Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉菌发酵液与溶菌酶均成功提取到粒。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉菌发酵液与溶菌酶均成功提取到粒。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
以人高分化鼻咽癌细胞株(CNE1)为对象,采用电穿孔基因转,将重组EBV-LMP表达
粒转
CNE1细胞。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
法
用球孢链霉菌发酵产生的变溶菌素来消化双歧杆菌细胞壁,提取
粒,并与商业化溶菌酶法比较。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉发酵液与溶
酶均成功提取到
。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
人高分化鼻咽癌
株(CNE1)为对象,采用电穿孔基因转染技术,将重组EBV-LMP表达
转染CNE1
。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
方法利用球孢链霉发酵产生的变溶
素来消化双歧杆
壁,提取
,并与商业化溶
酶法比较。
声明:上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉液与溶
均成功提取到
粒。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
以人高分化鼻咽癌细胞株(CNE1)为对象,采用电穿孔基因转染技术,将重组EBV-LMP表达粒转染CNE1细胞。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
方法利用球孢链霉产生的变溶
素来消化双歧杆
细胞壁,提取
粒,并与商业化溶
法比较。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若现问题,欢迎向我们指正。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉菌发酵液与溶菌酶均成功提取。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
以人高分化鼻咽癌株(CNE1)为对象,采用电穿孔基因转染技术,将重组EBV-LMP表达
转染CNE1
。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
方法利用球孢链霉菌发酵产生的变溶菌素来消化双歧杆菌,提取
,并与商业化溶菌酶法比较。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉与
均成功提取到
粒。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
以人高分化鼻咽癌细胞株(CNE1)为对象,采用电穿孔基因转染技术,将重组EBV-LMP表达粒转染CNE1细胞。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
方法利用球孢链霉产生的变
素来消化双歧杆
细胞壁,提取
粒,并与商业化
法比较。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若现问题,欢迎向我们指正。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉液与溶
酶均成功提取到
粒。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
以人高分化鼻咽癌细胞株(CNE1)为对象,穿孔基因转染技术,将重组EBV-LMP表达
粒转染CNE1细胞。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
方法利球孢链霉
产生的变溶
素来消化双歧杆
细胞壁,提取
粒,并与商业化溶
酶法比较。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若现问题,欢迎向我们指正。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉与
均成功提取到
粒。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
以人高分化鼻咽癌细胞株(CNE1)为对象,采用电穿孔基因转染技术,将重组EBV-LMP表达粒转染CNE1细胞。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
方法利用球孢链霉产生的变
素来消化双歧杆
细胞壁,提取
粒,并与商业化
法比较。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若现问题,欢迎向我们指正。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉发酵液与溶
酶均成功提取到
。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
高分化鼻咽癌
胞株(CNE1)为对象,采用电穿孔基因转染技术,将重组EBV-LMP表达
转染CNE1
胞。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
方法利用球孢链霉发酵产生的变溶
素来消化双歧
胞壁,提取
,并与商业化溶
酶法比较。
声明:上例句、词性分类均由互联网资源自动生成,部分未经过
工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
Result Both mutanolysin and lysozyme could successfully lyse the wall of bifidobacterium and extract the plasmid from Bifidobacterium.
结果球孢链霉菌发酵液与溶菌酶均成功粒。
NPC cell line (CNE1) as target,Electroporation was used to transfect EBV-LMP gene and the vector into CNE1 cells.
以人高分化鼻咽癌细胞株(CNE1)为对象,采用电穿孔基因转染技术,将重组EBV-LMP表达粒转染CNE1细胞。
Method Bifidobacterium plasmid was extracted by mutanolysin from Streptomyces globisporus which could lyse the wall of bifidobacterium.The result was compared with that by lysozyme.
方法利用球孢链霉菌发酵产生的变溶菌素来消化双歧杆菌细胞,
粒,并与商业化溶菌酶法比较。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。