This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

这种方法的运用是于首先使纯的生物分子结晶为有序排列然后用X射线分析结晶体。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

最常用的方法是通过端纳米结构的酰亚胺活合物来进行生物分子与1-D纳米结构的共价结合。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳香酯酶为研究对象可覆盖小分子、酶和蛋白大分子、核和因等对象和相应研究技术。

This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

这种方法的运用是于首先使纯的生物分子结晶为有序排列然后用X射线分析结晶体。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

最常用的方法是通过纳米结构的酰亚胺活氨物来进行生物分子与1-D纳米结构的共价结。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳香酯酶为研究对象可覆盖小分子、酶和蛋白大分子、核和因等对象和相应研究技术。

This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

这种方法的运用是基于首先使纯化的生物分子结有序排列然后用X射线分析结体。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

最常用的方法是通过端羧酸基纳米结构的酰亚胺活化氨基化合物来进行生物分子与1-D纳米结构的共价结合。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳研究对象可覆盖小分子、和蛋白大分子、核酸和基因等对象和相应研究技术。

This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

这种方法的运用是基于首先使纯化的生物分子结为有序排列然后用X射线分析结。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

常用的方法是通过端羧酸基结构的酰亚胺活化氨基化合物来进行生物分子1-D结构的共价结合。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳香酯酶为研究对象可覆盖小分子、酶和蛋白大分子、核酸和基因等对象和相应研究技术。

This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

这种方法的运于首先使纯化的生物分子结晶为有序排列然后X射线分析结晶体。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

最常的方法通过端羧酸纳米结构的酰亚胺活化氨化合物来进行生物分子与1-D纳米结构的共价结合。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳香酯酶为研究对象可覆盖小分子、酶大分子、核酸因等对象相应研究技术。

This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

这种法运是基于首先使纯化子结晶为有序排列然后X射线析结晶体。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

最常法是通过端羧酸基纳米结构酰亚胺活化氨基化合来进行子与1-D纳米结构共价结合。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳香酯酶为研究对象可覆盖小子、酶和蛋白大子、核酸和基因等对象和相应研究技术。

This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

方法的运用是于首先使纯化的生物分子结晶为有序排列然后用X射线分析结晶体。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

最常用的方法是通过端羧纳米结构的酰亚胺活化氨化合物来进行生物分子与1-D纳米结构的共价结合。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳香酯酶为研究对象可覆盖小分子、酶蛋白大分子、核因等对象相应研究技术。

This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

这种方法的运用是基于首先使纯化的生物分子有序排列然后用X射线分析体。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

最常用的方法是通过端羧酸基纳米构的酰亚胺活化氨基化合物来进行生物分子与1-D纳米构的共价合。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳香研究对象可覆盖小分子、和蛋白大分子、核酸和基因等对象和相应研究技术。

This is achieved by first crystallizing the purified biomolecule into ordered arrays and then using X-ray diffraction to analyze the crystals.

这种方法的运是基于首先使纯化的生物分子晶为有序排列然后X分析晶体。

The most commonly used method for the covalent binding of biomolecules onto 1-D nanostructures is through the diimide-activated amidation of carboxylic acid terminated nanostructures.

最常的方法是通过端羧酸基纳米构的酰亚胺活化氨基化合物来进行生物分子与1-D纳米构的合。

With serum arylesterase as the topics of teaching, small biomolecules, enzyme and protein, nucleic acids and genes as well as the techniques for their researches were covered.

以血清芳香酯酶为研究对象可覆盖小分子、酶和蛋白大分子、核酸和基因等对象和相应研究技术。