(A) Schematic of experimental timeline; details are as follows.

Slides:



Advertisements
Similar presentations
THREE SIMPLE STEPS FOR PROCESSING SEMEN VIA SPERMPREP™II FILTER (SP-II) SpermPrep™II IT IS AS SIMPLE AS A-B-C! All specimens should be “washed” prior to.
Advertisements

ViahanceTM: Dead Cell, Stripped Nuclei and Free Oligonucleotide Removal Kit Instructions ViahanceTM dead cell removal kit enhances the viability ratio.
BioEnergy Production from Food Waste
Protein purification in practice Quantification of the procedure –How well did it work? –Did something go wrong? Where? Know how much fumarase is present.
IMMUNOLOGY LABORATORY PBMC ISOLATION SOP by Kizza D Martin Ssemambo
Extraction of “clay fraction”.
Experiment No 4. 5 Experiment Material and Chemicals Overview Introduction Procedure Objective
Extraction of Nucleic Acids (Genomic DNA, mRNA and Plasmid DNA)
Tian He Media non-selective: YPD without antibiotics Selective: Synthetic complete dropout medium (SC) (auxotroph) YPD with antibiotics.
ALGALTOXKIT F Test procedure. 1 PREPARATION OF ALGAL CULTURING MEDIUM - VOLUMETRIC FLASK (1 liter) - VIALS WITH NUTRIENT STOCK SOLUTIONS A (2 vials),
Increasing biogas production by thermal (70◦C) sludge pre- treatment prior to thermophilic anaerobic digestion Presented by Reem Satti.
Chelex ® Extraction. Learning Objectives Competence in extraction of different biological stains. Knowledge of the theory of DNA Isolation using Chelex.
Purification of DNA from a cell extract In addition to DNA, bacterial cell wall extract contain significant quantities of protein and RNA. A variety of.
Naagarajan Narayanan Vignesh Muthuvijayan* Department of Biotechnology
Autologous serum eye drops in severe post-LASIK dry eye.
Cat # SL Store at 4 0 C GenJet In Vitro DNA Transfection Reagent A Protocol for Transfections of Bacmids Into Sf9 Cells 100 l 500 l 1000.
Utility of Calcofluor M2R and Sytox Green Dual Staining for Assessment of Microsporidia Thelohania solenopsae Invading Solenopsis invicta M. Walker Hale.
Experiment 11 Isolation and purification of nuclei.
Isolation of Bacteriophages
S YNTHESIS AND CHARACTERIZATION OF C ROSS - LINKED CELLULASE ENZYME AGGREGATES (CLEA S ) BY ETHANOL AND ACETONE DESOLVATION TECHNIQUE Presentation by Jagdish.
min 30 min 45 min 60 min KDa Figure S1. SDS-PAGE of supernatant after incubation in digestion buffer. L. monocytogenes.
Preparation of Metaphase Chromosomes from culturing cells.
Protocol Electro-transformation : Select a snigle colony of E.coli from fresh LB plate and inoculate to 10 ml LB broth medium.Incubate until to reach.
Tubes centrifuged at room temperature for 10,000 rpm for 10 mins (to precipitate bacterial cells) (Control) E.coli (24h old culture) a loopful /tube was.
Introduction Materials and methods References For further information Name Mohammed T. Al-Othmani IBRAHIM H. IBRAHIM et al.
© 2013 Pearson Education, Inc. Bell Ringer  What is an endospore, and what special characteristics do endospore forming bacteria have?
Protein Purification bYSY.
Factors Affecting Solution Formation
Kinematic viscosity measurements
Virus Propagation in Embryonating Eggs
RNA fraction WASH 3X 0.3M guanidine hydrochloride in 95% EtOH
Drinking-water Treatment
Physical chemistry experiment
Extraction of “clay fraction”.
In Vitro Generation of Infectious Scrapie Prions
Volume 152, Issue 4, Pages (March 2017)
Mini-Prep Plasmid Isolation and Identification
Salt-extractability of H3K9me3, histone H3, and HP1α in mock cells and RPE cells expressing FLAG-SYCE2. Salt-extractability of H3K9me3, histone H3, and.
Taxonomic composition of subway microbial communities.
Representative radio-HPLC chromatograms for individual pooled methanolic fecal extracts for periods of maximum recovery of radioactivity after dosing of.
Protein Sample Preparation For NMR Screening
Biochemical Methodology
Fecal microbial transplantation
Gut microbial diversity of mice in voluntary and forced exercise groups. Gut microbial diversity of mice in voluntary and forced exercise groups. Weighted.
Practical Blood Bank Lab 1 ABO Grouping.
A small number of bacteria showed high levels of growth in the storage studies. A small number of bacteria showed high levels of growth in the storage.
Predicted microbiota age against the actual age of visitors and villagers. Predicted microbiota age against the actual age of visitors and villagers. (A)
Orthogonal partial least-squares discriminant analysis (OPLS-DA) plot for LC-MS/MS metabolite features. Orthogonal partial least-squares discriminant analysis.
Heatmaps of differential OTUs
Diagram of experimental design.
Investigation of the effect of ALE on fasting blood glucose level
Coral Bleaching Independent of Photosynthetic Activity
Effects of FMT in sows and/or offspring on brush border enzyme activity (A) and the expression of 11 selected genes in the duodenal mucosa (B) in offspring.
Effects of FMT in sows and/or offspring on median relative abundances (%) of bacterial phyla (A and B) and genera (C and D) in offspring fecal samples.
Presentation one: Synthesis of PHB
The Rab GTPase Ypt1p and Tethering Factors Couple Protein Sorting at the ER to Vesicle Targeting to the Golgi Apparatus  Pierre Morsomme, Howard Riezman 
Volume 8, Issue 7, Pages (July 2001)
Variations in genus-level Shannon diversity of offspring microbiota in fecal samples at 50 days of age (A) and ileal digesta at ~155 days of age (B) as.
Comparison of fecal metabolite concentrations in breast-fed (BF, green), standard formula-fed (FF, red), and B. lactis-supplemented formula-fed (FF + B.
Schematic representation of experimental design for BSp dietary treatments. Schematic representation of experimental design for BSp dietary treatments.
Effects of FMT in sows and/or offspring on intestinal histology in offspring, including villus height (A), villus width (B), crypt depth (C), villus height/crypt.
Microbial communities of the differently treated mice with lupus cluster separately after treatment. Microbial communities of the differently treated mice.
Functional assessment of B
Shifts in the microbial community compositions of the control and antibiotic groups. Shifts in the microbial community compositions of the control and.
Preparation of QC and Training Panels
Flowchart and study design schematic.
Effects of FMT on volatile fatty acid concentrations in the ileum (A), cecum (B), and colon (C) of offspring at ~155 days of age. Effects of FMT on volatile.
Detection of spiked bacteria.
Cvt19 Is a Receptor for the Cytoplasm-to-Vacuole Targeting Pathway
Iron concentration is higher in the serum of TPs than that of HVs
Presentation transcript:

