The bacterial strains and plasmids used in this study are described in Table 2 . Oligonucleotides were purchased from Integrated DNA Technologies and are listed in Table 3 . Genomic DNA was isolated using the Qiagen 100/G genomic tip (Qiagen). Weakening of the staphylococcal cell wall required the addition of 100 µg of lysostaphin (Ambi) into the lysis buffer and incubation at 37°C for 30 min. Plasmids and PCR products were isolated using the Wizard plus kits (Promega), with T4 DNA ligase also purchased from Promega. Plasmids were isolated from staphylococci as described previously (3 (link)). Restriction enzymes, T4 DNA polymerase, and Phusion DNA polymerase were purchased from New England Biolabs. Phire Hotstart DNA polymerase was purchased from Thermofisher. Sanger sequencing was supplied by Eurofins. Routine manipulation of S. aureus and E. coli was performed as described by Monk et al. (3 (link)). X-Gal (5-bromo-4-chloro-3-indolyl-β-d -galactopyranoside; Melford) was used at 50 µg/ml in E. coli and 100 µg/ml in S. aureus. Antibiotics were purchased from Sigma Aldrich and used at the following concentrations: carbenicillin (Car), 100 µg/ml; chloramphenicol (Cm), 10 µg/ml; and kanamycin (Kan), 50 µg/ml (E. coli) and 100 µg/ml (S. aureus).
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Monks
Monks
Monks are members of a religious community who have taken vows of poverty, chastity, and obedience.
They typically live in a monastery or convent, following a common rule of life and engaging in activities such as prayer, study, and manual labor.
Monks have played a significant role in the history of Western civilization, contributing to the preservation and dissemination of knowledge, as well as the development of art, architecture, and various industries.
They have also been influential in the spiritual and cultural life of many societies.
Desptie their cloistered lifestyle, monks have often had a profound impact on the world around them.
They typically live in a monastery or convent, following a common rule of life and engaging in activities such as prayer, study, and manual labor.
Monks have played a significant role in the history of Western civilization, contributing to the preservation and dissemination of knowledge, as well as the development of art, architecture, and various industries.
They have also been influential in the spiritual and cultural life of many societies.
Desptie their cloistered lifestyle, monks have often had a profound impact on the world around them.
Most cited protocols related to «Monks»
5-bromo-4-chloro-3-indolyl beta-galactoside
Antibiotics
Bacteria
Buffers
Carbenicillin
Cell Wall
Chloramphenicol
DNA-Directed DNA Polymerase
DNA Restriction Enzymes
Escherichia coli
Galactose
Genome
Kanamycin
Lysostaphin
Monks
Oligonucleotides
Plasmids
Promega
Staphylococcus
Staphylococcus aureus
Strains
T4 DNA Ligase
Biological Assay
Cell Lines
Cell Survival
Claudins
Dreams
ERBB2 protein, human
Genome
Gold
Growth Disorders
Hypersensitivity
Malignant Neoplasm of Breast
MCF-7 Cells
Monks
Pharmaceutical Preparations
Phenobarbital
Technique, Dilution
Therapeutics
Chinese
Cultural Evolution
Emotions
Monks
Priests
Urban Population
Autopsy
Brain
Brain Death
Cognition
Cognitive Impairments, Mild
Dementia
Diagnosis
Disorders, Cognitive
Eligibility Determination
Ethics Committees, Research
Memory
Monks
Nuns
Personality Assessment
Physical Examination
Priests
Roman Catholics
The mindfulness intervention was delivered via the Headspace (www.headspace.com ) mindfulness-based smartphone app, and consisted of the app’s first 10 introductory sessions, named “Take 10.” These sessions are intended to act as a general introduction to mindfulness meditation and incorporate techniques such as breath awareness and body scanning. Each session has a duration of approximately 10 min and is guided by former Buddhist monk Andy Puddicombe. The app encourages users to complete one session a day, but this was not enforced. At the time of writing, Headspace has been downloaded more than 20 million times, is the highest scoring mindfulness-based iPhone app as per the Mobile Application Rating System (Mani et al. 2015 (link)), and has previously been shown to increase compassion (Lim et al. 2015 (link)) and well-being (Howells et al. 2014 (link)), and to reduce mind wandering (Bennike et al. 2017 ) and aggression (DeSteno et al. 2017 ).
A failure to utilize rigorous control or comparison conditions has previously been discussed as a major limitation in meditation research (Davidson and Kaszniak 2015 (link)). Here, a novel active control intervention was designed (in collaboration with the Brady Reynolds lab, University of Kentucky), which consisted of 10 excerpts from Andy Puddicombe’s audiobook The Headspace Guide to Meditation and Mindfulness. The sessions are narrated by Andy Puddicombe, are approximately 10 min in duration, and were delivered via the Headspace app, thus closely matching the mindfulness intervention across key attributes. Specifically, the user flow through the app was identical in both the mindfulness and audiobook conditions, differing only with regards to actual session content. The audiobook sessions, being predominantly psychoeducational, introduce the background and key concepts behind mindfulness, and include reflections from Andy Puddicombe’s experience training as a Buddhist monk. The chosen excerpts excluded any content which featured guided mindfulness exercises.
