Ig

Contents: TrueBlot™ anti-Goat Ig IP Beads
Catalog Number: 00-8844
Formulation: Phosphate buffer pH 7.2,
150 mM NaCl, 0.09% NaN₃
Storage Conditions: Store at 4°C.
DO NOT FREEZE.

Prices for This Product*
Cat. No.	Size	Price	Qty	Action
00-8844-25	2.5 ml	$170

*International customers: Please contact your distributor for region specific pricing.

Available Formats of This Product
Cat. No.	Format	Excite (nm)	Emit (nm)	Reported Applications
00-8844	TrueBlot™ anti-Goat Ig IP Beads (Binds 1.0mg Ig/ml beads)	N/A	N/A	IP

Questions? Please consult our answers to frequently asked questions at http://www.ebioscience.com/faq.

Description

TrueBlot^TM anti-Goat Ig IP Beads are a suspension of activated agarose beads coupled with rabbit anti-goat IgG. It is suitable for precipitation of goat IgGs used as the primary antibodies in immunoprecipitation assays. The beads are in suspension and will settle upon storage. Prior to use, mix the vial gently (do not vortex) to ensure delivery of proper bead volume.

Applications Reported

For research use only, not for diagnostic or therapeutic use. TrueBlot^TM anti-Goat Ig IP Beads (binds 1 mg Ig/ml beads) have been reported for use in immunoprecipitation.

Applications Tested

TrueBlot™ anti-Goat Ig IP Beads have been tested by immunoprecipitation and immunoblotting detection using Goat TrueBlot™ (cat# 18-8814).

Procedure: 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 30 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% β-mercaptoethanol, final) or NuPAGE LDS Sample Buffer (Invitrogen Cat#NP0007) containing NuPAGE Sample Reducing Agent (dithiothreitol; Invitrogen Cat#NP0004) to bead pellet. Vortex and heat to 90-100°C for 10 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 NuPAGE Sample 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.

Special Notes

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.

Related Products

Cat. 18-8814 Goat TrueBlot™: Horseradish Peroxidase (HRP) anti-goat IgG