Protein Sample Preparation

Specifically designed for plant research and supplied with plant specific reagents, including reagents for removal of plant pigments and other natural products that may interfere with protein analysis. Extracts and solubilizes nearly all of the

Protein A is a cell-wall receptor which is present on cell wall of various starins of Staphyloccocus aureus. Protein A contains four high-affinity binding sites for interacting with the Fc region of immunoglobulin Gs of various species including

G-Biosciences&#39 Protein A Magnetic Beads are Fe₃O₄ beads coated with dextran to produce highly uniform, 1&microm beads. Recombinant Protein A is covalently coupled to the dextran coat to produce an enhanced alternative to

G-Biosciences&#39 Protein A Magnetic Beads are Fe₃O₄ beads coated with dextran to produce highly uniform, 1&microm beads. Recombinant Protein A is covalently coupled to the dextran coat to produce an enhanced alternative to

Immobilized Protein A is for binding the constant domains of immunoglobulin (Ig) molecules (seeFigure 1). Protein A is coupled to agarose beads by reductive amination method that provides high coupling efficiency for immunoglobulins and minimal

Immobilized Protein A is for binding the constant domains of immunoglobulin (Ig) molecules (seeFigure 1). Protein A is coupled to agarose beads by reductive amination method that provides high coupling efficiency for immunoglobulins and minimal

Immobilized Protein A is for binding the constant domains of immunoglobulin (Ig) molecules (seeFigure 1). Protein A is coupled to agarose beads by reductive amination method that provides high coupling efficiency for immunoglobulins and minimal

Immobilized Protein A is for binding the constant domains of immunoglobulin (Ig) molecules (seeFigure 1). Protein A is coupled to agarose beads by reductive amination method that provides high coupling efficiency for immunoglobulins and minimal

Immobilized Protein A is for binding the constant domains of immunoglobulin (Ig) molecules (seeFigure 1). Protein A is coupled to agarose beads by reductive amination method that provides high coupling efficiency for immunoglobulins and minimal

Immobilized Protein A is for binding the constant domains of immunoglobulin (Ig) molecules (seeFigure 1). Protein A is coupled to agarose beads by reductive amination method that provides high coupling efficiency for immunoglobulins and minimal

Immobilized Protein A is for binding the constant domains of immunoglobulin (Ig) molecules (seeFigure 1). Protein A is coupled to agarose beads by reductive amination method that provides high coupling efficiency for immunoglobulins and minimal

2D electrophoresis and mass spectrometry is routinely used for identification of novel proteins, however the greatest challenge in protein identification is achieving suitable resolution of proteins. The high dynamic range of a species&#39 proteome