columns

doi: 10.1074/mcp.M114.043109

Figure Lengend Snippet: Fe-IMAC column characterization. A, Fe-IMAC UV chromatogram of 1 mg of A431 cell digest. The phosphopeptide fraction (reaction time: ∼49 min) is well separated from the column breakthrough that contains the non-phosphorylated peptides. The inset on the left shows the number of phosphopeptides identified from the IMAC eluate and the number of phosphopeptides identified from a second IMAC enrichment of the column flow-through (FT) of the first Fe-IMAC enrichment. The inset on the right shows the respective UV traces. Both indicate that the A431 digest was essentially depleted of phosphopeptides. B, UV signal-based quantification of Fe-IMAC enriched phosphopeptides as a function of the amount of cellular digest applied. It is apparent that the column captured phosphopeptides over a wide linear range. C, Venn diagram of the number of unique phosphopeptide identifications across three technical replicates of Fe-IMAC purification of phosphopeptides from 1 mg of A431 lysate digest.

Article Snippet: The supernatant was quenched by the addition of 30 μl of 100% FA, dried down, and stored at −80 °C. . Phosphopeptide Enrichment with TiO 2 and Ti-IMAC Columns For chromatographic separation of phosphorylated peptides, TiO 2 beads (5 μm; GL Sciences Inc.) were packed into a column (10 × 4 mm; Dr. Maisch, Ammerbuch, Germany; Amersham Biosciences) and connected to an HPLC system (ÄKTA Explorer FPLC, Amersham Biosciences).

Techniques: Phospho-proteomics, Purification