SKU: 186008987
XBridge Peptide BEH C18 XP Column, 130Å, 2.5 µm, 4.6 mm X 150 mm, 1/pk

XBridge Peptide BEH C18 XP Column | 186008987


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Product Description

The XBridge Peptide BEH C18 XP Column, 130Å, 2.5 µm, 4.6 mm X 150 mm columns are optimized and QC tested for peptide separations. The small-pore (130Å) trifunctionally bonded BEH particle offers the widest usable pH range, superior low pH stability, and ultra-low column bleed for proteomic, peptide mapping, and synthetic peptide applications. Each batch is specifically QC tested using a gradient separation of a tryptic digest of cytochrome c (p/n: 186006371) to before being QC accepted as a Peptide separation column.

Suggested Use: Peptide Separations, Peptide Analysis

Specifications

  • Chemistry

    C18

  • Separation Mode

    Reversed Phase

  • Temperature Limits

    90 C

  • Maximum Pressure

    10000 psi (689 Bar)

  • Particle Size

    2.5 µm

  • Pore Size

    130 Å

  • QC Tested

    Peptide

  • Format

    Column

  • System

    HPLC, UHPLC

  • Particle Technology

    BEH

  • USP Classification

    L1

  • Inner Diameter

    4.6 mm

  • Length

    150 mm

  • 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 XP Column, 130Å, 2.5 µm, 4.6 mm X 150 mm, 1/pk

Utilize the XBridge Peptide BEH C18 XP Column to analyze samples for proteomics with the widest usable pH range at low pH stability and ultra-low column bleed. The lab equipment also supports protein characterization and peptide synthesis using the trifunctionally bound BEH particle. Peptide separations are adjusted and quality-controlled evaluated for using the XBridge BEH C18 Peptide Separation Technology (PST) columns.

Benefit from the analytical column's Protein Separation Technology, which integrates BEH technology and uses synthetic particles that deliver the best quality along with consistent performance, by adding the XBridge Peptide BEH C18 XP Column to your collection of lab equipment.

To ensure that peptide separation techniques are stable, the XBridge Peptide BEH C18 XP Column is quality-controlled and evaluated using a peptide map. This is made achievable by employing well-studied, cutting-edge bonding techniques for the C18 ligand, which give predictable behavior with the range of samples utilized in proteomics, protein characterization, and peptide synthesis. You may rely on the analytical column's dependability as a result, and you will receive reliable batch-to-batch separations of synthetic peptides and protein digests. The processes utilized to make the lab equipment guarantee stable particle structure and bonding chemistry across a wide pH range and at high temperatures.

The packing materials for the XBridge Peptide BEH C18 columns are produced in a cGMP, ISO 9002 certified facility using an ultra-pure reagent and have been engineered to give good peak shape, high efficiency, and outstanding stability. Every batch of XBridge Peptide BEH C18 Column material is qualified with a peptide separation, and the outcomes are held to predefined tolerance limits. To ensure great, repeatable performance for peptide separations, this is done. Each column is packaged with a Performance Test Chromatogram and a Certification of Acceptance and undergoes extensive testing before being shipped out.

Protect your analytical column from harm by using the XBridge Peptide BEH C18 VanGuard Cartridge, 130Å, 2.5 µm, 3.9 mm X 5 mm, 3/pk alongside the column. The cartridge is made using the exact same materials that are present in the column, making the two lab equipment ideally suited. The cartridge prevents the entry of unwanted pollutants into the mobile stream, ensuring that the analysis results you receive are more accurate and reliable. The use of the cartridge also makes sure that the column lasts a long time.

Why Is Protein Separation Crucial?

The characterization of the function, structure, and interactions of the target protein depends on its purification. The process of purification may first separate the mixture's protein and non-protein components before separating the desired protein from all other proteins.