pbabe krasg12d plasmid (Addgene inc)
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Addgene inc
pbabe krasg12d plasmid
Pbabe Krasg12d Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 41 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pbabe+krasg12d+plasmid/pBabe-Kras+G12D+(Plasmid+%2358902)/bio_rxiv__64898__2026__03__24__711280-204-3-11
Average 93 stars, based on 41 article reviews
Pbabe Krasg12d Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 41 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pbabe+krasg12d+plasmid/pBabe-Kras+G12D+(Plasmid+%2358902)/bio_rxiv__64898__2026__03__24__711280-204-3-11
Average 93 stars, based on 41 article reviews
pbabe krasg12d plasmid - by Bioz Stars,
2026-09
93/100 stars
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Related Articles
Plasmid Preparation:Article Title: Cell-of-Origin, not Oncogenic Effect, Determines Desmoplastic Immune Exclusion in KRAS-Driven Liver Cancer Article Snippet: .. [ ] The Article Title: A systematic genome-wide mapping of oncogenic mutation selection during CRISPR-Cas9 genome editing Article Snippet: .. Constructs and stable cell lines MOLM13 cells were obtained from DSMZ (Cat. ACC-554) and maintained in RPMI-1640 medium (Life Technologies, Carlsbad, CA) supplemented with 10% v/v heat-inactivated fetal bovine serum (Sigma-Aldrich, Saint Louis, MI), 2 mM L-Glutamine (LifeTechnologies) and 100 U/mL penicillin/streptomycin (LifeTechnologies). p53 R248Q was PCR ampli ed from a bacterial expression plasmid (kind gift of Dr. Shannon Lauberth, UCSD) and KRASG12D the Article Title: Therapeutically reprogrammed nutrient signalling enhances nanoparticulate albumin bound drug uptake and efficacy in KRAS-mutant cancer. Article Snippet: KP or iKras cells stably expressing ERK-KTR, referred to as KP ERK-KTR or iKras ERK-KTR, respectively, were selected with growth media containing 10 μg ml−1 puromycin (Invitrogen) for 7 d and subsequently sorted for cells with high expression of fluorescent proteins via fluorescence activated cell sorting (FACS, MGH Flow Cytometry Core). .. BxPC-3 cells transiently expressing KrasG12D mutation were generated by transfecting parental BxPC-3 cells with Construct:Article Title: A systematic genome-wide mapping of oncogenic mutation selection during CRISPR-Cas9 genome editing Article Snippet: .. Constructs and stable cell lines MOLM13 cells were obtained from DSMZ (Cat. ACC-554) and maintained in RPMI-1640 medium (Life Technologies, Carlsbad, CA) supplemented with 10% v/v heat-inactivated fetal bovine serum (Sigma-Aldrich, Saint Louis, MI), 2 mM L-Glutamine (LifeTechnologies) and 100 U/mL penicillin/streptomycin (LifeTechnologies). p53 R248Q was PCR ampli ed from a bacterial expression plasmid (kind gift of Dr. Shannon Lauberth, UCSD) and KRASG12D the Stable Transfection:Article Title: A systematic genome-wide mapping of oncogenic mutation selection during CRISPR-Cas9 genome editing Article Snippet: .. Constructs and stable cell lines MOLM13 cells were obtained from DSMZ (Cat. ACC-554) and maintained in RPMI-1640 medium (Life Technologies, Carlsbad, CA) supplemented with 10% v/v heat-inactivated fetal bovine serum (Sigma-Aldrich, Saint Louis, MI), 2 mM L-Glutamine (LifeTechnologies) and 100 U/mL penicillin/streptomycin (LifeTechnologies). p53 R248Q was PCR ampli ed from a bacterial expression plasmid (kind gift of Dr. Shannon Lauberth, UCSD) and KRASG12D the Polymerase Chain Reaction:Article Title: A systematic genome-wide mapping of oncogenic mutation selection during CRISPR-Cas9 genome editing Article Snippet: .. Constructs and stable cell lines MOLM13 cells were obtained from DSMZ (Cat. ACC-554) and maintained in RPMI-1640 medium (Life Technologies, Carlsbad, CA) supplemented with 10% v/v heat-inactivated fetal bovine serum (Sigma-Aldrich, Saint Louis, MI), 2 mM L-Glutamine (LifeTechnologies) and 100 U/mL penicillin/streptomycin (LifeTechnologies). p53 R248Q was PCR ampli ed from a bacterial expression plasmid (kind gift of Dr. Shannon Lauberth, UCSD) and KRASG12D the Expressing:Article Title: A systematic genome-wide mapping of oncogenic mutation selection during CRISPR-Cas9 genome editing Article Snippet: .. Constructs and stable cell lines MOLM13 cells were obtained from DSMZ (Cat. ACC-554) and maintained in RPMI-1640 medium (Life Technologies, Carlsbad, CA) supplemented with 10% v/v heat-inactivated fetal bovine serum (Sigma-Aldrich, Saint Louis, MI), 2 mM L-Glutamine (LifeTechnologies) and 100 U/mL penicillin/streptomycin (LifeTechnologies). p53 R248Q was PCR ampli ed from a bacterial expression plasmid (kind gift of Dr. Shannon Lauberth, UCSD) and KRASG12D the Article Title: Therapeutically reprogrammed nutrient signalling enhances nanoparticulate albumin bound drug uptake and efficacy in KRAS-mutant cancer. Article Snippet: KP or iKras cells stably expressing ERK-KTR, referred to as KP ERK-KTR or iKras ERK-KTR, respectively, were selected with growth media containing 10 μg ml−1 puromycin (Invitrogen) for 7 d and subsequently sorted for cells with high expression of fluorescent proteins via fluorescence activated cell sorting (FACS, MGH Flow Cytometry Core). .. BxPC-3 cells transiently expressing KrasG12D mutation were generated by transfecting parental BxPC-3 cells with Mutagenesis:Article Title: Therapeutically reprogrammed nutrient signalling enhances nanoparticulate albumin bound drug uptake and efficacy in KRAS-mutant cancer. Article Snippet: KP or iKras cells stably expressing ERK-KTR, referred to as KP ERK-KTR or iKras ERK-KTR, respectively, were selected with growth media containing 10 μg ml−1 puromycin (Invitrogen) for 7 d and subsequently sorted for cells with high expression of fluorescent proteins via fluorescence activated cell sorting (FACS, MGH Flow Cytometry Core). .. BxPC-3 cells transiently expressing KrasG12D mutation were generated by transfecting parental BxPC-3 cells with Generated:Article Title: Therapeutically reprogrammed nutrient signalling enhances nanoparticulate albumin bound drug uptake and efficacy in KRAS-mutant cancer. Article Snippet: KP or iKras cells stably expressing ERK-KTR, referred to as KP ERK-KTR or iKras ERK-KTR, respectively, were selected with growth media containing 10 μg ml−1 puromycin (Invitrogen) for 7 d and subsequently sorted for cells with high expression of fluorescent proteins via fluorescence activated cell sorting (FACS, MGH Flow Cytometry Core). .. BxPC-3 cells transiently expressing KrasG12D mutation were generated by transfecting parental BxPC-3 cells with |