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Name Authors DOI Group Summary Associated Publications RRIDs used Affiliations External URL Version Publication Date Proper Citation Record Last Update
ProteSEEKER™
 
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G-Biosciences DOI:10.17504/protocols.io.e5fbg3n G-Biosciences This protocol is for the ProteSEEKER™ kit, designed to identify the specific type of proteases present in cell or tissue lysates, and allows determining the minimal number of individual protease inhibitors required for a sample.  https://www.gbiosciences.com/image/pdfs/protocol/786-325_protocol.pdf 1 2017 G-Biosciences 2017. ProteSEEKER™. protocols.io https://dx.doi.org/10.17504/protocols.io.e5fbg3n 2021-04-15 09:14:29
SmartSeq2 for HTP Generation of Bulk RNA Libraries- with Pipetting plan
 
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Sasa T, Matjaž H DOI:10.17504/protocols.io.7f2hjqe [insert abstract from MACA_Bulk paper] BioSistemika, BioSistemika 5 2019 Sasa T, Matjaž H 2019. SmartSeq2 for HTP Generation of Bulk RNA Libraries- with Pipetting plan . protocols.io https://dx.doi.org/10.17504/protocols.io.7f2hjqe 2021-04-15 09:14:23
PCR Protocol for TaqMan® Genotyping Assays
 
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Eyleen Nabyla Alvarenga Niitsuma, Gabriel da Rocha Fernandes, Francisco Carlos Félix Lana DOI:10.17504/protocols.io.sfzebp6 Niitsuma ENA, Fernandes GdR, Lana FCF (2018) The TLR1 gene is associated with higher protection from leprosy in women. PLoS ONE 13(10): e0205234. doi: 10.1371/journal.pone.0205234 Instituto Federal de Educação, Ciência e Tecnologia do Norte de Minas Gerais, Instituto René Rachou - Fiocruz Minas, Departamento de Enfermagem Materno-infantil e Saúde Pública, Escola de Enfermagem, Universidade Federal de Minas Gerais - UFMG https://doi.org/10.1371/journal.pone.0205234 1 2018 Eyleen Nabyla Alvarenga Niitsuma, Gabriel da Rocha Fernandes, Francisco Carlos Félix Lana 2018. PCR Protocol for TaqMan® Genotyping Assays. protocols.io https://dx.doi.org/10.17504/protocols.io.sfzebp6 2021-04-15 09:14:28
Less invasive surfactant administration in preterm neonates with respiratory distress syndrome: a network meta-analysis
 
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Ioannis Bellos, Georgia Fitrou, Aakash Pandita DOI:10.17504/protocols.io.bcbmisk6 Preterm birth is often associated with respiratory distress syndrome, which may lead to bronchopulmonary dysplasia and high rates of morbidity and mortality. The current treatment approach is the initial use of nasal continuous positive airway pressure (nCPAP), followed by surfactant administration in neonates with worsening respiratory distress. The aim of the present network meta-analysis is to simultaneously assess the effects of less invasive methods for administering surfactant on clinical outcomes and compare them to the conventional InSurE (Intubation, Surfactant administration and Extubation) method. National and Kapodistrian University of Athens, Greece, National and Kapodistrian University of Athens, Greece, Department of Neonatology, Sanjay Gandhi PGIMS, Lucknow, U.P, India 1 2020 Ioannis Bellos, Georgia Fitrou, Aakash Pandita 2020. Less invasive surfactant administration in preterm neonates with respiratory distress syndrome: a network meta-analysis. protocols.io https://dx.doi.org/10.17504/protocols.io.bcbmisk6 2021-04-15 09:14:28
LB Media
 
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William Brydon, Sricharan Kadimi DOI:10.17504/protocols.io.3idgka6 UConn iGEM LB (Luria-Bertani) media is commonly used for bacterial culture. We use it for overnight cultures after transformations. University of Connecticut, University of Connecticut 1 2019 William Brydon, Sricharan Kadimi 2019. LB Media. protocols.io https://dx.doi.org/10.17504/protocols.io.3idgka6 2021-04-15 09:14:28
Immunohistochemical labelling of spinal cord neurons involved in bladder activity
 