Participants were recruited via an email advertisement which was delivered via a third-party recruitment service (www.findparticipants.com ). The email linked participants to a screening and demographics questionnaire (see “Screening Questionnaire ”), hosted by SurveyMonkey (www.surveymonkey.com ). Within 24 h of completing the screening questionnaire, eligible participants were randomized, using simple randomization via a computer-generated sequence, to the experimental condition (mindfulness meditation via the Headspace app) or the active control condition (audiobook via the Headspace app), and emailed the baseline questionnaires. Alternative randomization procedures (such as blocked or stratified) were not used, as it is common in online studies for participants to withdraw after being randomized (but before beginning baseline assessments), which largely negates the benefits of such procedures. Participants were also provided with a Headspace voucher code, which restricted their access to either the experimental or control content, along with instructions on how to redeem their code and install the app. If a participant completed all 10 sessions of their intervention, they were automatically emailed the end-of-study questionnaires. Otherwise, they were considered to have withdrawn from the study. Participants were given up to 1 month to complete the intervention and did not receive any encouragement or reminder communications from the researchers. Those that completed the intervention were sent a final email thanking them for their participation, which included a £25 (or equivalent) Amazon voucher as compensation for their time. The entire experiment was run online.
A failure to utilize rigorous control or comparison conditions has previously been discussed as a major limitation in meditation research (Davidson and Kaszniak 2015 (link)). Here, a novel active control intervention was designed (in collaboration with the Brady Reynolds lab, University of Kentucky), which consisted of 10 excerpts from Andy Puddicombe’s audiobook The Headspace Guide to Meditation and Mindfulness. The sessions are narrated by Andy Puddicombe, are approximately 10 min in duration, and were delivered via the Headspace app, thus closely matching the mindfulness intervention across key attributes. Specifically, the user flow through the app was identical in both the mindfulness and audiobook conditions, differing only with regards to actual session content. The audiobook sessions, being predominantly psychoeducational, introduce the background and key concepts behind mindfulness, and include reflections from Andy Puddicombe’s experience training as a Buddhist monk. The chosen excerpts excluded any content which featured guided mindfulness exercises.
Participants were recruited via an email advertisement which was delivered via a third-party recruitment service (
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Awareness
Human Body
Meditation
Mindfulness
Monks
Muscle Rigidity
Reflex
Training Programs
Vaginal Diaphragm
Most recents protocols related to «Monks»
The null mutant lacking the putative serotonin N-acetyltransferase-encoding gene in S. pseudintermedius ED99 was constructed using the plasmid pBASE6 (Geiger et al., 2012 (link)). Briefly, pBASE6 was linearized using EcoRV and ~ 1,000 bp upstream and ~ 1,000 bp downstream fragments of the gene of interest were amplified from the genomic DNA of S. pseudintermedius ED99. The fragments were fused by Gibson Assembly (Gibson et al., 2009 (link)) using Hi-Fi DNA Assembly Master Mix (New England Biolabs). The resulting plasmid was first introduced into E. coli DC10B (Monk et al., 2012 (link)) and then into ED99. The deletion mutant construction was performed as previously described (Bae and Schneewind, 2006 (link)). Deletion of the genes were confirmed by PCR and sequence analysis. The mutants were named as described in the Supplementary Table S1 . Oligonucleotides used are listed in the Supplementary Table S2 .
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Deletion Mutation
Escherichia coli
Gene Deletion
Genes
Genome
Monks
NAT2 protein, human
Oligonucleotides
Plasmids
Sequence Analysis
The influence on cell growth of selected samples was evaluated following the protocol described by Monks et al. [12 (link)] with adaptations [13 (link)]. In 96-well plates, CHO-K1 cells (4 × 104 cell mL−1, 100 µL well−1) were exposed to each sample (0.25, 2.5, 25 and 250 µg mL−1, final concentrations) for 4 and 48 h. In the 4 h exposure experiment, after the first 4 h, the medium was removed, and CHO-K1 cells were kept in fresh complete medium for 20 h. A T0 plate representing the cell density at the time of sample treatment was made (T0untreated cells). At each experimental plate (4 + 20 h and 48 h), untreated cells were kept in the complete medium (T1untreated cells). The cell viability was evaluated by total protein quantification at 540 nm with the sulforhodamine assay. For each sample, the influence of each concentration on cell growth was expressed in percentage, considering (T1untreated cells–T0untreated cells) as 100% cell growth. The sample concentration required by eliciting 50% cell growth inhibition (GI50) was calculated by sigmoidal regression.
