Immunoglobulin (Ig) is a kind of globulin with antibody activity and specific binding reaction with corresponding antigen. It is a kind of protein produced by lymphocytes in vertebrate immune response to antigenic stimulation and generally exists in mammalian blood, tissue fluid, lymph and in vitro secretion. With the development and demand of immunology, the purification of immunoglobulins and their components has become an essential means. Below, we will introduce several commonly used methods for purifying immunoglobulins.


1、 Salting out method

Salt precipitation, as an important precipitation method, is often used in the laboratory to separate and purify proteins, especially for the preliminary separation of raw materials. The solubility of proteins in water depends on the degree of hydration of protein molecules. Adding inorganic salts to change the degree of hydration of proteins can cause protein precipitation. Due to the different number and distribution of polar groups on the surface of various proteins, as the amount of inorganic salts added increases, the precipitation order of different proteins varies. Therefore, by controlling the amount of inorganic salts added, protein separation and purification can be achieved through graded precipitation.


2、 Ion exchange chromatography

Ion exchange refers to the reversible exchange reaction between ions in the liquid phase and dissociative groups on the stationary phase. Using this reaction, the mixture to be separated is first dissociated in a solution of a certain pH, and then flows through the stationary phase to exchange ions with the dissociatable groups on the stationary phase, adsorbing them onto the stationary phase. Any components that cannot be exchanged or adsorbed are then discharged from the chromatographic column. Based on the differences in the dissociation degrees of each group adsorbed on the fixed phase through exchange, solutions with different pH values or salt concentrations are used as mobile phases. Each component is then exchanged and eluted through a chromatography column, and the mixture components are separated to achieve separation. This is called ion exchange chromatography.


3、 Gel filtration method

Gel particles are a network structure. When mixtures with different molecular sizes pass through the gel column, the larger molecules come down first, and the smaller molecules are embedded in the network structure of gel particles and then come down, so as to separate substances with different molecular sizes, which is the role of molecular sieves. Common gel: dextran gel, polyacrylamide gel, agarose gel, and G150 is commonly used to separate Ig.


4、 Affinity chromatography

By utilizing the specificity and reversibility of antigen antibody binding, the purified antigen is first cross-linked onto the carrier (agarose beads) to create an affinity chromatography column. When Ab (Ig) passes through, it binds specifically to the antigen on the column, and impurities in Ab flow out. Then, Ab is released by changing the buffer pH and ionic strength.


 Bona Biotechnology focuses on providing overall solutions for separation and purification projects for domestic and foreign customers, and has become a major research and development and production enterprise and supplier of liquid phase fillers and membrane separation and purification equipment in China. It has reached an advanced level in the development and application of separation and purification technology. If you encounter difficulties in separation and purification, please feel free to contact us at any time, and we will have professional technical personnel to answer your questions.



Shandong Bona Biotechnology Group Co., Ltd. has utilized its professional advantages in membrane separation technology for many years, and after repeated experiments and demonstrations, has successfully developed and produced a plasma protein membrane concentration process. Not only does it reduce the production cost of plasma protein powder, but it also reduces the ash content of plasma protein powder and improves the quality of the product.


Membrane concentration process for plasma protein:

Plasma storage tank → Pretreatment system → Ultrafiltration membrane feed pump → Ultrafiltration membrane filtration system → Ultrafiltration membrane high-pressure circulation pump → Ultrafiltration membrane concentration and separation system → Concentrated plasma storage tank


1、 Design basis

Select a certain molecular weight ultrafiltration membrane and use a unique technology to concentrate and separate the plasma separated by a high-speed tube centrifuge, removing some moisture and ash. This concentration system is designed with continuous feeding and discharging, which is filtered by the pre-treatment system before entering the membrane system. The plasma is transported by the feed pump to the filtration system configured by the ultrafiltration membrane itself, and then enters the high-pressure pump. The plasma concentration is achieved through the pressure increase of the high-pressure pump. The concentrated plasma is sent to the product refrigeration circulation tank for subsequent treatment, and the concentrated effluent is directly discharged.


2、 Design basis

This technology belongs to the field of ultrafiltration membrane concentration material treatment, involving the optimization of traditional plasma membrane treatment processes and the improvement of membrane efficiency and service life. Fresh plasma has undergone excellent anticoagulation pretreatment to ensure that there are no flocculent substances in the plasma before entering the membrane system; Fresh blood that has undergone anticoagulation treatment and refrigerated transportation at the slaughterhouse must be separated from plasma and blood cells at the ultrafiltration membrane concentration site using a high-speed tube centrifuge; The color of the separated plasma is relatively light.


Technical advantages of plasma protein membrane concentration process:

1. The membrane concentration process is room temperature concentration, and there is no phase change during the concentration process. Under the same conditions, the concentration energy consumption is much lower;

2. The membrane concentration process is concentrated at room temperature, which can prevent the denaturation and inactivation of thermosensitive proteins while effectively preventing plasma from freezing at high temperatures;

3. During membrane concentration, some inorganic salts are removed, reducing ash content and effectively improving product quality;

4. The membrane concentration system adopts a cross flow process, which can effectively solve the problem of membrane fouling and blockage;

5. Membrane equipment occupies a small area, has a long service life, and reduces production costs and investment;

6. High degree of automation, clean production, reduced labor intensity, safe and reliable.



Team A
Team B
Team C

Can you introduce your product

How do you charge for it?

Do you have any discounts?

请您留言

Shandong Bona Biotechnology Group Co., Ltd Consultation hotline: 0531-88804339

提交