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Janet Keast, Peregrine Osborne, Nicole Wiedmann DOI:10.17504/protocols.io.bakkicuw SPARC This protocol is used for immunohistochemical visualisation of immediate early gene expression (c-Fos or Egr-1) in cryosections of rat lumbosacral spinal cord. Free-floating sections are processed in a double labelling protocol to distinguish immediate early gene expression in different neurochemical classes of spinal cord neurons:ChAT [choline acetyltransferase]: preganglionic neuronsTH [tyrosine hydroxyls]: dopaminergic neuronsPax2: inhibitory interneurons RRID:AB_10609634
RRID:AB_2533990
RRID:AB_2097174
RRID:AB_390204
RRID:AB_11214092
University of Melbourne, University of Melbourne, University of Melbourne 1 2020 Janet Keast, Peregrine Osborne, Nicole Wiedmann 2020. Immunohistochemical labelling of spinal cord neurons involved in bladder activity. protocols.io https://dx.doi.org/10.17504/protocols.io.bakkicuw 2021-04-15 09:14:24
PMN- 05 Culture of Human PMN - IL-8 production
 
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Marco Cosentino, Elisa Storelli, Alessandra Luini, Massimiliano Legnaro, Emanuela Rasini, Marco Ferrari, Franca Marino DOI:10.17504/protocols.io.bhdgj23w Adrenergic Modulation of Migration, CD11b and CD18 Expression, ROS and interleukin-8 Production by Human Polymorphonuclear Leukocytes.Angela Scanzano, Laura Schembri, Emanuela Rasini, Alessandra Luini, Jessica Dallatorre, Massimiliano Legnaro, Raffaella Bombelli, Terenzio Congiu, Marco Cosentino, Franca Marino. Inflamm Res. 2015 Feb;64(2):127-35. doi: 10.1007/s00011-014-0791-8. Epub 2015 Jan 6. Center for Research in Medical Pharmacology, University of Insubria (Varese, Italy), Center for Research in Medical Pharmacology, University of Insubria (Varese, Italy), Center for Research in Medical Pharmacology, University of Insubria (Varese, Italy), Center for Research in Medical Pharmacology, University of Insubria (Varese, Italy), Center for Research in Medical Pharmacology, University of Insubria (Varese, Italy), Center for Research in Medical Pharmacology, University of Insubria (Varese, Italy), Center for Research in Medical Pharmacology, University of Insubria (Varese, Italy) 1 2020 Marco Cosentino, Elisa Storelli, Alessandra Luini, Massimiliano Legnaro, Emanuela Rasini, Marco Ferrari, Franca Marino 2020. PMN- 05 Culture of Human PMN - IL-8 production. protocols.io https://dx.doi.org/10.17504/protocols.io.bhdgj23w 2021-04-15 09:14:23
Isolation of phosphoproteins from symbiotic and aposymbiotic Aiptasia anemones for elucidation of the phosphoproteome
 