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Acclimatization
Biological Assay
Cells
Cell Survival
CHO Cells
Monks
Proteins
Psychological Inhibition
Specimen Handling
‘Friar’ (Prunus salicina Lindl.) plum fruit were harvested at commercial maturity (average single fruit weight: 117.00 ± 8.43 g; soluble solids content: 11.01 ± 0.13% and firmness: 70.36 ± 6.90 N) from an orchard located in Yixian county, Hebei Province, China (39°02′–39°35′ N, 114°51′–115°37′ E), and then immediately transported to the laboratory within 2 h on August 11, 2018. The fruit with uniform weight and shape, without visible defects were selected as materials, and the treatments were carried out as follows:
For different temperatures storage: The fruit were randomly divided into three groups (each about 350 fruit), and then were directly stored at 25 ± 1 °C (25 °C), 10 ± 0.5 °C (10 °C), and 0 ± 0.5 °C (0 °C), respectively. The ethylene production rate and anthocyanin content were observed at 0, 7, 14, 21, and 28 days of storage, and then the flesh samples were quickly frozen in liquid nitrogen and stored at −80 °C until used. Three replicates were performed for each treatment with 10 fruit per replicate.
For ethylene (ETH) and 1-methylcyclopropene (1-MCP) treatments: The plum fruit were randomly divided into three groups (each about 350 fruit). The fruit were carefully put into a sealed plastic box, and then were exposed to 100.0 μL L−1 ethylene and 1.0 μL L−1 1-MCP at 25 ± 2 °C for 20 h, respectively. The group with air was set as control. After treatment, plum fruit were stored at 10 °C. The ethylene production rate and anthocyanin content were observed at initial (pre-treatment), 0, 7, 14, 21, and 28 days after treatment, and then the flesh samples were quickly frozen in liquid nitrogen and stored at −80 °C until used. Three replicates were performed for each treatment with 10 fruits per replicate.
For different temperatures storage: The fruit were randomly divided into three groups (each about 350 fruit), and then were directly stored at 25 ± 1 °C (25 °C), 10 ± 0.5 °C (10 °C), and 0 ± 0.5 °C (0 °C), respectively. The ethylene production rate and anthocyanin content were observed at 0, 7, 14, 21, and 28 days of storage, and then the flesh samples were quickly frozen in liquid nitrogen and stored at −80 °C until used. Three replicates were performed for each treatment with 10 fruit per replicate.
For ethylene (ETH) and 1-methylcyclopropene (1-MCP) treatments: The plum fruit were randomly divided into three groups (each about 350 fruit). The fruit were carefully put into a sealed plastic box, and then were exposed to 100.0 μL L−1 ethylene and 1.0 μL L−1 1-MCP at 25 ± 2 °C for 20 h, respectively. The group with air was set as control. After treatment, plum fruit were stored at 10 °C. The ethylene production rate and anthocyanin content were observed at initial (pre-treatment), 0, 7, 14, 21, and 28 days after treatment, and then the flesh samples were quickly frozen in liquid nitrogen and stored at −80 °C until used. Three replicates were performed for each treatment with 10 fruits per replicate.
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1-methylcyclopropene
Aftercare
Anthocyanins
CCL2 protein, human
CCL8 protein, human
DNA Replication
Ethylenes
Freezing
Fruit
Monks
Nitrogen
Plum
Prunus salicina
Cells were harvested from 2 L YPD cultures, crude membranes prepared, and CauErg11-6×His, CauErg11 Y132F-6×His, CauErg11 K143R-6×His, or CauMdr1-6×His partially purified by nickel–nitrilotriacetic acid (Ni-NTA) affinity chromatography, essentially as described by Monk et al. [35 (link)]. The crude membranes were extracted in pH 7.5 solubilization buffer (10% (w/v) glycerol, 250 mM NaCl, 20 mM Tris, 0.5 mM PMSF, 1 tablet cOmpleteTM Mini, EDTA-free Protease Inhibitor cocktail (Roche, Basel, Switzerland) per 50 mL plus 16 mM n-decyl-β-D-maltopyranoside (DM Anagrade, Anatrace Products, LLC., Maumee, OH, USA). The detergent-solubilized protein affinity purified by binding to 2 mL of Ni-NTA Agarose matrix (Qiagen, Hilden, Germany) per g of protein in a disposable Econo-Pac® Chromatography column (Bio-Rad) was washed with 2 mM L-histidine and eluted with 100 mM L-histidine. The eluted protein was concentrated to 500 µL using Amicon® Ultra–4 Centrifugal Filter Units with a 50 kDa cutoff (Merck Millipore Ltd., Tullagreen, Ireland). Samples (1 µL) were separated by SDS-PAGE to obtain Coomassie-blue-stained protein bands for mass spectrometry of tryptic fragments. Tryptic fragments from the SDS-PAGE separated CauCdr1-6×His-containing band in crude membranes were used for mass spectrometry. For protein identification, the obtained fragments were searched against the Swiss-Prot database, the sequence of interest, and S. cerevisiae database to exclude possible background contamination.
