Protein A and Protein G are the gold standard proteins for antibody affinity purification and immunoprecipitation (IP). By covalently coupling both Protein A and Protein G to agarose or magnetic beads, these tools offer a broader binding range compared to beads with only one protein type, enhancing their versatility. Additionally, the Protein A and Protein G used in these products are genetically engineered to retain their high affinity for immunoglobulins (Ig) while eliminating non-primary binding domains, thereby reducing non-specific interactions.

Table 1:Comparison of Protein A/G Agarose Beads and Magnetic Beads

 

rProtein A/G Agarose Resin

Protein A/G MagBeads

Matrix

Highly cross-linked 4% agarose microspheres

Silica-based magnetic beads 

Particle Size

45-165 µm

200 nm

Capacity

>20 mg hIgG/mL resin

>0.7 mg hIgG/mL magnetic beads

Advantages

Easy to use, no auxiliary equipment required

Simple operation

Large pore size, strong binding force

Small diameter, good kinetics

High yield of target protein

Smooth surface, minimal bead adsorption, low background, less antibody consumption

Disadvantages

Porous and prone to adsorption (pre-clear required)

Convenient to use with a magnetic rack

Product Applications

1. Purification of Antibodies

Isolate high-purity antibodies from serum or ascites in a single step.

2. Immunoprecipitation (IP)

Enrich specific proteins to study its characteristics (such as post-translational modifications).

3. Co-Immunoprecipitation (Co-IP)

Enrich target protein to investigate other proteins that bind to it (i.e., protein-protein interactions, protein complexes, etc.).

 

Operation Procedure

Test Data

1. Purification of antibodies from rabbit serum using rProtein A/G Agarose Resin.

Figure 1. Electrophoresis result of antibody purification using rProtein A/G Agarose Resin
 

M: Protein Marker

L: Pre-column crude sample

elu: Elution

  

Figure 1. Electrophoresis result of antibody purification using rProtein A/G Agarose Resin.

2. Antibody Conjugation Experiment with Protein A/G Magbeads

Figure 2. Yeasen Protein A/G Magbeads outperformed Competitor magnetic beads.
 

1: NC

2: Yeasen Protein A/G Magbeads

3: Yeasen Protein A/G Magbeads

4: Competitor

Figure 2. Yeasen Protein A/G Magbeads outperformed Competitor magnetic beads.

3. Use of Protein A/G Magbeads for IP

Figure 3. Yeasen Protein A/G Magbeads outperformed Competitor magnetic beads.

 

 

Target Protein

1: NC

2: Yeasen Protein A/G Magbeads

3: Yeasen Protein A/G Magbeads

4: Competitor

Figure 3. Yeasen Protein A/G Magbeads outperformed Competitor magnetic beads.

4. Use of Protein A/G Magbeads for Co-IP: Specific antibodies against p65 and cyclin-dependent kinase 9 (CDK9) are used for immunoprecipitation analysis of extracted total cellular protein.

Figure 4. Immunoprecipitants were then subjected to western blot analysis using specific antibodies against CDK9 and p65.

Figure 4. Immunoprecipitants were then subjected to western blot analysis using specific antibodies against CDK9 and p65.

  

Product Information

Product Name

Product Number

Specification

Protein A/G Magbeads

36417ES03/05

1 mL/5 mL

rProtein A/G Agarose Resin

36403ES08/25/60

5 mL/25 mL/100 mL

Related Products 

Product Name

Product Number

Specification

SuRi rProtein A Agarose Resin

36401ES08/25/60

5 mL/25 mL/100 mL

rProtein G Agarose Resin

36405ES08/25/60

5 mL/25 mL/100 mL

 

 

 

 

Indagine