
The method of isolation and some properties of the neutral protein activator of proliferation processes are described. The protein obtained is characterized by high lability and easily destroys treated with proteolytic enzymes and stored under any conditions. It loses the greater part of activity. Peptides formed differ in their properties from the proliferation peptide activators studied earlier and are not able to stimulate the proliferation processes in the brain tissue cells.
Molecular Weight, Chromatography, Gel, Animals, Brain, Nerve Tissue Proteins, Rats, Inbred Strains, Hydrogen-Ion Concentration, In Vitro Techniques, Isoelectric Focusing, Cell Division, Stimulation, Chemical, Rats
Molecular Weight, Chromatography, Gel, Animals, Brain, Nerve Tissue Proteins, Rats, Inbred Strains, Hydrogen-Ion Concentration, In Vitro Techniques, Isoelectric Focusing, Cell Division, Stimulation, Chemical, Rats
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