cloning pcdna hisc mtaz addgene (Addgene inc)
Addgene inc is a verified supplier 
91
Structured Review
Addgene inc
cloning pcdna hisc mtaz addgene
Cloning Pcdna Hisc Mtaz Addgene, supplied by Addgene inc, used in various techniques. Bioz Stars score: 91/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/addgene+clones/pcDNA3%2E1%2FHisC-mTAZ+(Plasmid+%2331793)/pm41928626-296-163-165
Average 91 stars, based on 3 article reviews
Cloning Pcdna Hisc Mtaz Addgene, supplied by Addgene inc, used in various techniques. Bioz Stars score: 91/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/addgene+clones/pcDNA3%2E1%2FHisC-mTAZ+(Plasmid+%2331793)/pm41928626-296-163-165
Average 91 stars, based on 3 article reviews
cloning pcdna hisc mtaz addgene - by Bioz Stars,
2026-09
91/100 stars
Images
Related Articles
CRISPR:Article Title: Role for carbohydrate response element-binding protein (ChREBP) in high glucose-mediated repression of long noncoding RNA Tug1 Article Snippet: .. CRISPR/APEX-mediated proximity labeling and streptavidin pulldown—We engineered the dCas9-APEX2-NLS construct from two Labeling:Article Title: Role for carbohydrate response element-binding protein (ChREBP) in high glucose-mediated repression of long noncoding RNA Tug1 Article Snippet: .. CRISPR/APEX-mediated proximity labeling and streptavidin pulldown—We engineered the dCas9-APEX2-NLS construct from two Construct:Article Title: Role for carbohydrate response element-binding protein (ChREBP) in high glucose-mediated repression of long noncoding RNA Tug1 Article Snippet: .. CRISPR/APEX-mediated proximity labeling and streptavidin pulldown—We engineered the dCas9-APEX2-NLS construct from two Article Title: Enhanced transcriptional heterogeneity mediated by NF-κB super-enhancers. Article Snippet: The DT40 cells were cultured in RPMI-1640 without phenol red (Wako, Japan) supplemented with 10% fetal bovine serum (Sigma-Aldrich, USA), 1% (v/v) chicken serum (Nippon Bio-test Laboratories, Japan), 75 μM 2-mercaptoethanol (Gibco, USA), 1 mM sodium pyruvate (Wako, Japan), 1% (v/v) penicillin-streptomycin solution (Nacalai Tesque, Japan), 1% (v/v) 100x MEM non-essential amino acids solution (Wako), and 2 mM L-glutamine (Nacalai Tesque). .. The cells were cultured at 39 ̊C and 5% CO2 in a humidified incubator. mKate2-BRD4S transposon plasmid construction We engineered the PB-TA-ERP2-mKate2-BRD4S construct from two Clone Assay:Article Title: Role for carbohydrate response element-binding protein (ChREBP) in high glucose-mediated repression of long noncoding RNA Tug1 Article Snippet: .. CRISPR/APEX-mediated proximity labeling and streptavidin pulldown—We engineered the dCas9-APEX2-NLS construct from two Article Title: Enhanced transcriptional heterogeneity mediated by NF-κB super-enhancers. Article Snippet: The DT40 cells were cultured in RPMI-1640 without phenol red (Wako, Japan) supplemented with 10% fetal bovine serum (Sigma-Aldrich, USA), 1% (v/v) chicken serum (Nippon Bio-test Laboratories, Japan), 75 μM 2-mercaptoethanol (Gibco, USA), 1 mM sodium pyruvate (Wako, Japan), 1% (v/v) penicillin-streptomycin solution (Nacalai Tesque, Japan), 1% (v/v) 100x MEM non-essential amino acids solution (Wako), and 2 mM L-glutamine (Nacalai Tesque). .. The cells were cultured at 39 ̊C and 5% CO2 in a humidified incubator. mKate2-BRD4S transposon plasmid construction We engineered the PB-TA-ERP2-mKate2-BRD4S construct from two Article Title: Noncanonical roles of ATG5 and membrane atg8ylation in retromer assembly and function Article Snippet: Plasmids used in this study, such as ATG5 were generated by first cloning inserts into pDONR221 (Gateway Technology cloning vector, Thermo Scientfic) using a BP cloning reaction and the expression vectors were made utilizing LR cloning reaction (Gateway, Thermo Fisher) in appropriate (pDEST) destination vectors for immunoprecipitation assay. .. Article Title: Noncanonical roles of ATG5 and membrane atg8ylation in retromer assembly and function Article Snippet: Plasmids used in this study, such as ATG5 were generated by first cloning inserts into pDONR221 (Gateway Technology cloning vector, Thermo Scientfic) using a BP cloning reaction and the expression vectors were made utilizing LR cloning reaction (Gateway, Thermo Fisher) in appropriate (pDEST) destination vectors for immunoprecipitation assay. .. Expressing:Article Title: Role for carbohydrate response element-binding protein (ChREBP) in high glucose-mediated repression of long noncoding RNA Tug1 Article Snippet: .. CRISPR/APEX-mediated proximity labeling and streptavidin pulldown—We engineered the dCas9-APEX2-NLS construct from two Control:Article Title: Role for carbohydrate response element-binding protein (ChREBP) in high glucose-mediated repression of long noncoding RNA Tug1 Article Snippet: .. CRISPR/APEX-mediated proximity labeling and streptavidin pulldown—We engineered the dCas9-APEX2-NLS construct from two Sequencing:Article Title: Role for carbohydrate response element-binding protein (ChREBP) in high glucose-mediated repression of long noncoding RNA Tug1 Article Snippet: .. CRISPR/APEX-mediated proximity labeling and streptavidin pulldown—We engineered the dCas9-APEX2-NLS construct from two Cell Culture:Article Title: Enhanced transcriptional heterogeneity mediated by NF-κB super-enhancers. Article Snippet: The DT40 cells were cultured in RPMI-1640 without phenol red (Wako, Japan) supplemented with 10% fetal bovine serum (Sigma-Aldrich, USA), 1% (v/v) chicken serum (Nippon Bio-test Laboratories, Japan), 75 μM 2-mercaptoethanol (Gibco, USA), 1 mM sodium pyruvate (Wako, Japan), 1% (v/v) penicillin-streptomycin solution (Nacalai Tesque, Japan), 1% (v/v) 100x MEM non-essential amino acids solution (Wako), and 2 mM L-glutamine (Nacalai Tesque). .. The cells were cultured at 39 ̊C and 5% CO2 in a humidified incubator. mKate2-BRD4S transposon plasmid construction We engineered the PB-TA-ERP2-mKate2-BRD4S construct from two Plasmid Preparation:Article Title: Enhanced transcriptional heterogeneity mediated by NF-κB super-enhancers. Article Snippet: The DT40 cells were cultured in RPMI-1640 without phenol red (Wako, Japan) supplemented with 10% fetal bovine serum (Sigma-Aldrich, USA), 1% (v/v) chicken serum (Nippon Bio-test Laboratories, Japan), 75 μM 2-mercaptoethanol (Gibco, USA), 1 mM sodium pyruvate (Wako, Japan), 1% (v/v) penicillin-streptomycin solution (Nacalai Tesque, Japan), 1% (v/v) 100x MEM non-essential amino acids solution (Wako), and 2 mM L-glutamine (Nacalai Tesque). .. The cells were cultured at 39 ̊C and 5% CO2 in a humidified incubator. mKate2-BRD4S transposon plasmid construction We engineered the PB-TA-ERP2-mKate2-BRD4S construct from two |