Centrifugation
Centrifugation, Density Gradient
Centrifugation, Zonal
Centrifugation, Isopycnic
Cell Fractionation
Metrizamide
Microscopy, Electron
Subcellular Fractions
Povidone
Electrophoresis, Polyacrylamide Gel
Ultracentrifugation
Hypergravity
Filtration
Cell Membrane
Chromatography, Gel
Sucrose
Organoids
Cesium
Cattle
Liver
Solubility
Detergents
Chromatography
Silicon Dioxide
Nucleotidases
Hydrogen-Ion Concentration
Diatrizoate
Acid Phosphatase
Rabbits
Macromolecular Substances
Lysosomes
Microsomes
Spermatozoa
Membranes
Chemical Precipitation
Temperature
Chromatography, DEAE-Cellulose
Amino Acids
Colloids
Cells, Cultured
Electrophoresis
Carbon Isotopes
Cell-Free System
Rats, Inbred Strains
Octoxynol
Magnesium
Polyethylene Glycols
Escherichia coli
DNA
Phospholipids
Chromatography, Ion Exchange
Microbodies
Phosphotungstic Acid
Erythrocytes
Membrane Proteins
Proteins
Chromatography, Affinity
Cytoplasm
Organelles
Blood Specimen Collection
Intracellular Membranes
Cell Nucleus
Succinate Dehydrogenase
Phosphorus Isotopes
Carbohydrates
Adenosine Triphosphatases
Electrophoresis, Disc
Immunodiffusion
Evaluation Studies as Topic
Edetic Acid
Sperm Motility
Glucose-6-Phosphatase
RNA
Chemistry Techniques, Analytical
Molecular Sequence Data
Chemical Fractionation
Culture Media
Dialysis
Protein Binding
Ribosomes
Culture Techniques
Cytosol
Surface-Active Agents
Sodium Dodecyl Sulfate
Mitochondria, Liver
Chemistry
Erythrocyte Aging
Tissue Extracts
Chemical Phenomena
Immune Sera
Specimen Handling
Trypsin
Fluorescent Antibody Technique
Swine
Mitochondria
Spectrophotometry
Chromatography, High Pressure Liquid
Amino Acid Sequence
Semen
Adenosine Triphosphate
Polyribosomes
Nucleic Acid Hybridization
Digitonin
Reticulocytes
Electron Transport Complex IV
Glycoproteins
Peptide Hydrolases
Ultrafiltration
Urate Oxidase
Plants
Complement Fixation Tests
Mucins
Nucleic Acid Renaturation
Malate Dehydrogenase
Densitometry
Biological Transport
Carbon Radioisotopes
Blood
Spheroplasts
Nucleic Acid Denaturation
Microscopy, Phase-Contrast
Hexosaminidases
Peptides
Protein Biosynthesis
Alkaline Phosphatase
Osmolar Concentration
Electrophoresis, Agar Gel
Extrachromosomal Inheritance
Cricetinae
Gravitation
Staining and Labeling
Golgi Apparatus
Histocytochemistry
DNA, Circular
Coxiella
Kidney
Endoplasmic Reticulum
Substrate Specificity
Cryopreservation
Cytochromes
Binding Sites
Oxidoreductases
Semen Preservation
Lipids
Lymphocytes
Hydrolases
Calcium
Microsomes, Liver
Base Sequence
RNA, Messenger
Chloroform
Guinea Pigs
Haplorhini
Protamines
Semen Analysis
Buffers
Blood Platelets
Species Specificity
Adsorption
Autoradiography
Chick Embryo
Nuclear chromatin variations in human spermatozoa undergoing swim-up and cryopreservation evaluated by the flow cytometric sperm chromatin structure assay. (1/1626)
The sperm chromatin structure assay (SCSA) is a flow cytometric (FCM) technique which exploits the metachromatic properties of Acridine Orange to monitor the susceptibility of sperm chromatin DNA to in-situ acid denaturation. SCSA was used to study the chromatin structure variations of human spermatozoa in semen, both before and after swim-up and after cryopreservation. Semen samples were provided by 19 healthy normozoospermic subjects attending pre-marriage checks. Each sample was divided into three aliquots: the first aliquot was evaluated without further treatment, the second underwent swim-up, and the third was stored according to standard cryopreservation techniques in liquid nitrogen at -196 degrees C. Samples were also analysed by light and fluorescence microscopy (after Acridine Orange staining to evaluate the number of green fluorescent sperm heads), and by computer-assisted semen analysis. The results showed that post-rise spermatozoa represent a subpopulation characterized by a general improvement of the morphological (reduction of the percentage of abnormal forms and heads, increase of the green head sperm percentage) and kinetic parameters. This subpopulation also exhibited improved chromatin structure properties, confirming that these cells have the best structural and functional characteristics, indicative of optimal fertilizing ability. On the other hand, overall sperm quality deteriorates after cryopreservation. When thawed spermatozoa underwent an additional swim-up round, a general improvement of nuclear maturity was seen in the post-rise spermatozoa. (+info)Mechanically induced c-fos expression is mediated by cAMP in MC3T3-E1 osteoblasts. (2/1626)