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Fabia Simona, Huoming Zhang, Christian Voolstra DOI:10.17504/protocols.io.txuepnw reefgenomics, Aiptasia-Symbiodiniaceae Model System The analysis of gene expression data via RNA sequencing (RNA-Seq) has become a standard method for model and non-model organisms to identify genes of interest associated with a specific stressor of physiological state. More recently, mass spectrometry (MS)-based proteomics started to become a standard method to assay the phenotype of an organism via means of its expressed proteins. MS has also become the method of choice for the study of protein phosphorylation. Phosphoproteomics targets proteins that are subjected to phosphorylation via means of their serine, threonine, and tyrosine residues. Phosphorylation is a reversible modification that plays a key role in controlling the activity of proteins as well as their function and subcellular localization.To bring MS-based phosphoproteomics to the emerging coral model system Aiptasia, we developed a protocol for phosphosphproteins extraction and generation of a phosphoproteome assay (spectral) library, a comprehensive non-redundant collection of Aiptasia phosphoproteins. Based on the assay library, we then performed accurate label-free quantification (by DIA/SWATH-MS) of the Aiptasia phosphoproteome. Our method reproducibly identifies and quantifies a broad fraction of the phosphorylated proteome of Aiptasia and is comparable to methods developed for other model systems Red Sea Research Center, Division of Biological and Environmental Science and Engineering, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia, Bioscience Core Laboratory, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia., Red Sea Research Center, Division of Biological and Environmental Science and Engineering, King Abdullah University of Science and Technology, Thuwal, Saudi Arabia 2 2018 Fabia Simona, Huoming Zhang, Christian Voolstra 2018. Isolation of phosphoproteins from symbiotic and aposymbiotic Aiptasia anemones for elucidation of the phosphoproteome. protocols.io https://dx.doi.org/10.17504/protocols.io.txuepnw 2021-04-15 09:14:27
Script P5: Diversity
 
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HANNIGAN GD, GRICE EA, ET AL. DOI:10.17504/protocols.io.efrbbm6 VERVE Net, Club Grice This protocol provides a method to predict phage community diversity using the algorithm PHACCS. Sequencing of viral communities often results in a high percent of unknown reads, largely due to our incomplete reference databases. To address this unknown factor of viromes, the algorithm PHACCS (PHAge Communities from Contig Spectra) was developed to predict virus community alpha diversity without the use of taxonomic references. Based on the methods from the following publication:Hannigan, Geoffrey D., et al. "The Human Skin Double-Stranded DNA Virome: Topographical and Temporal Diversity, Genetic Enrichment, and Dynamic Associations with the Host Microbiome." mBio 6.5 (2015): e01578-15. Kindler L, Stoliartchouk A, Teytelman L, Hurwitz BL, Method-centered digital communities on protocols.io for fast-paced scientific innovation. F1000Research doi: 10.12688/f1000research.9453.2 Grice Lab, DEPARTMENT OF DERMATOLOGY UNIVERSITY OF PENNSYLVANIA, Grice Lab, DEPARTMENT OF DERMATOLOGY UNIVERSITY OF PENNSYLVANIA, Grice Lab, DEPARTMENT OF DERMATOLOGY UNIVERSITY OF PENNSYLVANIA http://mbio.asm.org/content/6/5/e01578-15.full 1 2016 HANNIGAN GD, GRICE EA, ET AL. 2016. Script P5: Diversity. protocols.io https://dx.doi.org/10.17504/protocols.io.efrbbm6 2021-04-15 09:14:29
How to prepare zebrafish brain tissue samples for biochemical assays
 
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Adrieli Sachett, Matheus Gallas-Lopes, Radharani , Greicy M M Conterato, Ana Herrmann, Angelo Piato DOI:10.17504/protocols.io.bjkdkks6 Fish behavior and physiology Zebrafish are increasingly used as a model animal in neuroscience research. Here we describe our protocol to collect and process zebrafish brains so they are well presearved and viable for biochemical assays. Universidade Federal do Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Universidade Federal do Rio Grande do Sul, Universidade Federal de Santa Catarina, Universidade Federal do Rio Grande do Sul, Universidade Federal do Rio Grande do Sul 1 2020 Adrieli Sachett, Matheus Gallas-Lopes, Radharani , Greicy M M Conterato, Ana Herrmann, Angelo Piato 2020. How to prepare zebrafish brain tissue samples for biochemical assays. protocols.io https://dx.doi.org/10.17504/protocols.io.bjkdkks6 2021-04-15 09:14:25
Determination of minimum inhibitory concentration values (MICs) against Sporothrix brasiliensis and Sporothrix schenckii
 
