Review



cas9 plasmid dna  (Thermo Fisher)


Bioz Verified Symbol Thermo Fisher is a verified supplier
Bioz Manufacturer Symbol Thermo Fisher manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 99

    Structured Review

    Thermo Fisher cas9 plasmid dna
    Construction and characterization of <t>CRISPR/Cas9-mediated</t> genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.
    Cas9 Plasmid Dna, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 468036 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cas9 plasmid dna/product/Thermo Fisher
    Average 99 stars, based on 468036 article reviews
    cas9 plasmid dna - by Bioz Stars, 2026-03
    99/100 stars

    Images

    1) Product Images from "CRISPR/Cas9-mediated deletion of MADD induces cell cycle arrest and apoptosis in anaplastic thyroid cancer cells"

    Article Title: CRISPR/Cas9-mediated deletion of MADD induces cell cycle arrest and apoptosis in anaplastic thyroid cancer cells

    Journal: Scientific Reports

    doi: 10.1038/s41598-025-22907-1

    Construction and characterization of CRISPR/Cas9-mediated genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.
    Figure Legend Snippet: Construction and characterization of CRISPR/Cas9-mediated genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.

    Techniques Used: CRISPR, Knock-Out, Control, Western Blot, Expressing, Immunocytochemistry, Cell Culture, Sterility, Staining



    Similar Products

    99
    Thermo Fisher cas9 plasmid dna
    Construction and characterization of <t>CRISPR/Cas9-mediated</t> genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.
    Cas9 Plasmid Dna, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cas9 plasmid dna/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    cas9 plasmid dna - by Bioz Stars, 2026-03
    99/100 stars
      Buy from Supplier

    90
    Addgene inc cas9 dna fragment in plasmid 46168
    Construction and characterization of <t>CRISPR/Cas9-mediated</t> genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.
    Cas9 Dna Fragment In Plasmid 46168, 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/result/cas9 dna fragment in plasmid 46168/product/Addgene inc
    Average 90 stars, based on 1 article reviews
    cas9 dna fragment in plasmid 46168 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    93
    Addgene inc paper n a recombinant dna px458 ef1a cas9 h2b mcherry addgene
    Construction and characterization of <t>CRISPR/Cas9-mediated</t> genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.
    Paper N A Recombinant Dna Px458 Ef1a Cas9 H2b Mcherry Addgene, 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/result/paper n a recombinant dna px458 ef1a cas9 h2b mcherry addgene/product/Addgene inc
    Average 93 stars, based on 1 article reviews
    paper n a recombinant dna px458 ef1a cas9 h2b mcherry addgene - by Bioz Stars, 2026-03
    93/100 stars
      Buy from Supplier

    95
    Addgene inc recombinant dna cyclin k egfp addgene 169930 pcw cas9 addgene 50661 plx sgrna addgene 50662 extended knockout eko
    Construction and characterization of <t>CRISPR/Cas9-mediated</t> genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.
    Recombinant Dna Cyclin K Egfp Addgene 169930 Pcw Cas9 Addgene 50661 Plx Sgrna Addgene 50662 Extended Knockout Eko, supplied by Addgene inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/recombinant dna cyclin k egfp addgene 169930 pcw cas9 addgene 50661 plx sgrna addgene 50662 extended knockout eko/product/Addgene inc
    Average 95 stars, based on 1 article reviews
    recombinant dna cyclin k egfp addgene 169930 pcw cas9 addgene 50661 plx sgrna addgene 50662 extended knockout eko - by Bioz Stars, 2026-03
    95/100 stars
      Buy from Supplier

    93
    Addgene inc n a n a recombinant dna lsl cas9 rosa26tv addgene
    Construction and characterization of <t>CRISPR/Cas9-mediated</t> genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.
    N A N A Recombinant Dna Lsl Cas9 Rosa26tv Addgene, 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/result/n a n a recombinant dna lsl cas9 rosa26tv addgene/product/Addgene inc
    Average 93 stars, based on 1 article reviews
    n a n a recombinant dna lsl cas9 rosa26tv addgene - by Bioz Stars, 2026-03
    93/100 stars
      Buy from Supplier

