px458 plasmid Search Results


96
Addgene inc crispr cas9 genomic engineering idt star methods rbns primers idt star methods recombinant dna px458 addgene plasmid
Crispr Cas9 Genomic Engineering Idt Star Methods Rbns Primers Idt Star Methods Recombinant Dna Px458 Addgene Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/px458+plasmid/pSpCas9(BB)-2A-GFP+(PX458)+(Plasmid+%2348138)/pm41932309-792-83-97
Average 96 stars, based on 1 article reviews
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Addgene inc px458 sgrna
Px458 Sgrna, supplied by Addgene inc, 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/px458+plasmid/pX458-sgRNA_Ago1_1+(Plasmid+%2373533)/pmc09442311-186-6-9
Average 90 stars, based on 1 article reviews
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Addgene inc inactivated control plasmid pspdcas9 hudtet1cd t2a mcherry
Inactivated Control Plasmid Pspdcas9 Hudtet1cd T2a Mcherry, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Addgene inc cells with px458 2a gfp sgrna trim25 g1
Cells With Px458 2a Gfp Sgrna Trim25 G1, supplied by Addgene inc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Addgene inc hek293t cells
Hek293t Cells, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/px458+plasmid/px458_2A_GFP_sgRNA_ELAVL1+(Plasmid+%23106106)/bio_rxiv__2025__03__01__640932-247-0-22
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Addgene inc px458 plasmid
Px458 Plasmid, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/px458+plasmid/PX458-AAVS1+(Plasmid+%23113194)/pm37950242-80-20-25
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Addgene inc fncas9 addgene 130969
schematic of the process that was optimized for <t>FnCas9-based</t> HDR-mediated endogenous tagging of the selected marker gene, DCX. The linearized donor DNA template used for knock-in is shown with various components, along with left and right homology arms complementary to the C-terminus end of the DCX . The agarose gel shows PCR genotyping of the antibiotic-selected cells with the successful integration of the DNA donor template. (NTC, no DNA template control)
Fncas9 Addgene 130969, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/px458+plasmid/PX458-3xHA-FnCas9+(Plasmid+%23130969)/bio_rxiv__2025__01__09__631995-134-3-4
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Addgene inc px458 ruby
schematic of the process that was optimized for <t>FnCas9-based</t> HDR-mediated endogenous tagging of the selected marker gene, DCX. The linearized donor DNA template used for knock-in is shown with various components, along with left and right homology arms complementary to the C-terminus end of the DCX . The agarose gel shows PCR genotyping of the antibiotic-selected cells with the successful integration of the DNA donor template. (NTC, no DNA template control)
Px458 Ruby, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Addgene inc px458 ef1a cas9 h2b gfp vector
schematic of the process that was optimized for <t>FnCas9-based</t> HDR-mediated endogenous tagging of the selected marker gene, DCX. The linearized donor DNA template used for knock-in is shown with various components, along with left and right homology arms complementary to the C-terminus end of the DCX . The agarose gel shows PCR genotyping of the antibiotic-selected cells with the successful integration of the DNA donor template. (NTC, no DNA template control)
Px458 Ef1a Cas9 H2b Gfp Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/px458+plasmid/pX458-Ef1a-Cas9-H2B-GFP+(Plasmid+%23159654)/10__1523_slash_eneuro__0391___23__2024-102-22-24
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92
Addgene inc solle
schematic of the process that was optimized for <t>FnCas9-based</t> HDR-mediated endogenous tagging of the selected marker gene, DCX. The linearized donor DNA template used for knock-in is shown with various components, along with left and right homology arms complementary to the C-terminus end of the DCX . The agarose gel shows PCR genotyping of the antibiotic-selected cells with the successful integration of the DNA donor template. (NTC, no DNA template control)
Solle, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/px458+plasmid/PX458_KMT2B_1+(Plasmid+%23101074)/pm39571574-745-26-53
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Addgene inc px458 sgrna ago1 3
Immunoblot analysis of DROSHA, DICER, <t>AGO1,</t> and AGO2 in WT and their respective KO mESC lines. TUBULIN was used as a loading control. Representative blot of three independent experiments is shown. PCA of gene expression as measured by RNA sequencing in miRNA _KO and WT samples. Biological replicates are indicated with corresponding colors. MA plots of the DGE analysis in miRNA _KO mutants versus WT. Significant up‐ and downregulated genes are colored in red and blue, respectively. Overlap of up‐ (left) and downregulated (right) genes in miRNA _KO mESCs. Comparison of miRNA loading for small RNA sequencing (Input) versus Argonaute2 & 1 (AGOs) RNA immunoprecipitation (RIP) and sequencing for all miRNAs. MiRNAs that show statistically significant difference between the two measured (adjusted P ‐value < 0.1) are highlighted. Data information: In (C and E), significance in differential analysis was determined using an adjusted P ‐value threshold obtained from DESeq2 of 0.1. In (D), an adjusted P ‐value threshold of 0.2 was applied. Source data are available online for this figure.
Px458 Sgrna Ago1 3, supplied by Addgene inc, 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/px458+plasmid/pX458-sgRNA_Ago1_3+(Plasmid+%2373535)/pmc09442311-10-0-4
Average 90 stars, based on 1 article reviews
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Image Search Results