In serum-deprived MC3T3-E1 osteoblasts, mechanical stimulation caused by mild (287 x g) centrifugation induced a 10-fold increase in mRNA levels of the proto-oncogene, c-fos. Induction of c-fos was abolished by the cAMP-dependent protein kinase inhibitor H-89, suggesting that the transient c-fos mRNA increase is mediated by cAMP. Down-regulation of protein kinase C (PKC) activity by chronic TPA treatment failed to significantly reduce c-fos induction, suggesting that TPA-sensitive isoforms of PKC are not responsible for c-fos up-regulation. In addition, 287 x g centrifugation increased intracellular prostaglandin E2 (PGE2) levels 2.8-fold (P<0. 005). Since we have previously shown that prostaglandin E2 (PGE2) can induce c-fos expression via a cAMP-mediated mechanism, we asked whether the increase in c-fos mRNA was due to centrifugation-induced PGE2 release. Pretreatment with the cyclooxygenase inhibitors indomethacin and flurbiprofen did not hinder the early induction of c-fos by mechanical stimulation. We conclude that c-fos expression induced by mild mechanical loading is dependent primarily on cAMP, not PKC, and initial induction of c-fos is not necessarily dependent on the action of newly synthesized PGE2. (+info)A novel strategy for the preparation of liposomes: rapid solvent exchange. (3/1626)
During the preparation of multi-component model membranes, a primary consideration is that compositional homogeneity should prevail throughout the suspension. Some conventional sample preparation methods pass the lipid mixture through an intermediary, solvent-free state. This is an ordered, solid state and may favor the demixing of membrane components. A new preparative method has been developed which is specifically designed to avoid this intermediary state. This novel strategy is called rapid solvent exchange (RSE) and entails the direct transfer of lipid mixtures between organic solvent and aqueous buffer. RSE liposomes require no more than a minute to prepare and manifest considerable entrapment volumes with a high fraction of external surface area. In phospholipid/cholesterol mixtures of high cholesterol content, suspensions prepared by more conventional methods reveal evidence of artifactual demixing, whereas samples prepared by rapid solvent exchange do not. The principles which may lead to artifactual demixing during conventional sample preparation are discussed. (+info)Chromosome-membrane association in Bacillus subtilis. IV. Further purification of DNA-membrane complex by using a combination of centrifugation and electrophoresis. (4/1626)
We have developed a simple procedure to purify a DNA-membrane complex from Bacillus subtilis by using a combination of centrifugation and electrophoresis. Several unique proteins were detected in the purified complex. (+info)Vasopressin regulates apical targeting of aquaporin-2 but not of UT1 urea transporter in renal collecting duct. (5/1626)
In the renal inner medullary collecting duct (IMCD), vasopressin regulates two key transporters, namely aquaporin-2 (AQP2) and the vasopressin-regulated urea transporter (VRUT). Both are present in intracellular vesicles as well as the apical plasma membrane. Short-term regulation of AQP2 has been demonstrated to occur by vasopressin-induced trafficking of AQP2-containing vesicles to the apical plasma membrane. Here, we have carried out studies to determine whether short-term regulation of VRUT occurs by a similar process. Cell surface labeling with NHS-LC-biotin in rat IMCD suspensions revealed that vasopressin causes a dose-dependent increase in the amount of AQP2 labeled at the cell surface, whereas VRUT labeled at the cell surface did not increase in response to vasopressin. Immunoperoxidase labeling of inner medullary thin sections from Brattleboro rats treated with 1-desamino-8-D-arginine vasopressin (DDAVP) for 20 min revealed dramatic translocation of AQP2 to the apical region of the cell, with no change in the cellular distribution of VRUT. In addition, differential centrifugation of inner medullary homogenates from Brattleboro rats treated with DDAVP for 60 min revealed a marked depletion of AQP2 from the low-density membrane fraction (enriched in intracellular vesicles) but did not alter the quantity of VRUT in this fraction. Finally, AQP2-containing vesicles immunoisolated from a low-density membrane fraction from renal inner medulla did not contain immunoreactive VRUT. Thus vasopressin-mediated regulation of AQP2, but not of VRUT, depends on regulated vesicular trafficking to the plasma membrane. (+info)Evidence that the co-chaperone p23 regulates ligand responsiveness of the dioxin (Aryl hydrocarbon) receptor. (6/1626)