    90
    Santa Cruz Biotechnology crispr-cas9 plasmid dna targeting murine rig-i
    Construction and characterization of <t>CRISPR/Cas9-mediated</t> genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.
    Crispr Cas9 Plasmid Dna Targeting Murine Rig I, supplied by Santa Cruz Biotechnology, 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/result/crispr-cas9 plasmid dna targeting murine rig-i/product/Santa Cruz Biotechnology
    Average 90 stars, based on 1 article reviews
    crispr-cas9 plasmid dna targeting murine rig-i - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    93
    Addgene inc recombinant dna

    Recombinant Dna, 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/result/recombinant dna/product/Addgene inc
    Average 93 stars, based on 1 article reviews
    recombinant dna - by Bioz Stars, 2026-03
    93/100 stars
      Buy from Supplier

    96
    Addgene inc n a n a recombinant dna 3xha turboid nls pcdna3 addgene 107171 3xha miniturbo nls pcdna3 addgene 107172 pcrispaint taggfp2 puror addgene 80970

    N A N A Recombinant Dna 3xha Turboid Nls Pcdna3 Addgene 107171 3xha Miniturbo Nls Pcdna3 Addgene 107172 Pcrispaint Taggfp2 Puror Addgene 80970, 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/result/n a n a recombinant dna 3xha turboid nls pcdna3 addgene 107171 3xha miniturbo nls pcdna3 addgene 107172 pcrispaint taggfp2 puror addgene 80970/product/Addgene inc
    Average 96 stars, based on 1 article reviews
    n a n a recombinant dna 3xha turboid nls pcdna3 addgene 107171 3xha miniturbo nls pcdna3 addgene 107172 pcrispaint taggfp2 puror addgene 80970 - by Bioz Stars, 2026-03
    96/100 stars
      Buy from Supplier

    99
    Thermo Fisher cas9 2a gfp plasmid dna

    Cas9 2a Gfp Plasmid Dna, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cas9 2a gfp plasmid dna/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    cas9 2a gfp plasmid dna - by Bioz Stars, 2026-03
    99/100 stars
      Buy from Supplier

    Image Search Results


    Construction and characterization of CRISPR/Cas9-mediated genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.

    Journal: Scientific Reports

    Article Title: CRISPR/Cas9-mediated deletion of MADD induces cell cycle arrest and apoptosis in anaplastic thyroid cancer cells

    doi: 10.1038/s41598-025-22907-1

    Figure Lengend Snippet: Construction and characterization of CRISPR/Cas9-mediated genomic knockout of MADD gene in ATC Cells: ( A ) Schematic diagram of the construction of CRISPR/Cas9- MADD dual-sgRNA targeting Exon 3 of the human MADD gene. ( B ) Confirmation of MADD Knockout by PCR compared to control cells. ( C ) Western blot analysis of MADD expression in control and knockout cells after 24 h of treatment with 4-Hydroxytamoxifen (4HT). β-actin served as a loading control. ( D ) Immunocytochemistry of MADD expression. Cells were cultured on sterile coverslips in the 8-well chamber, and following fixation, the cells were stained with anti-MADD-specific antibodies. DAPI staining was used for counter-staining. (Green = MADD, blue = nucleus) absence of any green color indicates that MADD was successfully knocked out in ATC cells at the translational level.

    Article Snippet: Lipofectamine 3000 (Invitrogen, Carlsbad, CA, USA) and sgRNA 1&2 and Cas9 plasmid DNA were separately diluted in 250 μl of portions of Opti-MEM reduced serum medium (Invitrogen).

    Techniques: CRISPR, Knock-Out, Control, Western Blot, Expressing, Immunocytochemistry, Cell Culture, Sterility, Staining

    Journal: eLife

    Article Title: Single-cell eQTL mapping in yeast reveals a tradeoff between growth and reproduction

    doi: 10.7554/eLife.95566

    Figure Lengend Snippet:

    Article Snippet: Recombinant DNA reagent , p415 GalL-Cas9-Cyc1t (plasmid) , , RRID: Addgene_43804 , Gal inducible CAS9 with LEU cassette.

    Techniques: Recombinant, Plasmid Preparation, Marker, RNA Expression, Variant Assay, Software