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Promega magnesil pmps
Magnesil Pmps, 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/magnesil+pmps/magnesil+pmps/pm37624892-231-1-19
Average 90 stars, based on 1 article reviews
magnesil pmps - by Bioz Stars, 2026-09
90/100 stars

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Article Title: Efficient Sample Preparation from Complex Biological Samples Using a Sliding Lid for Immobilized Droplet Extractions
Article Snippet: For each experiment, 2 μL of Magnesil PMPs (#MD1471, Promega, Madison, WI) was added to each input solution of 40 μL.

DNA Extraction:

Article Title: Efficient Sample Preparation from Complex Biological Samples Using a Sliding Lid for Immobilized Droplet Extractions
Article Snippet: Samples were also run on an SDS-PAGE gel (NuPAGE 4–12% Bis-Tris Gel, Invitrogen) and silver stained (SilverQuest Silver Staining Kit, Invitrogen) to determine if GFP was effectively separated from the bulk of the nonfluorescent bacterial proteins. .. Samples to measure DNA extraction were prepared by lysing LNCaP cells in Buffer RLT (Qiagen) for 5 min at room temperature with 2 μL of MagneSil PMPs (Promega). ..

Quantitation Assay:

Article Title: Distinctiveness of declining northern populations of Blanchard’s Cricket Frog (Acris blanchardi) justifies recovery efforts
Article Snippet: Peripheral populations of widespread species are often considered unworthy of conservation efforts; however, they may be adapted to the conditions found at the range edge and are therefore important to the future evolutionary potential of the species.. Blanchard’s Cricket Frog (Acris blanchardi Harper, 1947) is widespread and abundant throughout the central United States, but is declining at the northern edge of its range.. To assess the distinctiveness and conservation value of the northern populations, we investigated the spatial genetic structure and phylogeography of this anuran using mitochondrial control region sequences.



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(a) Photograph of the microfluidic device with chambers filled with food dye for easy visualization, containing the following: (A) sample chamber, containing <t>superparamagnetic</t> particles (PMPs) as indicated by I; (B–D) wash chambers; (E) DNA amplification chamber; (F) positive control chamber; and (G) negative control chamber. Each chamber contains 1 or 2 access holes (1 mm diameter) as shown by H as an example; (b) photograph of the PMMA mold showing negative features of the above microfluidic device design
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(a) Photograph of the microfluidic device with chambers filled with food dye for easy visualization, containing the following: (A) sample chamber, containing <t>superparamagnetic</t> particles (PMPs) as indicated by I; (B–D) wash chambers; (E) DNA amplification chamber; (F) positive control chamber; and (G) negative control chamber. Each chamber contains 1 or 2 access holes (1 mm diameter) as shown by H as an example; (b) photograph of the PMMA mold showing negative features of the above microfluidic device design
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(a) Photograph of the microfluidic device with chambers filled with food dye for easy visualization, containing the following: (A) sample chamber, containing <t>superparamagnetic</t> particles (PMPs) as indicated by I; (B–D) wash chambers; (E) DNA amplification chamber; (F) positive control chamber; and (G) negative control chamber. Each chamber contains 1 or 2 access holes (1 mm diameter) as shown by H as an example; (b) photograph of the PMMA mold showing negative features of the above microfluidic device design
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(a) Photograph of the microfluidic device with chambers filled with food dye for easy visualization, containing the following: (A) sample chamber, containing superparamagnetic particles (PMPs) as indicated by I; (B–D) wash chambers; (E) DNA amplification chamber; (F) positive control chamber; and (G) negative control chamber. Each chamber contains 1 or 2 access holes (1 mm diameter) as shown by H as an example; (b) photograph of the PMMA mold showing negative features of the above microfluidic device design

Journal: Ecology and Evolution

Article Title: On‐site genetic analysis for species identification using lab‐on‐a‐chip

doi: 10.1002/ece3.7053

Figure Lengend Snippet: (a) Photograph of the microfluidic device with chambers filled with food dye for easy visualization, containing the following: (A) sample chamber, containing superparamagnetic particles (PMPs) as indicated by I; (B–D) wash chambers; (E) DNA amplification chamber; (F) positive control chamber; and (G) negative control chamber. Each chamber contains 1 or 2 access holes (1 mm diameter) as shown by H as an example; (b) photograph of the PMMA mold showing negative features of the above microfluidic device design

Article Snippet: A 500‐μl aliquot was then injected into the main sample chamber along with 1 μl of superparamagnetic particles (MagneSil PMPs (Promega, UK)).

Techniques: DNA Amplification, Positive Control, Negative Control