Protein A/G Magnetic Beads

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Product Details

Summary
Product Discontinued
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Order Details


    • Catalog Number
      NBP1-71715
    • Availability
      Product Discontinued

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Datasheet
Reviews & Publications
Protocols & FAQs
Support & Research

Applications/Dilutions

Dilutions
  • Chromatin Immunoprecipitation
  • Immunoprecipitation
  • Western Blot
Application Notes
Protein AG Magnetic Beads are useful for Immunoprecipitation for analysis in non-reducing conditions as well as Antibody Purification. Sufficient For: Binding 55 to 85 ug rabbit IgG/mg beads. Also useful in Chromatin Immunoprecipitation. Beads are 1um in diameter.
Publications
Read Publication using NBP1-71715.

Packaging, Storage & Formulations

Storage
Store at 4C. Do not freeze.
Buffer
supplied at 10mg/mL in water containing 0.05% NaN3
Concentration
Please see the protocols for proper use of this product. If no protocol is available, contact technical services for assistance.

Notes

Important Product Information: Do not centrifuge, allow beads to dry or freeze. Centrifuging, drying or freezing will cause the beads to aggregate and lose binding activity. Always vortex beads to fully resuspend before pipetting. To minimize protein degradation, include protease inhibitors in preparation of cell lysates. - A low-pH elution may be used for single-use applications. Optimal time for low-pH elution is 10 minutes; exceeding 10 minutes may result in nonspecific binding and yield reduction. - When using rabbit antibodies (primary or secondary) in downstream Western blot applications, perform elution in SDS-PAGE sample buffer at room temperature. For all other antibody species, boiling the beads in SDS-PAGE sample buffer is acceptable for single-use applications. Boiling could cause bead aggregation and loss of binding activity. Protein A/G Magnetic Beads are compatible with small-scale antibody purification and immunoprecipitation and analyses by Western blot and mass spectrometry. Protein A/G has a broader binding range than either Protein A or Protein G individually. Protein A/G binds to all human IgG subclasses, binds somewhat to IgA, IgE, IgM and, to a lesser extent, IgD. Unlike Protein G, Protein A/G does not bind serum albumin because the gene sequence coding for the albumin-binding site has been eliminated. Protein A/G is effective for mouse monoclonal antibody purification from IgG subclasses because Protein A/G binds all mouse IgG subclasses but does not bind murine IgA, IgM or serum albumin.

Background

The recombinant Protein A/G that is immobilized onto the Magnetic Beads is a fusion of the IgG binding domains of both Protein A and Protein G. Protein A/G contains four Fc-binding domains from Protein A and two from Protein G, making it a convenient tool for investigating and purifying immunoglobulins. Thus, Magnetic Particles are not simply a mixed immobilization of separate Protein A and Protein G polypeptides, nor are they a mixture of Protein A magnetic beads and Protein G magnetic beads.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Support products are guaranteed for 6 months from date of receipt.

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