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双歧杆菌细胞壁,提取
粒,并与商业
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.
结果球孢链霉菌发酵菌酶均成功提取到
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菌素来消
双歧杆菌细胞壁,提取
粒,并
商业
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
染技术,将重组EBV-LMP表达
粒
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),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
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溶菌
功提取到
。
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,
商业化溶菌
法比较。
声明:以上例句、词性分类由互联网资源自动生
,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(CNE1)
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
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杆菌细胞壁,提取
粒,并与商业
溶菌酶法比较。
声明:以上例句、词性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。