Anti-DYKDDDDK affinity agarose is made by covalent coupling of high-quality DYKDDDDK mouse monoclonal antibody and agarose gel. It has the characteristics of high binding capacity of protein, high specificity, stability and repeatability. It can be used for affinity purification and immuno (co) precipitation of DYKDDDDK tagged fusion proteins.
Anti-DYKDDDDK immunomagnetic beads is made by covalently coupling high-quality DYKDDDDK mouse monoclonal antibody and magnetic beads, It has characteristics of high binding capacity of protein, high specificity, fast and convenient operation, stability and repeatability. It can be used for affinity purification and immuno (co) precipitation of DKKDDDDK tagged fusion proteins.
Anti-DYKDDDDK-tag fast IP kit is composed of Anti-DYKDDDDK affinity gel, Mouse IgG affinity gel, DYKDDDDK-Tag Rabbit pAb and Goat Anti-Rabbit IgG(peroxidase/HRP conjugated), which is used for fast, efficient and specific (Co)IP of DYKDDDDK tag fusion protein.Anti-DYKDDDDK affinity gel is made by covalent coupling of high-quality DYKDDDDK-Tag Mouse mAb and Sepharose 4B agarose granules. It has the characteristics of high binding capacity of protein, high specificity and stability. Mouse IgG affinity gel is used as the control for CoIP experiment, and its properties are stable. The DYKDDDDK-Tag Rabbit pAb antibody has the advantages of high specificity, high affinity and high valence; Goat Anti-Rabbit IgG (peroxidase/HRP conjugated) is purified by cross-adsorption and only DYKDDDDK-Tag Rabbit pAb is identified, and there is no cross-reaction with the heavy-chain and light-chain of the mouse monoclonal antibody. The four components are strictly inspected and can be used independently; the combination of four sets has the advantages of fast, convenience and no interference band.
Immunoprecipitation (IP), Co-immunoprecipitation (Co-IP), Chromatin Immunoprecipitation (ChIP), and RNA-Binding Protein Immunoprecipitation (RIP) of Flag-tagged fusion proteins. The Flag tag can be located at the N-terminal and C-terminal, or the middle of the protein, such as the N-terminal Flag fusion protein (Flag–Protein) and the C-terminal Flag fusion protein (Protein-Flag).
GFP, a green fluorescent protein, is derived from Aequorea victoria multi tube luminous jellyfish and is composed of about 238 amino acids. It can stimulate green fluorescence from blue light to ultraviolet light. GFP is often used as a marker for recombinant expression of eukaryotic proteins. Anti-GFP Nanobody affinity gel is made by covalently coupling high-quality GFP nanobody with agarose gel. As the nanobody only contains the variable region of antibody molecules, there will be no signal interference from the heavy and light chains of the antibody during immuno (co) precipitation. It has the characteristics of high binding capacity of protein, high specificity and stability, and can be used for immuno (co) precipitation of GFP tagged fusion proteins.
GFP, a green fluorescent protein, is derived from Aequorea victoria multi tube luminous jellyfish and is composed of about 238 amino acids. It can stimulate green fluorescence from blue light to ultraviolet light. Anti-GFP nanobody immunomagnetic beads are made by covalently coupling high-quality GFP nanobody with magnetic beads，As the nano antibody only contains the variable region of antibody molecules, there will be no signal interference from the heavy and light chains of the antibody during immuno (co) precipitation. It has the characteristics of high binding capacity of protein, high specificity and stability, fast and convenient operation, and can be used for immuno (co) precipitation of GFP tagged fusion proteins.
Anti-GST Affinity Agarose, made of high-quality GST-tagged antibodies covalently conjugated to agarose gels, have the characteristics of high loading capacity, high specificity, stable properties, and can be used for affinity purification, immunoprecipitation (IP), co-immunoprecipitation (Co-IP) and other immunoprecipitation related experiments.
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