Pub Date : 2024-12-18eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.001018
Grace Keirn, Cole A Kiser, Leon F Laskowski, Jordan Hensley, Rachel Mortan, Thuy Nguyen, Shallee T Page, Charles Du, Jeroen T F Gillard, Anya Goodman, James J Youngblom, Chinmay P Rele, Laura K Reed
Gene model for the ortholog of Ribosomal protein S6 kinase ( S6k ) in the Dyak_CAF1 Genome Assembly (GenBank Accession: GCA_000005975.1) of Drosophila yakuba . This ortholog was characterized as part of a developing dataset to study the evolution of the Insulin/insulin-like growth factor signaling pathway (IIS) across the genus Drosophila using the Genomics Education Partnership gene annotation protocol for Course-based Undergraduate Research Experiences.
{"title":"Gene model for the ortholog of <i>S6k</i> in <i>Drosophila yakuba</i>.","authors":"Grace Keirn, Cole A Kiser, Leon F Laskowski, Jordan Hensley, Rachel Mortan, Thuy Nguyen, Shallee T Page, Charles Du, Jeroen T F Gillard, Anya Goodman, James J Youngblom, Chinmay P Rele, Laura K Reed","doi":"10.17912/micropub.biology.001018","DOIUrl":"https://doi.org/10.17912/micropub.biology.001018","url":null,"abstract":"<p><p>Gene model for the ortholog of <i>Ribosomal protein S6 kinase</i> ( <i>S6k</i> ) in the Dyak_CAF1 Genome Assembly (GenBank Accession: GCA_000005975.1) of <i>Drosophila yakuba</i> . This ortholog was characterized as part of a developing dataset to study the evolution of the Insulin/insulin-like growth factor signaling pathway (IIS) across the genus <i>Drosophila</i> using the Genomics Education Partnership gene annotation protocol for Course-based Undergraduate Research Experiences.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11696350/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142934004","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-18eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.001413
Felipe L Teixeira, Heidi Pauer, Gabriel Luis C Valente, Geraldo Renato de Paula
Pseudomonas aeruginosa is an important pathogen associated with both chronic wounds and bloodstream infections. Virulence factors required for the establishment of acute and chronic infections differ substantially. Since bacteremia can be a severe outcome of wound colonization, we performed a comparative analysis of virulence between P. aeruginosa strains isolated from the bloodstream and chronic wounds. Our results show that, in general, P. aeruginosa strains isolated from bloodstream infections are more virulent than strains that colonize chronic wounds.
{"title":"Comparative analysis of virulence factors produced by <i>Pseudomonas aeruginosa</i> strains isolated from chronic wounds or bloodstream infections.","authors":"Felipe L Teixeira, Heidi Pauer, Gabriel Luis C Valente, Geraldo Renato de Paula","doi":"10.17912/micropub.biology.001413","DOIUrl":"10.17912/micropub.biology.001413","url":null,"abstract":"<p><p><i>Pseudomonas aeruginosa</i> is an important pathogen associated with both chronic wounds and bloodstream infections. Virulence factors required for the establishment of acute and chronic infections differ substantially. Since bacteremia can be a severe outcome of wound colonization, we performed a comparative analysis of virulence between <i>P. aeruginosa</i> strains isolated from the bloodstream and chronic wounds. Our results show that, in general, <i>P. aeruginosa</i> strains isolated from bloodstream infections are more virulent than strains that colonize chronic wounds.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11688615/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142924149","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-18eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.001392
Deepak Maurya, Bama Charan Mondal
Macrophages are present in various forms throughout metazoans and play conserved roles in phagocytosis, immunity, and tissue homeostasis. In Drosophila melanogaster' s larval hematopoietic organ, the lymph gland, transient caspase-mediated activation of caspase-activated DNase triggers the DNA damage response (DDR), which is crucial for macrophage-type cell differentiation. Here, we report that other Drosophila species having different-sized mature lymph glands show effector caspase activity and DDR similar to those in Drosophila melanogaster , indicating that the developmental mechanism regulating phagocytic macrophage differentiation is conserved in different species of Drosophila .
