Cat. No.: HY-K0208

Streptavidin Magnetic Beads

Name: Streptavidin Magnetic Beads
Brand: MedChemExpress
SKU: HY-K0208
Price: 110.00 USD
Availability: InStock
Rating: 5 (226 reviews)

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Based on 226 publication(s) in Google Scholar

MCE Streptavidin Magnetic Beads provide a fast and convenient method for numerous applications, including purification of proteins and nucleic acids, protein interaction studies, immunoprecipitation, immunoassays, pull-down and cell isolation. The 1 mL is defined as the base specification. All larger sizes correspond to incremental volumes of this base.

Storage :
4°C, 2 years. Do not centrifuge, dry or freeze the magnetic beads.

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Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Description & Advantages

MCE Streptavidin Magnetic Beads use recombinant streptavidin covalently coupling to the surface of the paramagnetic beads. Streptavidin, with no carbohydrate group, is different from avidin ensuring low nonspecific binding. The biotinylated molecules (e.g. peptides, proteins, antibodies, sugars, lectins, oligonucleotides, DNA/RNA) bind to the beads due to the high affinity between streptavidin and biotin. MCE Streptavidin Magnetic Beads are removed from the solution manually by using a magnetic stand or automatically by using an instrument.

1. High binding capacity.

2. Low non-specific binding.

3. Minimal sample loss.

4. Ready to use.

Protocol

1. Immobilization Nucleic Acids

1) Resuspend the magnetic beads in the vial (or vortex for 20 seconds), transfer 100 μL of Streptavidin Magnetic Beads into a 1.5 mL tube (transfer amount may be adjusted as required). Place the tube into a magnetic stand to collect the beads against the side of the tube (Hereinafter referred to as magnetic separation). Remove and discard the supernatant.

Note: The amount of beads is sufficient for one reaction. Scale up the reaction as needed.

2) Add 1 mL Wash Buffer I to the beads, invert the tube several times or vortex gently for 15 seconds to mix. Remove and discard the supernatant from magnetic separation. Repeat this step for 2 times.

3) Add 500 μL of biotinylated nucleic acids diluted with Wash Buffer I, makes the beads at a final concentration of 2 mg/mL. Rotate the tube for 30 minutes at room temperature or 2 hours at 4ºC.

4) Separate the biotinylated nucleic acids coated beads with a magnetic stand.

5) Add 1 mL Wash Buffer I to the beads, invert the tube several times or vortex gently for 15 seconds to mix. Remove and discard the supernatant from magnetic separation. Repeat this step for 2 times.

Note: The amount of biotinylated nucleic acids can be calculated by measuring absorbance of the flow through along with absorbance of starting material.

2. Immobilization Antibodies/Proteins

Note: The amount of beads is sufficient for one reaction. Scale up the reaction as needed.

2) Add 1 mL Wash Buffer II to the beads, invert the tube several times or vortex gently for 15 seconds to mix. Remove and discard the supernatant from magnetic separation. Repeat this step for 2 times.

3) Add 1 mL of biotinylated antibodies/proteins with Wash Buffer II, makes the beads at a final concentration of 1 mg/mL. Rotate the tube for 60 minutes at room temperature or 2 hours at 4ºC.

4) Separate the biotinylated antibodies/proteins coated beads with a magnetic stand.

5) Add 1 mL Wash Buffer II to the beads, invert the tube several times or vortex gently for 15 seconds to mix. Remove and discard the supernatant from magnetic separation. Repeat this step for 5 times.

6) Binding is now complete. Resuspend the beads in Buffer II or a buffer suitable for downstream applications to a desired concentration. Use the beads immediately, or store at 4ºC for later use.

3. Elution

3.1 Nucleic acid Elution

Step: Add 50–100 μL of Elution Buffer I to the magnetic beads, incubate for 5 minutes at 65°C or 2 minutes at 90°C, place on a magnetic rack, perform magnetic separation and collect the supernatant.

3.2 Antibody/Protein Elution

a. Denaturation elution: The samples eluted by this method are suitable for SDS–PAGE. Step: Add 50–100 μL of 1 × SDS-PAGE Loading Buffer to the magnetic beads, mix well and heat at 95°C for 5 minutes. Place on a magnetic rack, perform magnetic separation and collect the supernatant.

Note: If you choose denaturation elution, the eluent will contain streptavidin monomers and polymers, biotin-labeled antibody or protein.

b. Non-denaturation elution: The sample eluted by this method retains its original biological activity and can be used for later functional analysis. Step: Add 50–100 μL Elution Buffer II to the magnetic beads and incubate at room temperature for 5-10 minutes. Place on a magnetic rack, perform magnetic separation and collect the supernatant, immediately add 1/10 volume of the total volume of Neutralization Buffer (0.1 M NaOH), adjust the pH of the eluted product to neutral, and the samples is used for later functional analysis.

Note: If you choose non-denaturation elution method, the streptavidin may be dislodged under acidic conditions, and the incubation time should not exceed 10 minutes. Acidic eluents can destroy most of the antibody and antigen interactions, you can wash the beads once with 1mL of 0.1% Tween-20 before elution.