TrueBlot® Anti-山羊 Ig IP Beads 

Upon initial use of this product, we recommend that the vial be inverted several times to get the beads into suspension. We recommend to use a large bore pipet to pipet up the liquid for use. For storage of the opened vial, we recommend that the vial cap be sealed with parafilm to help prevent evaporation of the buffer.

Preparation of Immunoprecipitated Sample for SDS-PAGE:
1. Preclear cell lysate: Add 50 µL of anti-goat IgG beads and 500 µL of cell lysate sample to an eppendorf tube and incubate on ice for
3. minutes. Spin at 10,000xg for 3 minutes and transfer the supernatant to a new eppendorf tube.
2. Immunoprecipitation: Add 5 µg of primary antibody to the eppendorf tube containing the precleared lysate. Incubate on ice for 1 hour. Add 50 µL of Anti-Goat IgG Beads. Incubate for 1 hour on a rocking platform. Spin the eppendorf tube at 10000xg for 1 minute. Remove supernatant completely and wash the (pelleted) beads 3 times with 500 µL of Lysis Buffer.
3. Prepare sample for SDS-PAGE: After the last wash, aspirate supernatant, and add 100 µL Laemmli Buffer (with 50 mM DTT or 2 % ß-mercaptoethanol, final) to bead pellet. Vortex and heat to 90-100 °C for
1. minutes. Spin at 10000xg for 3 minutes, collect supernatant, and load onto the gel. Avoid loading anti-goat Ig beads.
Note: The supernatant can be stored at -20 °C for future use. After thawing, add fresh Reducing Agent (dithiothreitol) and heat as above. Centrifuge the sample at 10000xg for 1 minute in a microcentrifuge to pellet any anti-goat Ig beads and immediately transfer an aliquot of the supernatant to gel wells.

Buffer: 0.01 M Sodium Phosphate, 0.15 M Sodium Chloride, pH 7.2

Stabilizer: None