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    products/sample-preparation-kits/protein-a-sepharose-column-ab193257.pdf

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Kits/ Lysates/ Other Kits Molecular Biology Kits Beads Protein A
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Protein A Sepharose® Column (ab193257)

  • Datasheet
  • SDS
  • Protocol Booklet
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Key features and details

  • Sample type: Ascites Fluid, Cell culture media, Cell culture supernatant, Serum

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Overview

  • Product name

    Protein A Sepharose® Column
  • Sample type

    Cell culture supernatant, Serum, Cell culture media, Ascites Fluid
  • Product overview

    Contents:
    Ready-to-use pre-packed columns of 1 mL or 5 mL bead volume in PBS with 0.02% sodium azide; >5mg Protein A/mL Sepharose beads.


     


    Features:
    High binding capacity = Binding of IgG ≥16 mg human or rabbit IgG/mL Protein A-Sepharose®.
    Minimal leaching of the ligand
    Flow Rate Tested* = 2.07 mL/min
    *Test condition: = Calculations based on the time required to pass 18 mL of water through 2 mL settled beads (column diameter 1.5 cm).
    Usage = Reusable for up to 10 times without significant loss of binding capacity.


    Store column at 4°C.


    The beads may be damaged above 40°C.


    DO NOT FREEZE.


    Wash beads 3 times with 3x bead volume of desired buffer before use.


     


    Applications:
    - Purification of monoclonal and polyclonal antibodies from culture media, serum, ascites fluid or hybridoma supernatants.
    - Isolation of antibody/antigen complexes in immunoprecipitation experiments, since only the Fc region is involved in antibody binding and the Fab region is available for binding antigen.


     


    Sepharose is a registered trademark of GE Healthcare

  • Notes

    This product is manufactured by BioVision, an Abcam company and was previously called 6508 Protein A Sepharose Column. 6508-5 is the same size as the 5 ml size of ab193257.

    Protein A Sepharose® Columns are prepared by covalently coupling recombinant Protein A to 6% cross-linked Sepharose® beads. Protein A is a genetically engineered protein containing five IgG-binding regions of native Protein A. The cell wall binding region, albumin binding region and other non-specific regions have been eliminated from the recombinant Protein A to ensure maximum specific IgG binding. The coupling technique is optimized to give a higher binding capacity for IgG and minimum leaching of recombinant Protein A. The IgG binding capacity of Protein A Sepharose® Column is ≥ 16 mg human or rabbit IgG per mL of wet beads. Protein A Sepharose® Columns display high chemical and physical stability as well as high flow rate, hydrophilicity and high gel strength. This product can be used for IgG purification and immunoprecipitation.

  • Tested applications

    Suitable for: Purification, IPmore details

Properties

  • Storage instructions

    Store at +4°C. Please refer to protocols.
  • Components 1 ml 5 ml
    Protein A Sepharose® Column 1 x 1ml 1 x 5ml
  • Research areas

    • Kits/ Lysates/ Other
    • Kits
    • Molecular Biology Kits
    • Beads
    • Protein A

Associated products

  • Related Products

    • Bradford Reagent (ab119216)
    • Optiblot SDS-PAGE Sample Preparation Kit (ab133414)
    • Cell Lysis Buffer (ab152163)
    • 10X RIPA Buffer (ab156034)
    • Native lysis Buffer (ab156035)

Applications

The Abpromise guarantee

Our Abpromise guarantee covers the use of ab193257 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
Purification
Use at an assay dependent concentration.

Purification of monoclonal and polyclonal antibodies from culture media, serum, ascites fluid or hybridoma supernatants.

IP
Use at an assay dependent concentration.

Isolation of antibody/antigen complexes in immunoprecipitation experiments, since only the Fc region is involved in antibody binding and the Fab region is available for binding antigen.

Notes
Purification
Use at an assay dependent concentration.

Purification of monoclonal and polyclonal antibodies from culture media, serum, ascites fluid or hybridoma supernatants.

IP
Use at an assay dependent concentration.

Isolation of antibody/antigen complexes in immunoprecipitation experiments, since only the Fc region is involved in antibody binding and the Fab region is available for binding antigen.

Protocols

  • Protocol Booklet

Click here to view the general protocols

Datasheets and documents

  • SDS download

  • Datasheet download

    Download

References (0)

Publishing research using ab193257? Please let us know so that we can cite the reference in this datasheet.

ab193257 has not yet been referenced specifically in any publications.

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