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luanaborba DOI:10.17504/protocols.io.bjgxkjxn L. P. Borba-Santos Borba-Santos LP, Vila T, Rozental S (2020) Identification of two potential inhibitors of Sporothrix brasiliensis and Sporothrix schenckii in the Pathogen Box collection. PLoS ONE 15(10): e0240658. doi: 10.1371/journal.pone.0240658 Universidade Federal do Rio de Janeiro https://doi.org/10.1371/journal.pone.0240658 2 2020 luanaborba 2020. Determination of minimum inhibitory concentration values (MICs) against Sporothrix brasiliensis and Sporothrix schenckii. protocols.io https://dx.doi.org/10.17504/protocols.io.bjgxkjxn 2021-04-15 09:14:23
BSCI:414--Lab 4 Plate Setup for COVID RT-qPCR
 
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Harley King USG Fall 2020 BSCI:414 LuminUltra 1 2020 Harley King 2020. BSCI:414--Lab 4 Plate Setup for COVID RT-qPCR. protocols.io https:// 2021-04-15 09:14:27
Manual setting of k-mer coverage peaks
 
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Afiahayati, Sato K, Namiki T, Hachiya T, Tanaka H, Sakakibara Y. DOI:10.17504/protocols.io.d7k9kv VERVE Net, Hurwitz Lab Contrary to single-genome assemblers (e.g., Velvet and SOAPdenovo), MetaVelvet assumes metagenomics settings. Accordingly, k-mer coverage histogram might be multi-modal rather than uni-modal. Please note that the coverage peak parameters can largely affect MetaVelvet assembling results. Although simple and automatic peak detection algorithm is implemented in meta-velvetg, we strongly recommend manual inspection of k-mer coverage peaks and manual setting of the coverage peak parameters. For manually setting the coverage peak parameters, please execute the following procedures. Sakakibara Lab, Sakakibara Lab, Sakakibara Lab, Sakakibara Lab, Sakakibara Lab, Sakakibara Lab http://metavelvet.dna.bio.keio.ac.jp/MV.html 1 2016 Afiahayati, Sato K, Namiki T, Hachiya T, Tanaka H, Sakakibara Y. 2016. Manual setting of k-mer coverage peaks. protocols.io https://dx.doi.org/10.17504/protocols.io.d7k9kv 2021-04-15 09:14:25
How to set up a protocol hackathon for your team
 
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Anita Broellochs, protocols.io Ambassadors DOI:10.17504/protocols.io.bgf8jtrw protocols.io Ambassadors Communicate and collaborate effectively with protocols.io. Research data and protocols will never leave the team, even if a person does. With protocols.io it is fast and easy to find the information that you want— a central place for all of your scientific data.If your team is planning to start using protocols.io, a protocol hackathon is a great way to get everyone on board. Protocol hackathons are fun as the entire team works on getting their protocols up on protocols.io at the same time rather than every team member trying to enter protocols one at the time by themselves.A protocol hackathon can take place remotely or in person. This protocol gives you a great overview of how you can go about setting up a protocol entry session (hackathon) for your team. protocols.io, protocols.io 3 2020 Anita Broellochs, protocols.io Ambassadors 2020. How to set up a protocol hackathon for your team. protocols.io https://dx.doi.org/10.17504/protocols.io.bgf8jtrw 2021-04-15 09:14:29
SIngle-strand library protocol adapter barcodes
 
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Tomasz Suchan W. Szafer Institute of Botany, Polish Academy of Sciences 1 2020 Tomasz Suchan 2020. SIngle-strand library protocol adapter barcodes. protocols.io https:// 2021-04-15 09:14:27
Density Gradient Fractionation of RNA from RNA-SIP Experiments
 
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Julie Huber, Caroline Fortunato DOI:10.17504/protocols.io.iu2ceye Center for Dark Energy Biosphere Investigations, Huber Lab, Chemistry Method Development Community This protocol is following RNA-SIP experiments and RNA extraction to fractionate the RNA according to density. The protocol is based on Leuders et al. 2010. WHOI, WHOI 3 2017 Julie Huber, Caroline Fortunato 2017. Density Gradient Fractionation of RNA from RNA-SIP Experiments. protocols.io https://dx.doi.org/10.17504/protocols.io.iu2ceye 2021-04-15 09:14:25
Loop L2 (even level) type IIS cloning - pCs-ye vectors
 
