Secondary Antibodies

Goat polyclonal antibody raised against mouse IgG F(c) fragment. This secondary antibody generated in goat is a proteolytic fragment of immunoglobulin G (IgG) obtained by limited digestion with the enzyme papain under controlled conditions of temperature, time and pH. Receptors bind the Fc portion of mouse IgG and often this fragment is removed from immunoglobulins to minimize receptor binding and lower background reactivity. The antibody is conjugated with Horseradish Peroxidase (HRP).

Anti-Human IgG Fc (50D4), mAb, Mouse,1mg

Anti-Human IgG Fc (50D4), mAb, Mouse,10mg

Anti-Human IgG Fc (50D4), mAb, Mouse,100mg

Anti-Human IgM mu Chain (M3HC) ,1mg

Anti-Human IgM mu Chain (M3HC) ,10mg

Anti-Human IgM mu Chain (M3HC) ,100mg

TrueBlot® Magnetic Beads are uniform, non-aggregating, super-paramagnetic beads consisting of a ferric oxide core functionalized with various silane groups. The super-paramagnetic nanoparticles are coupled with a biomolecule, such as goat Anti-rabbit IgG, and are specifically designed, tested and quality controlled for isolation and purification of rabbit IgG, and immunoprecipitation methods using manual or automatic platforms. This antibody binds the heavy chain of all rabbit IgG subclasses and is suitable for immunoassays that utilize a rabbit IgG primary polyclonal antibody. Cell separation and sorting can be achieved using a rabbit IgG antibody to defined cell surface antigens. The beads have a large surface area with high capture efficiencies. The beads are in suspension and will settle upon storage. Prior to use, mix the vial gently (do not vortex) to ensure delivery of proper bead volume. Bead mean diameter is ~0.5 μm, bead concentration is 5 mg/mL.

TrueBlot® Magnetic Beads are uniform, non-aggregating, super-paramagnetic beads consisting of a ferric oxide core functionalized with various silane groups. The super-paramagnetic nanoparticles are coupled with a biomolecule, such as goat Anti-mouse IgG, and are specifically designed, tested and quality controlled for isolation and purification of mouse IgG, and immunoprecipitation methods using manual or automatic platforms. This antibody binds the heavy chain of mouse IgG and is suitable for immunoassays that utilize a mouse IgG primary polyclonal antibody. Cell separation and sorting can be achieved using a mouse IgG antibody to defined cell surface antigens. The beads have a large surface area with high capture efficiencies. The beads are in suspension and will settle upon storage. Prior to use, mix the vial gently (do not vortex) to ensure delivery of proper bead volume. Bead mean diameter is ~0.5 μm, bead concentration is 5 mg/mL.