The dioxin (aryl hydrocarbon) receptor is a ligand-dependent transcription factor that induces expression of a number of genes encoding drug metabolizing enzymes. In the absence of ligand the dioxin receptor is present in the cytoplasmic compartment of the cell associated with the molecular chaperone hsp90, which has been implicated in regulating the correct folding of the ligand binding domain of the receptor. In this study we have examined a potential role of the hsp90-associated p23 protein in the activation process of the dioxin receptor to a DNA binding form. In an in vitro model we show that addition of ligand alone to the dioxin receptor fails to induce release of hsp90 from the dioxin receptor. In the presence of ligand, this release was, however, induced upon addition of purified preparations of Arnt. Interestingly, p23 was also found to be associated with the nonactivated form of the dioxin receptor. Following fractionation on sucrose gradients p23 was dissociated from the receptor-hsp90 complex generating a receptor form, which showed ligand-independent release of hsp90 by Arnt and, consequently, ligand-independent activation of the DNA binding activity of the dioxin receptor. Ligand dependence was reconstituted in the presence of molybdate, a transition metal ion known to stabilize the interaction between the molecular chaperone hsp90 and p23. Taken together these experiments suggest a role of p23 in modulating ligand responsiveness in the activation process of the dioxin receptor. (+info)Visualizing ion relaxation in the transport of short DNA fragments. (7/1626)
Ion relaxation plays an important role in a wide range of phenomena involving the transport of charged biomolecules. Ion relaxation is responsible for reducing sedimentation and diffusion constants, reducing electrophoretic mobilities, increasing intrinsic viscosities, and, for biomolecules that lack a permanent electric dipole moment, provides a mechanism for orienting them in an external electric field. Recently, a numerical boundary element method was developed to solve the coupled Navier-Stokes, Poisson, and ion transport equations for a polyion modeled as a rigid body of arbitrary size, shape, and charge distribution. This method has subsequently been used to compute the electrophoretic mobilities and intrinsic viscosities of a number of model proteins and DNA fragments. The primary purpose of the present work is to examine the effect of ion relaxation on the ion density and fluid velocity fields around short DNA fragments (20 and 40 bp). Contour density as well as vector field diagrams of the various scalar and vector fields are presented and discussed at monovalent salt concentrations of 0.03 and 0.11 M. In addition, the net charge current fluxes in the vicinity of the DNA fragments at low and high salt concentrations are briefly examined and discussed. (+info)Characterization of Fus3 localization: active Fus3 localizes in complexes of varying size and specific activity. (8/1626)
The MAP kinase Fus3 regulates many different signal transduction outputs that govern the ability of Saccharomyces cerevisiae haploid cells to mate. Here we characterize Fus3 localization and association with other proteins. By indirect immunofluorescence, Fus3 localizes in punctate spots throughout the cytoplasm and nucleus, with slightly enhanced nuclear localization after pheromone stimulation. This broad distribution is consistent with the critical role Fus3 plays in mating and contrasts that of Kss1, which concentrates in the nucleus and is not required for mating. The majority of Fus3 is soluble and not bound to any one protein; however, a fraction is stably bound to two proteins of approximately 60 and approximately 70 kDa. Based on fractionation and gradient density centrifugation properties, Fus3 exists in a number of complexes, with its activity critically dependent upon association with other proteins. In the presence of alpha factor, nearly all of the active Fus3 localizes in complexes of varying size and specific activity, whereas monomeric Fus3 has little activity. Fus3 has highest specific activity within a 350- to 500-kDa complex previously shown to contain Ste5, Ste11, and Ste7. Ste5 is required for Fus3 to exist in this complex. Upon alpha factor withdrawal, a pool of Fus3 retains activity for more than one cell cycle. Collectively, these results support Ste5's role as a tether and suggest that association of Fus3 in complexes in the presence of pheromone may prevent inactivation in addition to enhancing activation. (+info)The signs and symptoms of CE can vary depending on the location of the tumor, but they may include:
* Lumps or swelling in the neck, underarm, or groin area
* Fever
* Fatigue
* Weight loss
* Night sweats
* Swollen lymph nodes
* Pain in the affected area
CE is caused by a genetic mutation that leads to uncontrolled cell growth and division. The exact cause of the mutation is not fully understood, but it is believed to be linked to exposure to certain viruses or chemicals.