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Eftychis Frangedakis, Susana Sauret-Gueto, Anthony West, Marta Tomaselli, Nicola Patron, Marius Rebmann, Jim Haseloff DOI:10.17504/protocols.io.4wcgxaw OpenPlant Project Protocol based onPollak B, Cerda A, Delmans M, et al (2019) Loop assembly: a simple and open system for recursive fabrication of DNA circuits. New Phytol 222:628–640https://doi.org/10.1111/nph.15625 University of Cambridge, Plant Sciences, University of Cambridge, OpenPlant, Plant Sciences, University of Cambridge, OpenPlant, University of Cambridge, Open Plant, Plant Sciences, University of Cambridge, OpenPlant, Plant Sciences, University of Cambridge, OpenPlant, Plant Sciences, University of Cambridge, OpenPlant 1 2019 Eftychis Frangedakis, Susana Sauret-Gueto, Anthony West, Marta Tomaselli, Nicola Patron, Marius Rebmann, Jim Haseloff 2019. Loop L2 (even level) type IIS cloning - pCs-ye vectors. protocols.io https://dx.doi.org/10.17504/protocols.io.4wcgxaw 2021-04-15 09:14:23
Collection of Protocols and Guidelines for Phase 3 study of Vaccine Candidate for COVID-19
 
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Chris Ockenhouse, Chris Gast, Renee Holt, Jorge Flores DOI:10.17504/protocols.io.bj5pkq5n Coronavirus Method Development Community This is a collection of protocols for: "Phase 3 randomized, double-blinded, placebo-controlled trial to evaluate the safety, immunogenicity, and efficacy of Vaccine Candidate against COVID-19 in adults > 18 years of age"This generic Phase 3 protocol was developed by the PATH team with support of the Bill and Melinda Gates Foundation. The aim of the collection is to share recommended best practices in designing and implementing a Phase 3 study of a COVID-19 vaccine candidate. As Phase 3 trials of different Vaccine Candidates proceed around the world, following the same protocols will ensure consistency and comparability of the Phase 3 trial results.Please note that this is an evolving document, to be versioned and updated, based on community feedback and new data. Center for Vaccine Innovation and Access, PATH (Washington D.C. and Seattle, Washington), Center for Vaccine Innovation and Access, PATH (Washington D.C. and Seattle, Washington), Center for Vaccine Innovation and Access, PATH (Washington D.C. and Seattle, Washington), Center for Vaccine Innovation and Access, PATH (Washington D.C. and Seattle, Washington) 1 2020 Chris Ockenhouse, Chris Gast, Renee Holt, Jorge Flores 2020. Collection of Protocols and Guidelines for Phase 3 study of Vaccine Candidate for COVID-19. protocols.io https://dx.doi.org/10.17504/protocols.io.bj5pkq5n 2021-04-15 09:14:25
Sample run SOP for ECD/FID/TCD
 
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Sparky Jr. PDI Test USDA 1 2021 Sparky Jr. 2021. Sample run SOP for ECD/FID/TCD. protocols.io https:// 2021-04-15 09:14:23
In vitro Transcription assay for cyanobacterial DNA-dependent RNA Polymerase
 
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Lutz Berwanger DOI:10.17504/protocols.io.mpvc5n6 Axmann Lab, CyanoWorld In vitro transcriptions assay for cyanobacterial RNA polymerase. This protocol can be used either to do an in vitro transcription with small DNA fragments with desired promoter region or to use it with a promoter region integrated in a plasmid. Heinrich-Heine Universität Düsseldorf 2 2018 Lutz Berwanger 2018. In vitro Transcription assay for cyanobacterial DNA-dependent RNA Polymerase. protocols.io https://dx.doi.org/10.17504/protocols.io.mpvc5n6 2021-04-15 09:14:24

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