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。
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
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(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
。
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
素来消化双歧杆
壁,提取
粒,并与商业化
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.
结果球孢发酵液与溶
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,采用基因转染技术,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.
方法利用球孢发酵产生的变溶
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,
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壁,提取粒,并与商业化溶菌酶法比较。
声明:以上句、词
类均由互联网资源自动生成,部
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.
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。
:
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,采电穿孔基
技术,将重组EBV-LMP表达
粒
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
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
。
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
来消化双歧杆
壁,提取
粒,并与商业化
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。