schematic of the process that was optimized for FnCas9-based HDR-mediated endogenous tagging of the selected marker gene, DCX. The linearized donor DNA template used for knock-in is shown with various components, along with left and right homology arms complementary to the C-terminus end of the DCX . The agarose gel shows PCR genotyping of the antibiotic-selected cells with the successful integration of the DNA donor template. (NTC, no DNA template control)

Journal: bioRxiv

Article Title: Endogenous gene tagging with FnCas9 to track and sort neural lineages from 3D cortical organoids

doi: 10.1101/2025.01.09.631995

Figure Lengend Snippet: schematic of the process that was optimized for FnCas9-based HDR-mediated endogenous tagging of the selected marker gene, DCX. The linearized donor DNA template used for knock-in is shown with various components, along with left and right homology arms complementary to the C-terminus end of the DCX . The agarose gel shows PCR genotyping of the antibiotic-selected cells with the successful integration of the DNA donor template. (NTC, no DNA template control)

Article Snippet: The plasmid containing FnCas9 Addgene 130969 ( ) was incorporated with a crRNA sequence targeting the DCX C-terminus at the gRNA scaffold and was confirmed with PCR genotyping as well as Sanger sequencing.

Techniques: Marker, Knock-In, Agarose Gel Electrophoresis, Control

a) Schematic of the protocol optimized for the development of cortical organoids from the FnCas9-tagged hESCs (details in the “Methods” section). b) Left panel: expression of Ki67 and SOX2, highlighting the neural rosette cells and different developmental stages of cortical organoids (hCOs) at days 25, 52, and 75. Right panel: co-immunostaining of the organoid sections with neural marker proteins at days 25 and 60 showing their maturation (scale: 50 µm) c) Immunofluorescence-based co-localization of DCX and tdTomato expression within the cells dissociated from DCX-tdTomato-hCOs. (scale: 25 µm) d) The colocalization between the signals obtained from Red: Green channels are quantified as tM (thresholded Mander’s split colocalization coefficient), n = 30, error bars represent S.E.M., a single-mean two-tailed unpaired t-test is applied, and p values of **** ≤ 0.0001 (values from independent measurements are represented as dots). e) Real-time FACS-based cell sorting of live cells from DCX-tdTomato-tagged hCOs and unedited hCOs at day 52 (representative of three independent experiments).