{"title":"Larval hematopoietic organs of multiple <i>Drosophila</i> species show effector caspase activity and DNA damage response.","authors":"Deepak Maurya, Bama Charan Mondal","doi":"10.17912/micropub.biology.001392","DOIUrl":"10.17912/micropub.biology.001392","url":null,"abstract":"<p><p>Macrophages are present in various forms throughout metazoans and play conserved roles in phagocytosis, immunity, and tissue homeostasis. In <i>Drosophila melanogaster'</i> s larval hematopoietic organ, the lymph gland, transient caspase-mediated activation of caspase-activated DNase triggers the DNA damage response (DDR), which is crucial for macrophage-type cell differentiation. Here, we report that other <i>Drosophila</i> species having different-sized mature lymph glands show effector caspase activity and DDR similar to those in <i>Drosophila melanogaster</i> , indicating that the developmental mechanism regulating phagocytic macrophage differentiation is conserved in different species of <i>Drosophila</i> .</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11696351/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142934005","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The reversal of phototaxis has been observed in a wide range of animal species. However, environmental chemicals that can cause a quick reversal of phototaxis have rarely been reported. Here we identified hypochlorous acid (HClO) as an inducer of phototactic reversal in Vargula hilgendorfii , also known as sea fireflies. This species shows innate photophobic swimming behavior away from light sources and 0.1% HClO triggers rapid positive phototactic responses, that is reversible upon washout. Phototactic assays using monochromatic light irradiation revealed the highest photophobic responses at 460 nm, while the HClO-induced photophilic responses were observed widely, even in UV light.
{"title":"Sudden phototactic reversal induced by hypochlorous acid exposure in the bioluminescent ostracod crustacean, <i>Vargula hilgendorfii.</i>","authors":"Kouki Sugitani, Reika Ohnishi, Daigo Inaoka, Hiroki Ono, Noritaka Hirohashi","doi":"10.17912/micropub.biology.001410","DOIUrl":"10.17912/micropub.biology.001410","url":null,"abstract":"<p><p>The reversal of phototaxis has been observed in a wide range of animal species. However, environmental chemicals that can cause a quick reversal of phototaxis have rarely been reported. Here we identified hypochlorous acid (HClO) as an inducer of phototactic reversal in <i>Vargula hilgendorfii</i> , also known as sea fireflies. This species shows innate photophobic swimming behavior away from light sources and 0.1% HClO triggers rapid positive phototactic responses, that is reversible upon washout. Phototactic assays using monochromatic light irradiation revealed the highest photophobic responses at 460 nm, while the HClO-induced photophilic responses were observed widely, even in UV light.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11688616/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142916632","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-14eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.001401
Vipaporn Phuntumart, Lucia Boulos, Bella Nunnally, Isabella Lima, John Motter, Olivia Sidoti, Sam Rutherford, Hsin-Ho Wei, Raymond Larsen, Jill H Zeilstra-Ryalls
We report the discovery and genome sequence of mycobacteriophage Eugenia, isolated from soil samples collected in Akron, OH. Eugenia is a double-stranded DNA virus with a genome size of 69,139 bp, featuring 104 predicted protein-encoding genes, with 32 of these genes assigned putative functions.
{"title":"Genome Sequence of the <i>Mycobacterium smegmatis</i> Bacteriophage Eugenia.","authors":"Vipaporn Phuntumart, Lucia Boulos, Bella Nunnally, Isabella Lima, John Motter, Olivia Sidoti, Sam Rutherford, Hsin-Ho Wei, Raymond Larsen, Jill H Zeilstra-Ryalls","doi":"10.17912/micropub.biology.001401","DOIUrl":"10.17912/micropub.biology.001401","url":null,"abstract":"<p><p>We report the discovery and genome sequence of mycobacteriophage Eugenia, isolated from soil samples collected in Akron, OH. Eugenia is a double-stranded DNA virus with a genome size of 69,139 bp, featuring 104 predicted protein-encoding genes, with 32 of these genes assigned putative functions.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11682537/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142904361","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-10eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.001428
Rupali Dabas, Alan Koh, David Carling, Nazila Kamaly, André E X Brown
Efficient delivery of sensitive nucleic acid payloads, including mRNA, in Caenorhabditis elegans remains challenging, especially with traditional, labor-intensive transgenesis methods. We addressed these challenges using polymeric nanogels (NGs) as an advanced platform for mRNA delivery in C. elegans . These polymeric delivery vehicles can be engineered to suit desired applications owing to their chemical versatility, resulting from the ability to conjugate multiple functional groups onto the same backbone. Here, we validate the in vivo RNA delivery potential of redox-responsive NGs. The NGs showed up to 72.4 % RNA encapsulation and 6.61 % loading efficiencies and facilitated the controlled release of the mRNA payloads at intracellular concentrations of the reducing agent glutathione, where most of the RNA was released within 24 hours. As a proof of concept, we successfully delivered green fluorescent protein (GFP)-expressing mRNA using NGs in C. elegans for the first time. Physicochemical characterization revealed uniform NG size and charge, and fluorescence microscopy confirmed GFP expression in the gut after 24 hours of treatment. Our findings show NGs' potential as an mRNA delivery system in C. elegans .
