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Ni-NTA Sanarose 6FF

Ni NTA Sanarose 6FF chelates nickel ions on the high flow rate agarose gel microspheres Sanarose 6FF with triacetic acid as the ligand. The bond and the four valence of metal ions make the chelated metal ions more stable, and has the advantages of withstanding higher reducing agents, good physical and chemical stability, good specificity, and high flow rate.

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Ni-NTA Sanarose 6FF

Ni-IDA Sanarose 6FF

Ni IDA Sanarose 6FF combines the iminodiethyl bond with the trivalent position of bond and metal ion on the high flow rate agarose gel microsphere Sanarose 6FF, with higher load, which is suitable for large-scale production.

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Ni-IDA Sanarose 6FF

AT Protein A Sanarose 4FF

AT Protein A Sanarose 4FF is an affinity medium synthesized by epoxidation of alkali resistant Protein A with a high flow rate agarose substrate. This medium is suitable for capturing monoclonal or Fc fusion proteins from large-scale culture media, as well as polyclonal antibodies from ascites or plasma.

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AT Protein A Sanarose 4FF

Protein G Sanarose 4FF

Protein G Sanarose 4FF is an affinity medium made by immobilizing Protein G onto the Sanarose 4FF substrate through hydrogen bromide activation. Protein G has a wider binding spectrum compared to Protein A, and it not only strongly binds to antibody Fc fragments, but also weakly interacts with antibody Fab fragments. Therefore, Protein G Sanarose 4FF is commonly used for separating and purifying antibodies or antibody fragments from cell culture, as well as purifying antibodies from various species of serum.

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Protein G Sanarose 4FF

Protein A Sanarose 4FF

Protein A Sanarose 4FF is made by coupling the cell wall protein Protein A of Staphylococcus aureus to the agarose gel matrix through epoxy chemical method. It can be widely used in the separation of monoclonal antibodies and polyclonal antibodies. It has the advantages of high load, and the ligand is not easy to fall off. The ligand protein of Protein A Sanarose 4FF has not undergone mutation modification and has limited tolerance to alkali.

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Protein A Sanarose 4FF

IMAC Sanarose 6FF

Metal chelation chromatography medium can independently select chelating metal ions such as Cu ²+、 Zn ²+、 Co ²+ The main principle is that the histidine, cysteine, and tryptophan of proteins can interact with metal ions to achieve separation.

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IMAC Sanarose 6FF

Chelating Sanarose 6FF

Metal chelation chromatography medium can independently select chelating metal ions such as Cu ²+、 Zn ²+、 Co ²+ The main principle is that the histidine, cysteine, and tryptophan of proteins can interact with metal ions to achieve separation.

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Chelating Sanarose 6FF

Blue Sanarose 6FF

Blue Sanarose 6FF, commonly known as blue glue, is an affinity medium that uses Sanarose 6FF as the base and Cibacron Blue F3GA (Cibacron Blue) as the functional ligand. It has the characteristics of physical and chemical stability, difficulty in ligand detachment, long service life, and wide application. Blue Sanarose 6FF has various ways of action and can bind specifically to proteins. It can also be isolated and purified through charge and hydrophobic interactions. This type of medium is widely used for the purification of proteins such as interferon, albumin, and dehydrogenase.

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Blue Sanarose 6FF
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