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genomic dna from each sample and of pooled commercial reference  (Promega)

 
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    Structured Review

    Promega genomic dna from each sample and of pooled commercial reference
    Genomic Dna From Each Sample And Of Pooled Commercial Reference, supplied by Promega, 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/pooled+reference+sample/reference+genomic+dna/pm28841710-71-7-16
    Average 90 stars, based on 1 article reviews
    genomic dna from each sample and of pooled commercial reference - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Hybridization:

    Article Title: Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing
    Article Snippet: DNAs were extracted using Qiagen micro kits (Qiagen Valencia, CA). .. For hybridization, 100 ng of genomic DNA from each sample and of pooled commercial 46XX reference (Promega) were amplified using the GenomiPhi amplification kit (G.E. ..

    Article Title: Mesenchymal-like pancreatic cancer cells harbor specific genomic alterations more frequently than their epithelial-like counterparts
    Article Snippet: Comparative genomic hybridization (CGH) DNAs were extracted using Qiagen micro kits (Qiagen, Valencia, CA). .. For each hybridization, 1 μg of genomic DNA from each sample and 1 μg of pooled commercial 46XX reference DNA (Promega Corp., Madison, WI) were digested with DNaseI and labeled with Cy‐5 dUTP and Cy‐3 dUTP, respectively, using a BioPrime labeling kit (Invitrogen). .. All labeling reactions were assessed using a Nanodrop assay (Nanodrop, Wilmington, DE).

    Article Title: Advancing a clinically relevant perspective of the clonal nature of cancer
    Article Snippet: DNAs were extracted using Qiagen micro kits. .. For each hybridization, 100 ng of genomic DNA from each sample and of pooled commercial 46 , XX reference (Promega) were amplified using the GenomiPhi amplification kit (GE Healthcare). .. Subsequently, 1 μg of amplified sample and 1 μg of amplified reference template were digested with DNaseI and then labeled with Cy-5 dUTP and Cy-3 dUTP, respectively, using a BioPrime labeling kit (Invitrogen).

    Article Title: Clinical study of genomic drivers in pancreatic ductal adenocarcinoma
    Article Snippet: DNAs were extracted using Qiagen micro kits (Qiagen, Valencia, CA, USA). .. For each hybridisation 100 ng of genomic DNA from each sample and of pooled commercial 46XX reference (Promega, Madison, WI, USA) were amplified using the GenomiPhi amplification kit (GE Healthcare, Piscataway, NJ, USA). .. Subsequently 1 μg of amplified sample and 1μg of amplified reference template were digested with DNaseI then labelled with Cy-5 dUTP and Cy-3 dUTP respectively, using a BioPrime labelling kit (Invitrogen, Carlsbad, CA, USA).

    Article Title: A phase 2 trial of personalized cytotoxic therapy based on tumor immunohistochemistry in previously treated metastatic pancreatic cancer patients
    Article Snippet: DNA was extracted from each sorted sample using Qiagen micro kits (Qiagen Valencia, CA, USA). .. For each hybridization 100 ng of genomic DNA from each sample and of pooled commercial 46XX reference (Promega) were amplified using the GenomiPhi amplification kit (G.E. ..

    Article Title: Theoretical Analysis of Gas Breakdown Characteristic through a Narrow Discharge Tube
    Article Snippet: It is widely accepted that many cancers arise as a result of an acquired genomic instability and the subsequent evolution of tumor cells with variable patterns of selected and background aberrations.. The presence and behaviors of distinct neoplastic cell populations within a patient’s tumor may underlie multiple clinical phenotypes in cancers.. A goal of many current cancer genome studies is the identification of recurring selected driver events that can be advanced for the development of personalized therapies.

    Amplification:

    Article Title: Genome-Wide Characterization of Pancreatic Adenocarcinoma Patients Using Next Generation Sequencing
    Article Snippet: DNAs were extracted using Qiagen micro kits (Qiagen Valencia, CA). .. For hybridization, 100 ng of genomic DNA from each sample and of pooled commercial 46XX reference (Promega) were amplified using the GenomiPhi amplification kit (G.E. ..

    Article Title: Advancing a clinically relevant perspective of the clonal nature of cancer
    Article Snippet: DNAs were extracted using Qiagen micro kits. .. For each hybridization, 100 ng of genomic DNA from each sample and of pooled commercial 46 , XX reference (Promega) were amplified using the GenomiPhi amplification kit (GE Healthcare). .. Subsequently, 1 μg of amplified sample and 1 μg of amplified reference template were digested with DNaseI and then labeled with Cy-5 dUTP and Cy-3 dUTP, respectively, using a BioPrime labeling kit (Invitrogen).

    Article Title: Clinical study of genomic drivers in pancreatic ductal adenocarcinoma
    Article Snippet: DNAs were extracted using Qiagen micro kits (Qiagen, Valencia, CA, USA). .. For each hybridisation 100 ng of genomic DNA from each sample and of pooled commercial 46XX reference (Promega, Madison, WI, USA) were amplified using the GenomiPhi amplification kit (GE Healthcare, Piscataway, NJ, USA). .. Subsequently 1 μg of amplified sample and 1μg of amplified reference template were digested with DNaseI then labelled with Cy-5 dUTP and Cy-3 dUTP respectively, using a BioPrime labelling kit (Invitrogen, Carlsbad, CA, USA).

    Article Title: A phase 2 trial of personalized cytotoxic therapy based on tumor immunohistochemistry in previously treated metastatic pancreatic cancer patients
    Article Snippet: DNA was extracted from each sorted sample using Qiagen micro kits (Qiagen Valencia, CA, USA). .. For each hybridization 100 ng of genomic DNA from each sample and of pooled commercial 46XX reference (Promega) were amplified using the GenomiPhi amplification kit (G.E. ..

    Article Title: Theoretical Analysis of Gas Breakdown Characteristic through a Narrow Discharge Tube
    Article Snippet: It is widely accepted that many cancers arise as a result of an acquired genomic instability and the subsequent evolution of tumor cells with variable patterns of selected and background aberrations.. The presence and behaviors of distinct neoplastic cell populations within a patient’s tumor may underlie multiple clinical phenotypes in cancers.. A goal of many current cancer genome studies is the identification of recurring selected driver events that can be advanced for the development of personalized therapies.

    Labeling:

    Article Title: Mesenchymal-like pancreatic cancer cells harbor specific genomic alterations more frequently than their epithelial-like counterparts
    Article Snippet: Comparative genomic hybridization (CGH) DNAs were extracted using Qiagen micro kits (Qiagen, Valencia, CA). .. For each hybridization, 1 μg of genomic DNA from each sample and 1 μg of pooled commercial 46XX reference DNA (Promega Corp., Madison, WI) were digested with DNaseI and labeled with Cy‐5 dUTP and Cy‐3 dUTP, respectively, using a BioPrime labeling kit (Invitrogen). .. All labeling reactions were assessed using a Nanodrop assay (Nanodrop, Wilmington, DE).



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