4374321
iTRAQ® Reagent Application Kit - Protein
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About This Item
Productos recomendados
shipped in
dry ice
storage temp.
−20°C
General description
Contains sufficient reaction solutions, test mixture and iTRAQ® Reagents 114, 115, 116 and 117 (for 25 μg protein) to label 10 duplex, 6 three-plex or 5 four-plex experiments.
Application
This iTRAQ application kit for protein provides iTRAQ reagents and protocol to label protein prior to digestion. This iChemistry kit can be used in workflows that include SDS-PAGE separation and in-gel protein digestion, followed by LC/MS/MS analysis. Trypsin is sold separately.
Analysis Note
To view the Protocol for the iTRAQ Reagents 4-plex Application Kit - Protein, please visit this Protocol link.
To view the Chemistry Quick Reference Card for the iTRAQ Reagents, please visit this Chemistry Quick Reference Card link.
To view the Chemistry Quick Reference Card for the iTRAQ Reagents, please visit this Chemistry Quick Reference Card link.
Legal Information
iTraq is a registered trademark of AB Sciex Pte. Ltd.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2
Storage Class
3 - Flammable liquids
flash_point_f
35.6 °F - closed cup
flash_point_c
2.0 °C - closed cup
Certificados de análisis (COA)
Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»
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Nature protocols, 6(10), 1578-1611 (2011-10-01)
Analysis of the sequence and nature of protein N termini has many applications. Defining the termini of proteins for proteome annotation in the Human Proteome Project is of increasing importance. Terminomics analysis of protease cleavage sites in degradomics for substrate
Cell cycle (Georgetown, Tex.), 11(12), 2367-2379 (2012-06-08)
Cisplatin chemoresistance is a clinical problem that leads to treatment failure in various human epithelial cancers. Members of tumor protein (TP) p53 family play various critical roles in the multiple molecular mechanisms underlying the chemoresistance of tumor cells. However, the
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