Diagnosis of CE typically involves a combination of physical examination, imaging tests such as CT scans or PET scans, and biopsy to confirm the presence of cancer cells. Treatment options for CE depend on the stage and location of the tumor, but may include:
* Chemotherapy to kill cancer cells
* Radiation therapy to shrink the tumor
* Surgery to remove the tumor
* Immunotherapy to boost the immune system's ability to fight the cancer
Overall, CE is a rare and aggressive form of cancer that requires prompt diagnosis and treatment to improve outcomes.
Centrifugation
Differential centrifugation
Rate-zonal centrifugation
Buoyant density centrifugation
Peeler centrifuge
Ultracentrifuge
Partial specific volume
Laboratory centrifuge
Centrifuge
Gas centrifuge
Solid bowl centrifuge
Decantation
RNA polymerase
African trypanosomiasis
Trichuris
Soil salinity control
Blood culture
Ammonium sulfate
Post-excavation analysis
Elutriation
Plasmapheresis
Characterization of nanoparticles
Precipitation (chemistry)
Corn wet-milling
Clinical chemistry
Washed red blood cells
Temperature-responsive polymer
Sperm sorting
Diagnostic microbiology
Bioprocess
Separation of bacteria, protozoa and carbon nanotubes by density gradient centrifugation | NIST
Browsing by Subject "Centrifugation"
Fecal Centrifugation Testing - Vetstreet | Vetstreet
Lost in Centrifugation: Accounting for Transporter Protein Losses in Quantitative Targeted Absolute Proteomics | Drug...
Centrifugation, Density Gradient | Profiles RNS
Open Access Centrifugation Journals · OA.mg
Centrifugation Tube rack 81 wells Double Function | Pac Bio Supply
Microfuge 16, Benchtop Centrifuge
Profiling post-centrifugation delay of serum and plasma with antibody bead arrays.
A Modified Differential Centrifugation Protocol for Isolation and Quantitation of Extracellular Heat Shock Protein 90 (eHsp90)....
mAb Solutions for Biopharma Research - Eppendorf Hong Kong
Good Laboratory Practices for Waived Testing Sites
Survey Findings from Testing Sites Holding a Certificate of Waiver Under ...
Maximizing Precision and Efficiency in Antibody Cell Separation -- Uberstrainer | PRLog
EN (en)
ArboCat Virus: Matruh (MTRV)
How to Minimize Contamination Risk and Protect your Cell Cultures | Corning
ROS-induced R loops trigger a transcription-coupled but BRCA1/2-independent homologous recombination pathway through CSB |...
Protocol for Metagenomic Virus Detection in Clinical Specimens - Volume 21, Number 1-January 2015 - Emerging Infectious...
Glycolytic activity in human red cell populations separated by a combination of density and counterflow centrifugation....
HiSpeed Plasmid Mega and Giga EF Kits
Neuronal Pentraxins Mediate Synaptic Refinement in the Developing Visual System | Journal of Neuroscience
NIOSHTIC-2 Search Results - Full View
NIOSHTIC-2 Search Results - Full View
DRI-CHEM NX600V | Fujifilm [Italy]
NHANES 2011-2012:
Albumin & Creatinine - Urine Data Documentation, Codebook, and Frequencies
Cherry Chen Chen - Google Scholar
Procter & Gamble - Tampax® Pearl Super Plus Absorbency - Box of 18 | EarthTurns®
IJMS | Free Full-Text | An Isolated Complex V Inefficiency and Dysregulated Mitochondrial Function in Immortalized Lymphocytes...
