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ACQUITY Premier Glycoprotein BEH Amide, 300 Å, 1.7 µm, 2.1 x 20 mm Column, 1/pk
Part Number:
186011017
Manufacturer:
Waters
€965.00
%
Delivery Time:
approx. 5 days (product only available in Germany)
Excl. 19% taxes, excl.
Shipping costs
Packaging unit:
1 Stk.,
Minimum order quantity:
1 pc
Request a quote
Product Description
ACQUITY Premier Glycoprotein BEH Amide, 300 Å, 1.7 µm, 2.1 x 20 mm Column, 1/pk
Product details
| Description | ACQUITY Premier Glycoprotein BEH Amide, 300 Å, 1.7 µm, 2.1 x 20 mm Column, 1/pk |
|---|---|
| Quantity | 1 Stk. |
| Manufacturer | Waters |
| Brand | ACQUITY |
| Product Type | HPLC Column |
| Length | 20 mm |
| Internal Diameter | 2.1 mm |
| Particle Size | 1.7 µm |
| Chemistry | Amide |
| Chemistry Producers Term | Premier Glycoprotein BEH Amide |
| Pore Size | 300 Å |
| USP Class | L68 |
| Carbon Load | 12.0 % |
| Bet Surface Area [m2/g] | 185.0 |
| Endcapping | non endcapped |
| Country of Origin | United States of America (USA) |
| Column Type | Analytical Column |
| Hardware Material | Inert Stainless Steel |
| Hardware Type | Ready-to-use Column |
| pH Minimum | 2.0 |
| pH Maximum | 10.0 |
| Technology | U(H)PLC |
| Matrix | Hybrid |
| Particle Morphology | spherical, fully porous |
| Pressure Stability | 1034 bar |
Support-Downloads
Applications Notes Guides
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Waters Analysis of Glycopeptide Glycoforms in Monoclonal Antibody Tryptic Digest using a UPLC HILIC Column
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Waters Analysis of N-Linked Glycans from Coagulation Factor IX, Recombinant and Plasma Derived, Using HILIC UPLC/FLR/QTof MS
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Waters Characterization of EPO N-Glycans using RapiFluor-MS and HILIC Profiling
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Waters MaxPeak High Performance Surfaces Technology Improves HILIC Profiling of Released N-Glycans
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Waters N-Linked Glycans of Glycoproteins: A New Column for Improved Resolution
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Waters Quality Control and Automation Friendly GlycoWorks RapiFluor-MS N-Glycan Sample Preparation
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Waters Rapidly Monitoring Released N-Glycan Profiles During Process Development Using Rapi Fluor-MS and the ACQUITY QDa Detector : Waters
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Waters UPLC Separation of 2-AB Labeled Fetuin Glycans Removed by Exoglycosidase
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Waters Comprehensive Characterization of the N and O-Linked Glycosylation of a Recombinant Human EPO
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Waters Enhancing the Peak Capacity of High Molecular Weight N-Glycan HILIC Separations with a Wide-Pore Amide Bonded Stationary Phase
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Waters Developing High Resolution HILIC Separations of Intact Glycosylated Proteins Using a Wide-Pore Amide-Bonded Stationary Phase
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Waters Acquity Glycoprotein Beh Amide Hilic Glycopeptide Mapping Uhplc Applications
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Waters Mapping IgG Subunit Glycoforms Using HILIC and a Wide-Pore Amide Stationary Phase
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Waters Measuring the Glycan Occupancy of Intact mAbs using HILIC and Detection by Intrinsic Fluorescence
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Waters Acquity Glycoprotein Beh Amide Optimizing Hilic Based Analyses Rapifluor Ms Labeled Sialylated N Glycans Uhplc Applilcations
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Waters Increased Resolving Power for Acidic Glycans with an MS-Compatible Anion Exchange Reversed Phase Separation
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Waters Glycan Application Notes Sample Preparation Hplc Uhplc Applilcations
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Waters DMB-Labeled Sialic Acid Analyses Using HPLC-, UHPLC-, and UPLC-Based, BEH C18 Columns