Human VEGF165-coupled Magnetic Beads

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MBS-K036-2mg
$950.00
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MBS-K036-10mg (5mg X 2)
$2,960.00
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MBS-K036
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Product Information
Items
Size 2mg
Size 10mg (5mg × 2)
Particle size
2 μm
2 μm
Physical appearance
Powder mixture
Powder mixture
Binding Capacity
>137 pmol (20μg) Anti-VEGF antibody/mg beads
>137 pmol (20 μg) Anti-VEGF antibody/mg beads
Formulation
PBS, pH7.4, with 10% Trehalose
PBS, pH7.4, with 10% Trehalose
Reconstitution
2 mL sterile deionized water (1 mg beads/mL)
5 mL sterile deionized water (1 mg beads/mL)
Product Description

The Human VEGF165-coupled Magnetic Beads is produced by coupling biotinylated human VEGF165 protein to streptavidin-conjugated magnetic beads. The pre-coupled beads are ready to use for capturing anti-VEGF165 antibody or VEGFR2/KDR protein from your sample with high specificity. The uniform size and large surface-to-volume ratio of the beads ensure highly efficent immunocapture in a simple, fast and convenient workflow with high reproducibilty of data.

Application

This product is intended for immunocapture, biopanning. This is a non-sterile product.

* 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. The shelf life is 1 year at -20 °C.

Please avoid more than 3 freeze-thaw cycles once reconstitution, immediate use after reconstitution is highly recommended.

Assay Principles

Antibody Purification:
1. Resuspend the lyophilized beads by adding the buffer of choice.
2. Add analyte to the suspension, mix and incubate to enable specific binding of the beads and the target protein.
3. Magnetize beads, remove supernatant, and wash unbound protein fractions to capture target protein-bound beads.
4. Wash, magnetize the beads and collect purified target protein for use in downstream applications.

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.