AC050-003 AbSelect Serum Antibody Purification System (3 Purifications, each up to 20mg IgG)

Search for all "AbSelect Serum Antibody Purification System"


More Views

  • AC050-003

Properties for AbSelect Serum Antibody Purification System

Product Category Labeling Kits & Reagents
Quantity 1 set
Reaction 3 Purifications, each up to 20mg IgG
Shipping to Worldwide
PDF datasheet View Datasheet
Manufacturer Acris Antibodies GmbH

Datasheet Extract

Background Antibodies generated from Ascites fluid and Serum are often supplied as crude formulations. Both Ascites fluid and Serum contain many substances that interfere with antibody labeling reactions. Successful labeling therefore requires antibodies to be purified prior to labeling. The AbSelect Serum system AC050 is a fast and simple method to purify antibodies from these types of media.

AbSelect Serum is prepared by coupling highly purified Protein A to Agarose beads which can be used to purify IgG fractions from Ascites fluid and Serum. The method involves the capture of the antibody on the AbSelect Serum Resin and the removal of unwanted substances using a simple wash procedure. The purified product is then eluted and neutralized.

The components of the AbSelect Serum purification system are fully compatible with the Link-A-Light antibody labeling kits (available separately), which allows the purified antibody to be immediately labeled with an enzyme, fluorescent protein or fluorescent dye, with a hands-on time of under 30 seconds.
Protocols 1. Amount of antibody that can be purified
Up to 20 mg of antibody can be purified in each run. The volume of sample required will depend on the host species (See Appendix 2).

2. Preparing the Serum or Ascites Fluid
Add the 10x Binding Buffer AC050-003-B to the Serum or Ascites fluid. The volume to add is 1/10 of the volume of the sample. For example, for 5 ml of Serum add 0.5 ml of 10x Binding Buffer AC050-003-B. Mix by inversion. Note: For sample volumes of less than 5 ml, dilute the sample with Wash Buffer AC050-003-W to 5 ml before adding the 10x Binding Buffer AC050-003-B.

3. Incubation of Sample with Resin
Add the AbSelect Resin AC050-003-R to the Serum and incubate with mixing at room temperature for a minimum of 2 hours. Use the Supernatant to rinse the bottle to recover all AbSelect Resin.

4. Packing of the Column
Carefully pour the Sample-Resin mix into the column. Sample volumes of more than 10 ml will have to be added in aliquots. The AbSelect Serum Resin will collect in the bottom of the column.
The unwanted supernatant will pass through the column and can be kept on ice until a successful outcome has been confirmed.

5. Wash Procedure
Wash the column with 7 ml of Wash Buffer AC050-003-W to remove any non-bound protein.
Repeat the wash procedure three times.
Note: Wash the inner surface of the column to remove any residual starting material.

6. Elution
The antibody is eluted in 1 ml fractions.
Place a collecting tube under the column and add 1 ml of Elution Buffer AC050-003-E (See Section 8).
Remove the collection tube and add 0.25 ml of Neutralization Buffer AC050-003-N.
Cap the tube and place to one side.
Repeat the elution process three more times, each time neutralizing the sample as it is eluted.
The Neutralizing Buffer AC050-003-N must be added as soon as possible to avoid prolonged exposure to low pH which can result in denaturation of the IgG.
The protein normally elutes in tubes 1 and 2 but you should confirm this using a Test for protein (Section 8) before pooling any of the tubes.

7. Antibody Concentration (Optional)
If the concentration of the recovered antibody is low then it can very quickly and easily be concentrated using our Antibody Concentration and Clean Up Kit (Cat.-N AC048 available separately).

8. Test for Protein
Wherever possible protein values should be determined using absorbance at 280nm.

When other methods of are used such as BCA or Bradford protein assays, determinations should be performed before the addition of the Neutralization Buffer AC050-003-N, as this can interfere with these reagents. Remove an aliquot for protein determination and neutralize the rest of the fraction immediately as the low pH of the elution buffer can denature the antibody.

When using Bradford-type reagents it is important to use an IgG standard curve. Failure to do this will result in incorrect protein levels being calculated. If IgG is not available then a BSA standard curve can be used, but the IgG levels will be under-estimated by a factor of 2.3.
Storage Storage of Kit: The kit is shipped at ambient temperature. Store the kit at 4°C upon receipt.

Storage of Antibody: Store at 4°C. Other storage conditions (e.g. frozen at -70°C) may also be satisfactory. The sensitivity of any particular antibody to freeze- thaw should be determined by experimentation on small aliquots
  • LinkedIn