{"title":"Redox-Responsive Polymeric Nanogels as Efficient mRNA Delivery Vehicles in <i>Caenorhabditis elegans</i>.","authors":"Rupali Dabas, Alan Koh, David Carling, Nazila Kamaly, André E X Brown","doi":"10.17912/micropub.biology.001428","DOIUrl":"10.17912/micropub.biology.001428","url":null,"abstract":"<p><p>Efficient delivery of sensitive nucleic acid payloads, including mRNA, in <i>Caenorhabditis elegans</i> remains challenging, especially with traditional, labor-intensive transgenesis methods. We addressed these challenges using polymeric nanogels (NGs) as an advanced platform for mRNA delivery in <i>C. elegans</i> . These polymeric delivery vehicles can be engineered to suit desired applications owing to their chemical versatility, resulting from the ability to conjugate multiple functional groups onto the same backbone. Here, we validate the <i>in vivo</i> RNA delivery potential of redox-responsive NGs. The NGs showed up to 72.4 % RNA encapsulation and 6.61 % loading efficiencies and facilitated the controlled release of the mRNA payloads at intracellular concentrations of the reducing agent glutathione, where most of the RNA was released within 24 hours. As a proof of concept, we successfully delivered green fluorescent protein (GFP)-expressing mRNA using NGs in <i>C. elegans</i> for the first time. Physicochemical characterization revealed uniform NG size and charge, and fluorescence microscopy confirmed GFP expression in the gut after 24 hours of treatment. Our findings show NGs' potential as an mRNA delivery system in <i>C. elegans</i> .</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11669991/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142900759","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-08eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.001398
Hannah B Bonogafsky, Kelly M Freer, Taylor B Sanderson, Kira A Yost, Ayden J Pyle, Ginavieve Rowley, Maria D Gainey
Bacteriophage Evcara is a podovirus isolated on Microbacterium paraoxydans NRRL B-24275. Its genome is 16,285 bp in length and contains 22 predicted protein-coding genes. Evcara, has been assigned to cluster GI with Microbacteriumfoliorum phages PineapplePizza and Curie that share 10 homologues with the well-characterized Bacillus subtilis phage phi29.
{"title":"Complete annotated genome sequence of <i>Microbacterium paraoxydans</i> phage Evcara, a cluster GI podovirus isolated from compost.","authors":"Hannah B Bonogafsky, Kelly M Freer, Taylor B Sanderson, Kira A Yost, Ayden J Pyle, Ginavieve Rowley, Maria D Gainey","doi":"10.17912/micropub.biology.001398","DOIUrl":"10.17912/micropub.biology.001398","url":null,"abstract":"<p><p>Bacteriophage Evcara is a podovirus isolated on <i>Microbacterium paraoxydans</i> NRRL B-24275. Its genome is 16,285 bp in length and contains 22 predicted protein-coding genes. Evcara, has been assigned to cluster GI with <i>Microbacterium</i> <i>foliorum</i> phages PineapplePizza and Curie that share 10 homologues with the well-characterized <i>Bacillus subtilis</i> phage phi29.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11664425/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142883814","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-08eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.000853
Alyssa C Koehler, Emma Seay, Hannah Ewing, Zachary Mearse, Ana Maria Rocha de Almeida, Sara Cline, Jamie Siders, Lindsey J Long, Chinmay P Rele, Laura K Reed
Gene model for the ortholog of Downstream of raf1 ( Dsor1 ) in the May 2011 (Broad dper_caf1/DperCAF1) Genome Assembly (GenBank Accession: GCA_000005195.1 ) of Drosophila persimilis . This ortholog was characterized as part of a developing dataset to study the evolution of the Insulin/insulin-like growth factor signaling pathway (IIS) across the genus Drosophila using the Genomics Education Partnership gene annotation protocol for Course-based Undergraduate Research Experiences.
