Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过自组装修饰金极界面微分充容覆盖率考察了NS在环己烷中自组装成动力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清蛋交联法将青霉素酶、纳米金胶氧化苏木精同时修饰在铂极上,制成化学生物传感器。

Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过自组装修饰金电极的界面微分充电电容和膜的覆盖率考察了NS在环己烷中自组装膜的成膜动力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清蛋交法将青霉素酶、纳米金胶和氧化苏木精同时修饰在铂电极上,制成电流型电化学生物传感器。

Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过自组装修饰金电极的界面微充电电容和膜的覆盖率考察了NS在环己烷中自组装膜的成膜动力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清蛋交联法将青霉素酶、纳米金胶和氧化苏木精同时修饰在铂电极上,制成电流型电化学生物传感器。

Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过自组装修饰金电极的界面微分充电电容的覆盖率考察了NS在环己烷中自组装的力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清蛋交联法将青霉素酶、纳米金化苏木精同时修饰在铂电极上,制电流型电化学生物传感器。

Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过自组装修极的界面微分充容和膜的覆盖率考察了NS在环己烷中自组装膜的成膜动力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清蛋交联法将青霉素酶、纳米胶和氧化苏木精同时修在铂极,制成流型化学生物传感器。

Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过自组装修饰金电极的界面微分充电电容和膜的覆盖率考察了NS在环己烷中自组装膜的成膜动力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清蛋交联法将青霉素酶、纳米金胶和氧化苏木精同时修饰在铂电极上,制成电流型电化学生物传感器。

Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过组装修饰金电极的界面微分充电电容和膜的覆盖率考察了NS在环己烷中组装膜的成膜力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清蛋交联法将青霉素酶、纳米金胶和氧化苏木精同时修饰在铂电极上,制成电流型电化学物传感器。

Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过自组装修饰金电极的界面微分充电电容和膜的覆盖率考察了NS在环己烷中自组装膜的成膜动力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清蛋交法将青霉素酶、纳米金胶和氧化苏木精同时修饰在铂电极上,制成电流型电化学生物传感器。

Using electrode interface capacitance and surface coverage to investigate the formation kinetics of NS monolayer in hexahydrobenzene solvent.

通过自组装修饰金电极的界面微分充电电容和膜的覆盖率考察了NS在环己烷中自组装膜的成膜动力学。

Penicillinase,hematein and nano gold colloid were immobilized,as a modified membrane,on a plane Pt electrode by glutaraldehyde-bovine serum albumin.

用戊二醛-牛血清法将青霉素酶、纳米金胶和氧化苏木精同时修饰在铂电极上,制成电流型电化学生物传感器。