(A) Schematic of experimental timeline; details are as follows. (A) Schematic of experimental timeline; details are as follows. Sow treatment groups comprised control (CON) (n = 9) and fecal microbiota transplantation procedure (FMTP) (n = 9) groups; the FMTP is described in Materials and Methods. “Pre-Ab” is preantibiotic, and “Post-Ab” is 4 days postantibiotic. On days 70 and 100, 200-ml fecal inocula were given to sows via gastric intubation. Post-first FMT fecal sampling was done 30 days after the first FMT, i.e., on day 100 of gestation. Post-second FMT fecal sampling was done 12 days after the second FMT, i.e., on day 112 of gestation. FMT1 treatment comprised a single 8-ml fecal inoculum given orally to offspring at birth, and FMT4 treatment comprised 8-ml fecal inocula given orally to offspring at birth and at 3, 7, and 28 days of age. (B) Schematic of fecal inoculum preparation; details are as follows. Pooled fecal samples were homogenized in maximum recovery diluent (MRD; Oxoid Ltd.) by stirring at 1,000 rpm for 10 min using a magnetic stirrer and then strained through a sieve to remove large particles, which were then washed through the sieve with another part of MRD. The homogenate was centrifuged for 30 min at 4,000 × g, and the supernatant discarded. Aliquots of the pellets in MRD + glycerol were stored at 5°C to allow microbial adjustment to low temperatures and then stored for no longer than 3 months at −80°C. (C) Schematic of study design and sample analysis. Ursula M. McCormack et al. mSystems 2018; doi:10.1128/mSystems.00134-17