Abstract
The experiment was made on the division of the sermoprotein by changing in many ways the density of the veronal buffer being used with the paperelectrochromatography. It was thereby found that the division of the figure of sermoprotein was in the best condition when the following buffers were employed:
1) Buffer A (pH 8.6) Veronal-Na 7.73g (Sodium-diethyl barbiturate) Veronal 1.38g (Diethyl barbituric acid) add Aq. dest. 1.000cc
2) Buffer B (pH8.5) Veronal-Na 11.76g (Sodium-diethyl barbiturate) Sodium Acetate 6.24g N/10 Acetic acid 107.7cc add Aq. dest, 2, 000cc
