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Your Position: 홈 > Beads > B7-H3 > MBS-K040

Human B7-H3(4Ig)-coupled Magnetic Beads

ItemsSize （2mg）Size（5mg X 2）
Particle size2 μm2 μm
Physical appearancePowder mixturePowder mixture
Amount of Coupled Protein≈1988 pmol (100 μg) Human B7-H3(4Ig)/mg beads≈1988 pmol (100 μg) Human B7-H3(4Ig)/mg beads
Binding Capacity>596 pmol (30μg) Anti-B7-H3 Ab/mg beads>596 pmol (30μg) Anti-B7-H3 Ab/mg beads
FormulationPBS, pH7.4, with 10% TrehalosePBS, pH7.4, with 10% Trehalose
Reconstitution2 mL sterile deionized water (1 mg beads/mL)5 mL sterile deionized water (1 mg beads/mL)
  • Background
    The Human B7-H3-coupled Magnetic Beads is produced by coupling biotinylated human B7-H3 protein to streptavidin-conjugated magnetic beads. The pre-coupled beads are ready to use for capturing anti-B7-H3 antibody from your sample with high specificity.
  • Source
    Human B7-H3 Protein is expressed from human 293 cells (HEK293). It contains AA Gly 27 - Thr 461(Accession # Q5ZPR3-1).
  • Application
    This product is intended for immunocapture, biopanning and flow cytometry. This product is produced non-sterile.
    *The Isotype control (Cat. No. SMB-B01) is sold separately.
  • Reconstitution

    See Certificate of Analysis (CoA) for detailed instruction.

  • Storage
    Upon receipt, please store the beads at -20°C for 1 year in lyophilized state. Please avoid more than 3 freeze-thaw cycles once reconstitution, immediate use after reconstitution is highly recommended.
  • Assay Principles
    Antibody Purification: 1. Reconstitute the beads with ultrapure water to 1 mg/mL, and wash the beads for three times. 2. Dilute the biotinalyted protein or antibodies with Assay Buffer and add to the beads. Incubate for 60 minutes at room temperature in a rotary mixer. 3. Wash the beads for four times, and add Assay Buffer to the beads. The beads are ready to use for the next experiment.

    The magnetic beads technology makes use of the easy and efficient collection of beads in magnetic field to facilitate antibody purification in a simple workflow of “bind-wash-elute”. In contrast to common separation techniques, this method does not require columns or centrifugation, and is therefore ideal in high-throughput applications.

  • Formulation

    Please contact us for detailed information.

    Contact us for customized product form or formulation.

Typical Data
B7-H3 TYPICAL DATA

Immobilized 22.7 μg B7-H3(4Ig) to 1mg Beads can bind the Anti B7H3 Ab with an EC50 of 1.039 μg/mL.

Protocol
  • Clinical and Translational Updates

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