Adipose extracellular matrix promotes skin wound healing by inducing the differentiation of adipose‑derived stem cells into...
Density gradient9
- Centrifugation, Density Gradient" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (sdsu.edu)
- This graph shows the total number of publications written about "Centrifugation, Density Gradient" by people in this website by year, and whether "Centrifugation, Density Gradient" was a major or minor topic of these publications. (sdsu.edu)
- Below are the most recent publications written about "Centrifugation, Density Gradient" by people in Profiles. (sdsu.edu)
- This process can be enhanced by using density gradient centrifugation to isolate specific cell types. (prlog.org)
- Here we describe a simple density gradient centrifugation method, which allows the rapid purification of infective metacyclic parasites from both wild-type and LPG-deficient Leishmania major. (pasteur.fr)
- It is argued that the combination of density gradient and counter-flow centrifugation offers a greater potential for obtaining an old red cell population than classical red cell density centrifugation alone. (vumc.nl)
- In October and December, fresh ejaculate was fractionated by centrifugation through a discontinuous density gradient of polyvinylpyrrolidone-coated silica particles (Percoll((R))**) to separate motile spermatozoa from other cells and seminal plasma. (cdc.gov)
- The physician who performed the inseminations reported that in January 1990 a second HIV-1-discordant couple (i.e., seropositive husband with hemophilia, sero negative wife) underwent one insemination using the same density gradient centrifugation procedure. (cdc.gov)
- Leukocytes remained in all four samples after simple centrifugation and washing and in two of three samples tested after density gradient centrifugation. (cdc.gov)
Differential3
- A Modified Differential Centrifugation Protocol for Isolation and Quantitation of Extracellular Heat Shock Protein 90 (eHsp90). (bvsalud.org)
- Among the half a dozen reported methodologies, differential centrifugation is considered the " gold standard" largely for its quantitative recovery of eHsp90α from a conditioned medium of cultured cells . (bvsalud.org)
- Microsomes were isolated by differential centrifugation of lung homogenate. (cdc.gov)
Serum1
- Profiling post-centrifugation delay of serum and plasma with antibody bead arrays. (scilifelab.se)
Elute1
- HiSpeed Plasmid Mega and Giga EF Kits provide vacuum-driven, large-scale, anion-exchange-based plasmid DNA preparation and require only one centrifugation step to elute the final plasmid DNA. (qiagen.com)
Supernatant2
- This unique module also eliminates the risk of pellet loss, which can occur during decanting of the supernatant following centrifugation. (qiagen.com)
- After centrifugation, the supernatant will be separated. (who.int)
Fecal12
- We demonstrate separation of protozoa (Tetrahymena thermophila) from MWCNTs, bacterial agglomerates, and protozoan fecal pellets by centrifugation in iodixanol solution. (nist.gov)
- Fecal centrifugation testing can identify intestinal parasites, which is important for determining the best treatment and helping to ensure a full recovery. (vetstreet.com)
- What Is Fecal Centrifugation? (vetstreet.com)
- Fecal diagnostic testing, such as fecal centrifugation, is an important part of this process. (vetstreet.com)
- Why Does My Pet Need a Fecal Centrifugation Test? (vetstreet.com)
- If your pet is showing any suspicious signs, your veterinarian may recommend fecal centrifugation testing to determine if parasites are the cause. (vetstreet.com)
- Parasites, viruses, and other medical problems aren't always apparent, so your veterinarian may recommend fecal centrifugation testing, along with some other diagnostic tests to help ensure that your new pet is healthy before being introduced to your other pets and family members. (vetstreet.com)
- How Is Fecal Centrifugation Performed? (vetstreet.com)
- To perform fecal centrifugation, your veterinarian places a small amount of fecal material into a test tube and mixes it with a special fecal flotation solution. (vetstreet.com)
- Studies have shown that fecal centrifugation permits the detection of more parasite eggs than some other forms of fecal analysis. (vetstreet.com)
- Some veterinarians perform fecal centrifugation testing in the office, so results may be available the same day. (vetstreet.com)
