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Promega str profiling promega powerplex 16 system
Str Profiling Promega Powerplex 16 System, 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/promega+powerplex+16/promega+powerplex+16/pmc12209829-214-14-14
Average 90 stars, based on 1 article reviews
str profiling promega powerplex 16 system - by Bioz Stars, 2026-10
90/100 stars

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other:

Article Title: The utility of polyester and cotton as swabbing substrates for the removal of cellular material from surfaces.
Article Snippet: Various types of cotton and polyester fabrics were tested to ascertain the optimal physical and chemical characteristics of fabrics needed for the removal of cellular material from surfaces.. DNA quantitation values obtained on dried saliva stains showed no difference between cotton and polyester across all constructions and solvent conditions.. Fabrics used dry and with water yielded higher quantitation values than those used with isopropanol.

Polymerase Chain Reaction:

Article Title: Direct PCR amplification of forensic touch and other challenging DNA samples: A review.
Article Snippet: DNA evidence sample processing typically involves DNA extraction, quantification, and STR amplification; however, DNA loss can occur at both the DNA extraction and quantification steps, which is not ideal for forensic evidence containing low levels of DNA.. Direct PCR amplification of forensic unknown samples has been suggested as a means to circumvent extraction and quantification, thereby retaining the DNA typically lost during those procedures.. Direct PCR amplification is a method in which a sample is added directly to an amplification reaction without being subjected to prior DNA extraction, purification, or quantification.

Second Generation Multiplex Plus:

Article Title: Direct PCR amplification of forensic touch and other challenging DNA samples: A review.
Article Snippet: DNA evidence sample processing typically involves DNA extraction, quantification, and STR amplification; however, DNA loss can occur at both the DNA extraction and quantification steps, which is not ideal for forensic evidence containing low levels of DNA.. Direct PCR amplification of forensic unknown samples has been suggested as a means to circumvent extraction and quantification, thereby retaining the DNA typically lost during those procedures.. Direct PCR amplification is a method in which a sample is added directly to an amplification reaction without being subjected to prior DNA extraction, purification, or quantification.

Concentration Assay:

Article Title: Direct PCR amplification of forensic touch and other challenging DNA samples: A review.
Article Snippet: DNA evidence sample processing typically involves DNA extraction, quantification, and STR amplification; however, DNA loss can occur at both the DNA extraction and quantification steps, which is not ideal for forensic evidence containing low levels of DNA.. Direct PCR amplification of forensic unknown samples has been suggested as a means to circumvent extraction and quantification, thereby retaining the DNA typically lost during those procedures.. Direct PCR amplification is a method in which a sample is added directly to an amplification reaction without being subjected to prior DNA extraction, purification, or quantification.

Multiplex Assay:

Article Title: Multiplex_QA: an exploratory quality assessment tool for multiplexed electrophoretic assays.
Article Snippet: Multiplex_QA is a data analysis tool for visualizing shortand long-term changes in the performance of multiplexed electrophoretic assays, particularly the commercial short tandem repeat (STR) kits used by the human forensic identity community.. A number of quality metrics are calculated from the signal collected for the internal size standard included in nearly all multiplex assays.. These quality metrics are related to the signal intensity, symmetry, retention, resolution, and noise of data collected by capillary electrophoresis systems.



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Characterization and validation.

Journal: Stem cell research

Article Title: Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donor

doi: 10.1016/j.scr.2023.103280

Figure Lengend Snippet: Characterization and validation.

Article Snippet: Identity , STR analysis , STR polymorphisms for 15 loci plus amelogenin (Promega PowerPlex ® 16) match PBMCs , , Available with the authors.

Techniques: Biomarker Discovery, Immunocytochemistry, Labeling, Expressing, Mutagenesis, Virus, Immunofluorescence