pet-30a (+) expression vector (Millipore)
Millipore is a verified supplier 
90
Structured Review
Millipore
pet-30a (+) expression vector
Pet 30a (+) Expression Vector, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/the+pet+30a(+1+)+expression+vector/pet28a/10__1016_slash_j__pestbp__2024__106005-59-98-102
Average 90 stars, based on 1 article reviews
Pet 30a (+) Expression Vector, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/the+pet+30a(+1+)+expression+vector/pet28a/10__1016_slash_j__pestbp__2024__106005-59-98-102
Average 90 stars, based on 1 article reviews
pet-30a (+) expression vector - by Bioz Stars,
2026-10
90/100 stars
Images
Related Articles
Plasmid Preparation:Article Title: High-level expression and purification of immunogenic recombinant SAG1 (P30) of Toxoplasma gondii in Escherichia coli. Article Snippet: Surface antigen 1 (SAG1) of Toxoplasma gondii is a good candidate for diagnosis and vaccine development, but recombinant SAG1 produced in Escheichia coli often loses its specific immunogenicity due to the incorrect folding.. In the present study, a truncated SAG1 was highly expressed in E. coli as a fusion protein, about 30% of the total protein of the cell lysate.. After a simple purification and refolding procedure, purified rSAG1 can be recognized by human Tox- Article Title: Role of individual amino acids of apolipoprotein A-I in the activation of lecithin:cholesterol acyltransferase and in HDL rearrangements Article Snippet: Expression and purification of wild-type and mutant proteins The expression and purification of wild-type proapoA-I (WTproapoA-I) and mutant proapoA-I forms were carried out as described previously (18), using the pET 30a( 1 ) expression vector and Clone Assay:Article Title: High-level expression and purification of immunogenic recombinant SAG1 (P30) of Toxoplasma gondii in Escherichia coli. Article Snippet: Surface antigen 1 (SAG1) of Toxoplasma gondii is a good candidate for diagnosis and vaccine development, but recombinant SAG1 produced in Escheichia coli often loses its specific immunogenicity due to the incorrect folding.. In the present study, a truncated SAG1 was highly expressed in E. coli as a fusion protein, about 30% of the total protein of the cell lysate.. After a simple purification and refolding procedure, purified rSAG1 can be recognized by human Tox- Article Title: Role of individual amino acids of apolipoprotein A-I in the activation of lecithin:cholesterol acyltransferase and in HDL rearrangements Article Snippet: Expression and purification of wild-type and mutant proteins The expression and purification of wild-type proapoA-I (WTproapoA-I) and mutant proapoA-I forms were carried out as described previously (18), using the pET 30a( 1 ) expression vector and Expressing:Article Title: High-level expression and purification of immunogenic recombinant SAG1 (P30) of Toxoplasma gondii in Escherichia coli. Article Snippet: Surface antigen 1 (SAG1) of Toxoplasma gondii is a good candidate for diagnosis and vaccine development, but recombinant SAG1 produced in Escheichia coli often loses its specific immunogenicity due to the incorrect folding.. In the present study, a truncated SAG1 was highly expressed in E. coli as a fusion protein, about 30% of the total protein of the cell lysate.. After a simple purification and refolding procedure, purified rSAG1 can be recognized by human Tox- Article Title: Role of individual amino acids of apolipoprotein A-I in the activation of lecithin:cholesterol acyltransferase and in HDL rearrangements Article Snippet: Expression and purification of wild-type and mutant proteins The expression and purification of wild-type proapoA-I (WTproapoA-I) and mutant proapoA-I forms were carried out as described previously (18), using the pET 30a( 1 ) expression vector and Purification:Article Title: High-level expression and purification of immunogenic recombinant SAG1 (P30) of Toxoplasma gondii in Escherichia coli. Article Snippet: Surface antigen 1 (SAG1) of Toxoplasma gondii is a good candidate for diagnosis and vaccine development, but recombinant SAG1 produced in Escheichia coli often loses its specific immunogenicity due to the incorrect folding.. In the present study, a truncated SAG1 was highly expressed in E. coli as a fusion protein, about 30% of the total protein of the cell lysate.. After a simple purification and refolding procedure, purified rSAG1 can be recognized by human Tox- Article Title: Role of individual amino acids of apolipoprotein A-I in the activation of lecithin:cholesterol acyltransferase and in HDL rearrangements Article Snippet: Expression and purification of wild-type and mutant proteins The expression and purification of wild-type proapoA-I (WTproapoA-I) and mutant proapoA-I forms were carried out as described previously (18), using the pET 30a( 1 ) expression vector and Mutagenesis:Article Title: High-level expression and purification of immunogenic recombinant SAG1 (P30) of Toxoplasma gondii in Escherichia coli. Article Snippet: Surface antigen 1 (SAG1) of Toxoplasma gondii is a good candidate for diagnosis and vaccine development, but recombinant SAG1 produced in Escheichia coli often loses its specific immunogenicity due to the incorrect folding.. In the present study, a truncated SAG1 was highly expressed in E. coli as a fusion protein, about 30% of the total protein of the cell lysate.. After a simple purification and refolding procedure, purified rSAG1 can be recognized by human Tox- Article Title: Role of individual amino acids of apolipoprotein A-I in the activation of lecithin:cholesterol acyltransferase and in HDL rearrangements Article Snippet: Expression and purification of wild-type and mutant proteins The expression and purification of wild-type proapoA-I (WTproapoA-I) and mutant proapoA-I forms were carried out as described previously (18), using the pET 30a( 1 ) expression vector and |