SKU: 186003625
XBridge Peptide BEH C18 Column, 300Å, 5 µm, 4.6 mm X 250 mm, 1K - 15K, 1/pk

XBridge Peptide BEH C18 Column | 186003625


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Product Description

The XBridge BEH300 C18 Peptide Separation Technology (PST) columns are optimized and QC tested for peptide separations. The wide-pore (300Å) trifunctionally bonded BEH particle offers you the widest usable pH range, superior low pH stability, and ultra-low column bleed to assay samples for proteomics, protein characterization, and peptide synthesis.

Specifications

  • Chemistry

    C18

  • Separation Mode

    Reversed Phase

  • Particle Substrate

    Hybrid

  • pH Range Min

    1 pH

  • pH Range Max

    12 pH

  • Maximum Pressure

    6000 psi (415 Bar)

  • Endcapped

    Yes

  • Silanol Activity

    Low

  • Molecular Weight Range Min

    1000

  • Molecular Weight Range Max

    15000

  • Particle Shape

    Spherical

  • Particle Size

    5 µm

  • Endfitting Type

    Waters

  • Pore Size

    300 Å

  • QC Tested

    Peptide

  • Format

    Column

  • Surface Area

    185

  • System

    HPLC

  • Particle Technology

    BEH

  • USP Classification

    L1

  • Inner Diameter

    4.6 mm

  • Length

    250 mm

  • Carbon Load

    18 %

  • UNSPSC

    41115709

  • Application

    Peptide

  • Brand

    XBridge

  • Product Type

    Columns

  • Units per Package

    1 pk

Product Support

Documents

Documents



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XBridge Peptide BEH C18 Column, 300Å, 5 µm, 4.6 mm X 250 mm, 1K - 15K, 1/pk

Use the XBridge Peptide BEH C18 Column to get the widest usable pH range at low pH stability and ultra-low column bleed to assay samples for proteomics. The wide-pore (300Å) trifunctionally bonded BEH particles of the lab equipment also give you access to protein characterization and peptide synthesis. The XBridge BEH300 C18 Peptide Separation Technology (PST) columns are optimized and QC tested for peptide separations.

Invest in the XBridge Peptide BEH C18 Column and add it to your lab equipment assortment so you can take advantage of the analytical column’s Protein Separation Technology which incorporates BEH technology and uses synthetic particles that offer the highest quality combined with consistent performance.

To ensure the stability of peptide separation methods, the XBridge Peptide BEH C18 Column is QC tested with a peptide map. This is achieved by the use of well-characterized, state-of-the-art bonding procedures for the C18 ligand present in the analytical column. It also delivers predictable behavior with the variety of samples that are used in proteomics, protein characterization, and peptide synthesis. Consequently, you can depend on the reliability of the analytical column and get consistent batch-to-batch synthetic peptide and protein digest separations. In addition to this, the techniques used for the manufacturing of the lab equipment ensure stable particle structure and bonding chemistry from pH 1 to 12 and at elevated temperatures.

The XBridge Peptide BEH C18 column uses packing materials that have been designed to provide excellent peak shape, high efficiency, and excellent stability and are manufactured in a cGMP, ISO 9002 certified plant using ultra-pure reagents. Each batch of XBridge Peptide BEH C18 Column material is qualified with a peptide separation, and the results are held to narrow specification ranges. This is done to guarantee excellent, reproducible performance for peptide separations. Every column is tested and a Performance Test Chromatogram, along with a Certification of Acceptance, are included in the packaging with each column, so you are certain of the quality of the products you receive.

Shop for lab equipment by browsing through our catalog. You may also want to read further about the LCGC Certified Clear Glass 12 x 32 mm Screw Neck Vial, with Cap and Preslit PTFE/Silicone Septum, 2 mL Volume, 100/pk.

Why Must Proteins And Peptides Be Purified Prior To Analysis?

Protein and peptide purification is vital for the specification of the function, structure, and interactions of the protein of interest. The purification process may separate the protein and non-protein parts of the mixture and finally, separate the desired protein from all other proteins.