Journal: bioRxiv

Article Title: Endogenous gene tagging with FnCas9 to track and sort neural lineages from 3D cortical organoids

doi: 10.1101/2025.01.09.631995

Figure Lengend Snippet: a) Schematic of the protocol optimized for the development of cortical organoids from the FnCas9-tagged hESCs (details in the “Methods” section). b) Left panel: expression of Ki67 and SOX2, highlighting the neural rosette cells and different developmental stages of cortical organoids (hCOs) at days 25, 52, and 75. Right panel: co-immunostaining of the organoid sections with neural marker proteins at days 25 and 60 showing their maturation (scale: 50 µm) c) Immunofluorescence-based co-localization of DCX and tdTomato expression within the cells dissociated from DCX-tdTomato-hCOs. (scale: 25 µm) d) The colocalization between the signals obtained from Red: Green channels are quantified as tM (thresholded Mander’s split colocalization coefficient), n = 30, error bars represent S.E.M., a single-mean two-tailed unpaired t-test is applied, and p values of **** ≤ 0.0001 (values from independent measurements are represented as dots). e) Real-time FACS-based cell sorting of live cells from DCX-tdTomato-tagged hCOs and unedited hCOs at day 52 (representative of three independent experiments).

Article Snippet: The plasmid containing FnCas9 Addgene 130969 ( ) was incorporated with a crRNA sequence targeting the DCX C-terminus at the gRNA scaffold and was confirmed with PCR genotyping as well as Sanger sequencing.

Techniques: Expressing, Immunostaining, Marker, Immunofluorescence, Two Tailed Test, FACS

Immunoblot analysis of DROSHA, DICER, AGO1, and AGO2 in WT and their respective KO mESC lines. TUBULIN was used as a loading control. Representative blot of three independent experiments is shown. PCA of gene expression as measured by RNA sequencing in miRNA _KO and WT samples. Biological replicates are indicated with corresponding colors. MA plots of the DGE analysis in miRNA _KO mutants versus WT. Significant up‐ and downregulated genes are colored in red and blue, respectively. Overlap of up‐ (left) and downregulated (right) genes in miRNA _KO mESCs. Comparison of miRNA loading for small RNA sequencing (Input) versus Argonaute2 & 1 (AGOs) RNA immunoprecipitation (RIP) and sequencing for all miRNAs. MiRNAs that show statistically significant difference between the two measured (adjusted P ‐value < 0.1) are highlighted. Data information: In (C and E), significance in differential analysis was determined using an adjusted P ‐value threshold obtained from DESeq2 of 0.1. In (D), an adjusted P ‐value threshold of 0.2 was applied. Source data are available online for this figure.

Journal: EMBO Reports

Article Title: Global and precise identification of functional miRNA targets in mESCs by integrative analysis

doi: 10.15252/embr.202254762

Figure Lengend Snippet: Immunoblot analysis of DROSHA, DICER, AGO1, and AGO2 in WT and their respective KO mESC lines. TUBULIN was used as a loading control. Representative blot of three independent experiments is shown. PCA of gene expression as measured by RNA sequencing in miRNA _KO and WT samples. Biological replicates are indicated with corresponding colors. MA plots of the DGE analysis in miRNA _KO mutants versus WT. Significant up‐ and downregulated genes are colored in red and blue, respectively. Overlap of up‐ (left) and downregulated (right) genes in miRNA _KO mESCs. Comparison of miRNA loading for small RNA sequencing (Input) versus Argonaute2 & 1 (AGOs) RNA immunoprecipitation (RIP) and sequencing for all miRNAs. MiRNAs that show statistically significant difference between the two measured (adjusted P ‐value < 0.1) are highlighted. Data information: In (C and E), significance in differential analysis was determined using an adjusted P ‐value threshold obtained from DESeq2 of 0.1. In (D), an adjusted P ‐value threshold of 0.2 was applied. Source data are available online for this figure.

Article Snippet: pX458‐sgRNA_ Ago1 _3 , Addgene , #73535.

Techniques: Western Blot, Control, Gene Expression, RNA Sequencing, Comparison, RNA Immunoprecipitation, Sequencing

Journal: EMBO Reports

Article Title: Global and precise identification of functional miRNA targets in mESCs by integrative analysis

doi: 10.15252/embr.202254762

Figure Lengend Snippet:

Article Snippet: pX458‐sgRNA_ Ago1 _3 , Addgene , #73535.

Techniques: Recombinant