- Other practices send fecal material to an outside laboratory for centrifugation testing, so results may take a few days. (vetstreet.com)
Suitable2
- TwinSpin centrifugation tubes are suitable for efficiently separating peripheral blood mononuclear cells from whole blood and bone marrow. (prlog.org)
- The purified DNA is equivalent to that obtained by 2 x CsCl gradient centrifugation and is suitable for transfection-grade applications. (qiagen.com)
Tubes1
- Single binder and sandwich assays revealed decreasing levels of caldesmon 1 (CALD1) related to EDTA standard tubes and prolonged post-centrifugation delay of 36h. (scilifelab.se)
Protein2
- Multiplexed protein profiles of post-centrifugation delay were generated in 384 biotinylated samples using 373 antibodies that targeted 343 unique proteins. (scilifelab.se)
- By profiling three types of blood preparations for alterations in protein profiles with respect to time and temperature post centrifugation, we addressed an important component in the analysis and of such specimen. (scilifelab.se)
Separation2
- Cell separation by centrifugation is a method that separates cells based on their density. (prlog.org)
- Its exceptional separation properties result in DNA purity equivalent or superior to that obtained by two successive rounds of CsCl gradient centrifugation. (qiagen.com)
Antibody1
- The unattached fluorescent antibody is then removed by washing during centrifugation. (cdc.gov)
Procedure2
- The vacuum driven QIAfilter module replaces the centrifugation step in the classic anion-exchange procedure, making purification faster and more convenient. (qiagen.com)
- The unique QIAconcentrator (see figure " HiSpeed Plasmid Giga EF procedure "> HighSpeed Plasmid Giga EF procedure ") replaces the centrifugation step traditionally used to collect isopropanol-precipitated DNA following purification. (qiagen.com)
Bacterial2
- QIAfilter Cartridges (see figure " QIAfilter Mega-Giga Cartridge For fast purification of up to 10 mg transfection-grade plasmid or cosmid DNA "> QIAfilter Mega-Giga Cartridge ") are special filter units designed to replace the centrifugation step following alkaline lysis of bacterial cells. (qiagen.com)
- QIAfilter Cartridges completely remove SDS precipitates and clear bacterial lysates in a fraction of the time needed for centrifugation. (qiagen.com)
Time1
- [ 50 ] Optimal centrifugation time and speed are critical for concentrating Cryptosporidium oocysts. (medscape.com)
Cell2
- Glycolytic activity in human red cell populations separated by a combination of density and counterflow centrifugation. (vumc.nl)
- Red cells comprising the lowest and highest density fractions, respectively, were subsequently separated according to mean cell volume (MCV) by means of counterflow centrifugation. (vumc.nl)
Step1
- Step 2: Remove unbound proteins by centrifugation. (cellsignal.com)
Simple1
- In two, CD4+ lymphocytes were present after simple centrifugation and washing. (cdc.gov)
Samples1
- In case of whole blood samples, it will take another 2 minutes for the centrifugation for each sample. (fujifilm.com)
Team1
- Our team made this list of Centrifugation Open Access journals with the aim to help you to decide where to publish your Centrifugation manuscript. (oa.mg)
Website1
- en]We use cookies on our website to give you the most relevant experience by remembering your preferences and repeat visits. (pasteur.fr)
Method1
- Two-step centrifugation method. (nih.gov)
Test1
- This photograph shows Brent Bobick, Ph.D., Postdoctoral Fellow, examining a test tube for gradient centrifugation, a process that enriches adult human bone marrow-derived mesenchymal stem cells by removing smaller, unwanted cells, such as red blood cells. (nih.gov)
Times3
- We also assessed the effects of different centrifugation times on the TAT of results. (medscape.com)
- A few studies [ 8-10 ] have noted equivalent analytical accuracy for chemistry assays when using shorter centrifugation times when specimens are processed manually. (medscape.com)
- In this study, we report the effect of varying centrifugation times on the accuracy and precision of chemistry assays, TAT, and specimen stability using an automated specimen processing system for chemistry testing. (medscape.com)
Results2
- Reduced centrifugation time resulted in significant improvements in TAT, with a median TAT for STAT results decreasing from 38 minutes to 28 minutes. (medscape.com)
- Furthermore, marked reductions in the TAT of chemistry results are achieved by using a shorter centrifugation time. (medscape.com)