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  • 86
    Agilent technologies 180 000 feature
    180 000 Feature, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/180 000 feature/product/Agilent technologies
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    180 000 feature - by Bioz Stars, 2021-05
    86/100 stars
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    99
    Agilent technologies genome wide oligonucleotide cgh array
    Genome Wide Oligonucleotide Cgh Array, supplied by Agilent technologies, 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/genome wide oligonucleotide cgh array/product/Agilent technologies
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    genome wide oligonucleotide cgh array - by Bioz Stars, 2021-05
    99/100 stars
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    86
    Qiagen hiperfect
    Hiperfect, supplied by Qiagen, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/hiperfect/product/Qiagen
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    hiperfect - by Bioz Stars, 2021-05
    86/100 stars
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    86
    Qiagen negative control sirna
    p21 degradation is mediated by the CRL4 Cdt2 ligase complex. A ) Schematic illustrating the experimental protocol for <t>siRNA</t> knockdown of ligase components in Figures 1B and 1C . B and C ) p21 degradation requires DDB1 (B) and Cdt2 (C) . Murine <t>A9</t> cells were targeted with control siRNA or siRNA to DDB1 (B) or Cdt2 (C) as depicted in Figure 1A . Uninfected control cells were harvested at the time of release (Mock T0). Infections were done at the time of release at an MOI of 10 before harvest at 24 and 40 hr pi. Western blots were performed using antibodies against the indicated proteins.
    Negative Control Sirna, supplied by Qiagen, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/negative control sirna/product/Qiagen
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    negative control sirna - by Bioz Stars, 2021-05
    86/100 stars
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    Image Search Results


    p21 degradation is mediated by the CRL4 Cdt2 ligase complex. A ) Schematic illustrating the experimental protocol for siRNA knockdown of ligase components in Figures 1B and 1C . B and C ) p21 degradation requires DDB1 (B) and Cdt2 (C) . Murine A9 cells were targeted with control siRNA or siRNA to DDB1 (B) or Cdt2 (C) as depicted in Figure 1A . Uninfected control cells were harvested at the time of release (Mock T0). Infections were done at the time of release at an MOI of 10 before harvest at 24 and 40 hr pi. Western blots were performed using antibodies against the indicated proteins.

    Journal: PLoS Pathogens

    Article Title: Efficient Parvovirus Replication Requires CRL4Cdt2-Targeted Depletion of p21 to Prevent Its Inhibitory Interaction with PCNA

    doi: 10.1371/journal.ppat.1004055

    Figure Lengend Snippet: p21 degradation is mediated by the CRL4 Cdt2 ligase complex. A ) Schematic illustrating the experimental protocol for siRNA knockdown of ligase components in Figures 1B and 1C . B and C ) p21 degradation requires DDB1 (B) and Cdt2 (C) . Murine A9 cells were targeted with control siRNA or siRNA to DDB1 (B) or Cdt2 (C) as depicted in Figure 1A . Uninfected control cells were harvested at the time of release (Mock T0). Infections were done at the time of release at an MOI of 10 before harvest at 24 and 40 hr pi. Western blots were performed using antibodies against the indicated proteins.

    Article Snippet: RNA interference A9 cells were transfected twice with 40 nM Control siRNA (Qiagen #1022076), Cdt2 (DTL) siRNA (Dharmacon #L-045921-01-0005), Cul4A (Dharmacon #L-052208-00-0005) or DDB1 siRNA (Dharmacon #L-043146-01-0005). siRNA transfections were performed using HiPerfect (Qiagen).

    Techniques: Western Blot

    The CRL4 Cdt2 E3 ligase complex is important for MVM replication. A ) Schematic showing the experimental protocol for figures 2B and 2C . B and C ) Upper panels: murine A9 cells treated with siRNA as shown in 2A were infected at an MOI of 0.5, harvested at the indicated time points and processed for Southern blotting using an MVM genomic probe. Rf - replicative forms. SS - single stranded genomic DNA. Representative Southern Blots are shown; quantifications in the text reflect two DDB1 and three Cdt2 separate knockdown experiments. Lower panels: western blots show knockdown of DDB1 and Cdt2 done in parallel experiments under identical conditions to replication assays.

    Journal: PLoS Pathogens

    Article Title: Efficient Parvovirus Replication Requires CRL4Cdt2-Targeted Depletion of p21 to Prevent Its Inhibitory Interaction with PCNA

    doi: 10.1371/journal.ppat.1004055

    Figure Lengend Snippet: The CRL4 Cdt2 E3 ligase complex is important for MVM replication. A ) Schematic showing the experimental protocol for figures 2B and 2C . B and C ) Upper panels: murine A9 cells treated with siRNA as shown in 2A were infected at an MOI of 0.5, harvested at the indicated time points and processed for Southern blotting using an MVM genomic probe. Rf - replicative forms. SS - single stranded genomic DNA. Representative Southern Blots are shown; quantifications in the text reflect two DDB1 and three Cdt2 separate knockdown experiments. Lower panels: western blots show knockdown of DDB1 and Cdt2 done in parallel experiments under identical conditions to replication assays.

    Article Snippet: RNA interference A9 cells were transfected twice with 40 nM Control siRNA (Qiagen #1022076), Cdt2 (DTL) siRNA (Dharmacon #L-045921-01-0005), Cul4A (Dharmacon #L-052208-00-0005) or DDB1 siRNA (Dharmacon #L-043146-01-0005). siRNA transfections were performed using HiPerfect (Qiagen).

    Techniques: Infection, Southern Blot, Western Blot