{"title":"Gene model for the ortholog of <i>Dsor1</i> in <i>Drosophila persimilis</i>.","authors":"Alyssa C Koehler, Emma Seay, Hannah Ewing, Zachary Mearse, Ana Maria Rocha de Almeida, Sara Cline, Jamie Siders, Lindsey J Long, Chinmay P Rele, Laura K Reed","doi":"10.17912/micropub.biology.000853","DOIUrl":"10.17912/micropub.biology.000853","url":null,"abstract":"<p><p>Gene model for the ortholog of Downstream of raf1 ( <i>Dsor1</i> ) in the May 2011 (Broad dper_caf1/DperCAF1) Genome Assembly (GenBank Accession: GCA_000005195.1 ) of <i>Drosophila persimilis</i> . This ortholog was characterized as part of a developing dataset to study the evolution of the Insulin/insulin-like growth factor signaling pathway (IIS) across the genus <i>Drosophila</i> using the Genomics Education Partnership gene annotation protocol for Course-based Undergraduate Research Experiences.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11664427/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142883819","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-08eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.000782
Megan E Lawson, Madeline McAbee, Rae A Lucas, Scott Tanner, Jacqueline Wittke-Thompson, Tara A Pelletier, Zeynep Ozsoy, Rachel Sterne-Marr, Chinmay P Rele, Laura K Reed
Gene model for the ortholog of Insulin-like peptide 5 ( Ilp5 ) in the D. ananassae May 2011 (Agencourt dana_caf1/DanaCAF1) Genome Assembly (GenBank Accession: GCA_000005115.1 ) of Drosophila ananassae . This ortholog was characterized as part of a developing dataset to study the evolution of the Insulin/insulin-like growth factor signaling pathway (IIS) across the genus Drosophila using the Genomics Education Partnership gene annotation protocol for Course-based Undergraduate Research Experiences.
{"title":"Gene model for the ortholog of <i>Ilp5</i> in <i>Drosophila ananassae</i>.","authors":"Megan E Lawson, Madeline McAbee, Rae A Lucas, Scott Tanner, Jacqueline Wittke-Thompson, Tara A Pelletier, Zeynep Ozsoy, Rachel Sterne-Marr, Chinmay P Rele, Laura K Reed","doi":"10.17912/micropub.biology.000782","DOIUrl":"10.17912/micropub.biology.000782","url":null,"abstract":"<p><p>Gene model for the ortholog of Insulin-like peptide 5 ( <i>Ilp5</i> ) in the <i>D. ananassae</i> May 2011 (Agencourt dana_caf1/DanaCAF1) Genome Assembly (GenBank Accession: GCA_000005115.1 ) of <i>Drosophila ananassae</i> . This ortholog was characterized as part of a developing dataset to study the evolution of the Insulin/insulin-like growth factor signaling pathway (IIS) across the genus <i>Drosophila</i> using the Genomics Education Partnership gene annotation protocol for Course-based Undergraduate Research Experiences.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11664428/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142883825","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-06eCollection Date: 2024-01-01DOI: 10.17912/micropub.biology.001275
Darrian Talamantes, Caitlin Kirkpatrick, Jason Wallace
Tall fescue ( Festuca arundinacea ) is a widely adopted forage and turf grass. This is partly due to a fungal endophyte, Epichloë coenophiala, which confers both abiotic and biotic stress tolerance. Although PCR primers exist to test for endophyte presence, these were not designed to quantitatively analyze the amount of fungus in the plant. In this study, we test different primer sets for quantitative biomass analysis of tall fescue and E. coenophiala. We report standard curves, r-squared, and efficiency values for every primer set and identify those most suited for qPCR in this system.
{"title":"Developing robust quantitative PCR primers for comparative biomass analysis of Tall Fescue (Festuca arundinacea) and its Epichloë endophyte.","authors":"Darrian Talamantes, Caitlin Kirkpatrick, Jason Wallace","doi":"10.17912/micropub.biology.001275","DOIUrl":"10.17912/micropub.biology.001275","url":null,"abstract":"<p><p>Tall fescue ( <i>Festuca arundinacea</i> ) is a widely adopted forage and turf grass. This is partly due to a fungal endophyte, <i>Epichloë coenophiala,</i> which confers both abiotic and biotic stress tolerance. Although PCR primers exist to test for endophyte presence, these were not designed to quantitatively analyze the amount of fungus in the plant. In this study, we test different primer sets for quantitative biomass analysis of tall fescue and <i>E. coenophiala.</i> We report standard curves, r-squared, and efficiency values for every primer set and identify those most suited for qPCR in this system.</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11663250/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142878928","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}