Agilent 80A StableBond Polypeptide Separation Application Note

This document introduces the separation results of Agilent Technologies' SB-C18, SB-C8, SB-C3, and SB-CN columns at 0-70% B in 36 minutes, and compares them with the separation results on 300Å StableBond columns.


Agilent 80A StableBond Polypeptide Separation Application Note - cover page
Brand
Agilent
Document type
Product Leaflet
Language
English
Pages
2
File format
PDF
File size
124 KB
Published
03 July, 2012
Updated
30 September, 2023
MD5 checksum
5E2B3DD98BAF2BBE9C1CC9BC4850062E

About this manual

This document presents an application for separating various polypeptides, including Angiotensin II, RNase, and the Insulin B chain. The study compares separation results achieved on 80Å StableBond bonded phases against those obtained on 300Å StableBond phases.

The analysis utilizes ZORBAX SB-C18, -C8, -C3, and -CN columns with dimensions of 4.6 x 150 mm. The method employs a mobile phase gradient increasing from 0% to 70% solvent B over 36 minutes, with detection performed via UV at 215 nm.

What's inside

  • Application
  • Highlights
  • Conditions
  • Separation of Polypeptides
  • StableBond Columns

Specifications

Column Dimensions4.6 x 150 mm
Flow Rate1.0 mL/min
Injection Volume10 pl
Detection Wavelength215 nm

Frequently asked questions

Which polypeptides are separated in this application?

The document lists Angiotensin II, RNase, and Insulin B chain as the samples analyzed.

What is the recommended pore size for separating peptides of about 4000 daltons or more?

Peptides of this molecular weight should be separated on a wide-pore column.

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