TT0010
Trypsin-Spinsäulen
for proteomics
Synonym(e):
Immobilized TPCK- treated Trypsin, Immobilized Trypsin
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About This Item
UNSPSC-Code:
12352200
NACRES:
NA.56
Empfohlene Produkte
Qualität
for proteomics
Lagertemp.
2-8°C
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Allgemeine Beschreibung
Enjoy all of the advantages of Proteomics Grade Trypsin in a 15-minute digestion. A staple of mass spec sample preparation, efficient tryptic digestion is essential to successful proteomic analyses. While traditional digests require up to 18 hours, the same digest can be accomplished in only 15 minutes using the Trypsin Spin Column, Proteomics Grade.
This ultra-micro spin column contains highly purified, TPCK-treated porcine trypsin immobilized on a spherical 20 micron silica support, chemically modified to minimize non-specific adsorption. Eluted peptides are ready for MS analysis, and require no additional clean-up. Ideal for rapid protein digestion of small volumes (100 μl or less), the Trypsin Spin Column is a New Spin on MS Sample Prep!
This ultra-micro spin column contains highly purified, TPCK-treated porcine trypsin immobilized on a spherical 20 micron silica support, chemically modified to minimize non-specific adsorption. Eluted peptides are ready for MS analysis, and require no additional clean-up. Ideal for rapid protein digestion of small volumes (100 μl or less), the Trypsin Spin Column is a New Spin on MS Sample Prep!
Leistungsmerkmale und Vorteile
Entdecken Sie die Vorteile für sich selbst!
- 15 Minuten Verdau
- Ideal für 10 bis 100 μg Proteinproben
- Minimale chymotryptische Aktivität
- Keine zusätzliche Aufreinigung erforderlich
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Produkt-Nr.
Beschreibung
Preisangaben
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral
Lagerklassenschlüssel
10 - Combustible liquids
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Shama P Mirza et al.
Journal of proteome research, 7(7), 3042-3048 (2008-05-31)
Proteomics-based quantification methods for differential protein expression measurements are among the most important and challenging techniques in the field of mass spectrometry. Though numerous quantification methods have been established, no method meets all the demands for measuring accurate protein expression
Jiangjiang Liu et al.
Journal of the American Society for Mass Spectrometry, 20(5), 819-828 (2009-02-10)
This work uses electrospray ionization mass spectrometry (ESI-MS) in conjunction with hydrogen/deuterium exchange (HDX) and optical spectroscopy for characterizing the solution-phase properties of cytochrome c (cyt c) after heat exposure. Previous work demonstrated that heating results in irreversible denaturation for
Tomoharu Takeuchi et al.
Biological & pharmaceutical bulletin, 34(7), 1139-1142 (2011-07-02)
To study the endogenous counterpart of LEC-6, a major galectin in Caenorhabditis elegans, the proteomic analysis of glycoproteins captured by an immobilized LEC-6 column was performed using the nano liquid chromatography-tandem mass spectrometry (LC-MS/MS) technique. A protein recovered in a
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