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Buffers
Cells
Chromatography
Chromatography, Affinity
Coomassie blue
Detergents
Edetic Acid
G-substrate
Glycerin
GTP-Binding Proteins
Mass Spectrometry
Monks
nickel nitrilotriacetic acid
Protease Inhibitors
Proteins
Proto-Oncogene Mas
Saccharomyces cerevisiae
SDS-PAGE
Sepharose
Sodium Chloride
Spectrometry
Strains
Tablet
Tissue, Membrane
Tromethamine
Trypsin
This study is focusing on the semi-domesticated cats residing in monasteries, in Bangkok metropolitan, the capital of Thailand. Stratified randomization was conducted by selecting 43 monasteries and 24 districts in three zones for the sampling areas. Population size was calculated according to the Taro Yamane method [24 ] and 500 samples were collected from this study. Two to three monasteries were randomly selected in each district, and five to ten cats were sampled in each monastery. Animal health was examined by a qualified veterinarians prior to sample collection. The form of consent was informed to the animal’s caretakers before sample and data collection. Fecal samples were collected from the rectum, it was immediately placed in a dry bag and stored at 4 °C before transportation to the Department of parasitology, Faculty of Veterinary Medicine Kasetsart University, Bangkok before DNA extraction. A questionnaire was designed to collect animal information on age, sex, free-roaming, veterinary attention, previously deworming and Bangkok zone by interviewing the monks or animal caretakers during sample collection.
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Animals
Attention
Faculty
Feces
Felis catus
Monks
Rectum
Specimen Collection
Taro
Veterinarian
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More about "Monks"
Religious Ascetics, Monastics, Cloistered Individuals, Cenobites, Religious Recluses, Mendicants, Contemplative Practitioners, Coenobites, Claustral Residents, Monastic Orders, Monastic Brethren, Monastic Devotees, Monastic Dwellers, Monastic Inhabitants, Monastic Members, Monastic Occupants, Monastic Residents, Monastic Sojourners, Monastic Tenants.
Monks have played a pivotal role in the preservation and dissemination of knowledge throughout history, contributing to the development of art, architecture, and various industries.
Their cloistered lifestyle has often had a profound impact on the world around them.
Researchers and scientists can leverage the power of AI-driven comparisons using tools like PubCompare.ai to identify the best research protocols and products, streamlining their workflow and enhancing the accuracy and reproducibility of their studies.
By accessing a vast library of research protocols from literature, pre-prints, and patents, scientists can navigate the complex world of academic research with ease, unleashing their full scientific potential.
Cutting-edge imaging systems like the Odyssey CLx, combined with powerful software like FL Winlab v4.00.03, offer researchers the ability to analyze samples with precision and clarity.
Fluorescent dyes like IRDye 680RD and IRDye 800CW, as well as tools like the E.Z.N.A.® Blood DNA Mini Kit and Monochromators, provide researchers with the necessary tools to conduct their experiments effectively.
The LS 55 luminescence spectrometer and Prism version 5 statistical analysis software further enhance the researchers' ability to interpret their findings, ensuring accurate and reliable results.
Whether you're studying the historical impact of monasticism or leveraging the latest scientific advancements, the insights and resources available can help you achieve your research goals with greater efficiency and confidence.
Monks have played a pivotal role in the preservation and dissemination of knowledge throughout history, contributing to the development of art, architecture, and various industries.
Their cloistered lifestyle has often had a profound impact on the world around them.
Researchers and scientists can leverage the power of AI-driven comparisons using tools like PubCompare.ai to identify the best research protocols and products, streamlining their workflow and enhancing the accuracy and reproducibility of their studies.
By accessing a vast library of research protocols from literature, pre-prints, and patents, scientists can navigate the complex world of academic research with ease, unleashing their full scientific potential.
Cutting-edge imaging systems like the Odyssey CLx, combined with powerful software like FL Winlab v4.00.03, offer researchers the ability to analyze samples with precision and clarity.
Fluorescent dyes like IRDye 680RD and IRDye 800CW, as well as tools like the E.Z.N.A.® Blood DNA Mini Kit and Monochromators, provide researchers with the necessary tools to conduct their experiments effectively.
The LS 55 luminescence spectrometer and Prism version 5 statistical analysis software further enhance the researchers' ability to interpret their findings, ensuring accurate and reliable results.
Whether you're studying the historical impact of monasticism or leveraging the latest scientific advancements, the insights and resources available can help you achieve your research goals with greater efficiency and confidence.