This product was prepared from normal serum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by papain digestion and extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Horse Serum, anti-Horse IgG and anti-Horse IgG F(ab')2. No reaction was observed against anti-Horse IgG F(c) or anti-Papain.
Size
2 mg
Concentration
2.0 mg/mL
Applications
Horse IgG Fab Fragment can be utilized as a control or standard reagent in Western Blotting and ELISA experiments.