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Charcoal

Charcoal, a dark porous residue obtained by the heating of wood, peat, coconut shells, or other substances in the absence of air, has a variety of uses.
It can be used as a fuel, in purification processes, and in the production of various chemicals.
Charcoal is also used for medicinal purposes, such as in the treatment of poisoning and digestive disorders.
Researchers continue to explore the potential applications of charcoal, leveraging advanced technologies and methodologies to optimize its properties and unlock new possibilities.
Discover the latest advancements in charcoal research and development with PubCompare.ai, an AI-driven platform designed to enhance reproducibility and accuracy in your scientific inquiries.

Most cited protocols related to «Charcoal»

Newly sequenced mitogenomes from 42 diverse fish species were used in evaluating the performance of the MitoAnnotator pipeline. The 42 species are as follows (the International Nucleotide Sequence Database Collaboration accession numbers are provided): Acanthocybium solandri (AP012945), Anchoviella sp. (AP012524), Aphanopus carbo (AP012944), Ariomma indica (AP012513), Ariomma lurida (AP012512), Assurger anzac (AP012508), Benthodesmus tenuis (AP012522), Dionda episcopa (AP012077), Diplospinus multistriatus (AP012523), Epinnula magistralis (AP012943), Eumegistus illustris (AP012497), Euthynnus affinis (AP012946), Evoxymetopon poeyi (AP012509), Gempylus serpens (AP012502), Gymnosarda unicolor (AP012510), Hemitremia flammea (AP012078), Icichthys lockingtoni (AP012511), Kali indica (AP012500), Luciocyprinus striolatus (AP012525), Luxilus chrysocephalus (AP012079), Macrhybopsis gelida (AP012080), Margariscus margarita (AP012081), Microphysogobio yaluensis (AP012073), Nesiarchus nasutus (AP012503), Nocomis biguttatus (AP012082), Notropis atherinoides (AP012083), Notropis baileyi (AP012084), Opsopoeodus emiliae (AP012085), Pampus punctatissimus (AP012516), Peprilus burti (AP012947), Promethichthys prometheus (AP012504), Pteraclis aesticola (AP012499), Rastrelliger kanagurta (AP012948), Ruvettus pretiosus (AP012506), Sarda orientalis (AP012949), Scombrolabrax heterolepis (AP012517), Sphyraena japonica (AP012501), Tanakia tanago (AP012526), Taractes asper (AP012498), Tetragonurus atlanticus (AP012515), Tetragonurus cuvieri (AP012514), and Thyrsitoides marleyi (AP012505). The extracted mitogenomes were amplified via the long PCR technique (Miya and Nishida 1999 ; Inoue et al. 2003a (link)) and sequenced with the Sanger sequencing technique.
Publication 2013
affinis Base Sequence Charcoal Fishes Nucleotides

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Publication 2012
Age Groups Airborne Particulate Matter Air Pollution Animals Blood Pressure Carcinogens Charcoal Coal Coronary Arteriosclerosis Crop, Avian Feces Gender Glucose Health Risk Assessment High Blood Pressures Households Hypercholesterolemia Index, Body Mass physiology Plasma Population at Risk
To evaluate gastrointestinal transit parameters, an adaption of our established scintigraphic method was used [14 (link), 15 (link), 28 (link)]. Briefly, 0.1mCi 111InCl3 was mixed with a slurry of 5 mg of activated charcoal. The mixture was allowed to evaporate to dryness, after which the radiolabeled charcoal was packed into a gelatin capsule. This capsule was coated with one layer of methacrylate (Eudragit L, The Dow Chemical Company) which dissolves in a pH-sensitive manner upon reaching the alkaline terminal ileum, thus allowing radiolabel to be transferred to the colon for quantitation of colon transit. The 111In containing capsule was administered following an overnight fast. After this capsule had emptied from the stomach, subjects ingested a 99mTc-labeled meal. Estimation of colonic filling with 99mTc at 6 hours (CF6h) served as a surrogate for small bowel transit. Subjects ingested standardized meals for lunch and dinner, 4 and 8 hours after the radiolabeled breakfast, respectively. Using a gamma camera, abdominal images with anterior and posterior cameras of 2 minutes duration were acquired immediately following ingestion of the radiolabeled meal and at specified time points during the subsequent 48 hours period.
Publication 2009
Abdomen Acclimatization Capsule Charcoal Charcoal, Activated Colon Eudragit L Gamma Cameras Gelatins Ileum Intestines, Small Methacrylate Radionuclide Imaging Transits, Gastrointestinal
We used two methods for three-dimensional culture of prostate organoids from isolated prostate epithelial cells, corresponding to flotation on top of Matrigel or embedding within Matrigel; the embedding method was used for drug treatment experiments and is described below. For the floating method, prostate epithelial cells were resuspended in prostate organoid culture medium, consisting of: hepatocyte medium supplemented with 10 ng/ml epidermal growth factor (EGF) (Corning #355056), 10 μM Y-27632 (STEMCELL Technologies #07171), 1x glutamax (Gibco #35050), 5% Matrigel (Corning #354234), and 5% charcoal-stripped FBS (Gibco #12676), which had been heat-inactivated at 55°C for 1 hr. After resuspension in prostate organoid medium, 100 – 10,000 dissociated cells were plated into wells of ultra low-attachment 96 well plates (Corning #3474) in the presence of 100 nM DHT for mouse or 10 nM DHT for human (Sigma A-8380). 100 μl of fresh organoid medium was added to the wells every four days, and the medium changed every 12 days for up to one month.
For serial passaging experiments, organoids were passaged at a 1:4 dilution every 1–2 weeks with 0.25% trypsin for 5 minutes at 37°C, followed by mechanical dissociation to nearly single-cell suspensions. Organoids were frozen in complete media with 50% FBS and 10% DMSO. The efficiency of organoid formation was calculated by averaging the number of organoids visible in each well after 7 days of growth using a 10x objective. For statistical analyses, efficiency percentages were arcsin converted to perform unpaired two-tailed Student’s t-tests.
For analyses of androgen withdrawal, organoids were passaged and then cultured for 7–10 days in culture medium in the presence or absence of DHT. For induction of Cre recombinase activity in culture, epithelial cells from un-induced CK8-CreERT2; Ptenflox/flox; KrasLSL-G12D/+; R26R-CAG-YFP mice were sorted based on EpCAM and E-cadherin expression, and cultured until organoid formation was evident. The resulting organoids were passaged, followed by addition of 1 μM 4-OHT on the day after passaging to induce Cre recombination.
A detailed protocol for organoid establishment and culture will be provided on Nature Protocol Exchange immediately following publication.
Publication 2014
Androgens Cells Charcoal Cre recombinase Culture Media Culture Techniques dihydrotestosterone-17-N-bis(2-chloroethyl)carbamate E-Cadherin Epidermal growth factor Epithelial Cells Freezing Hepatocyte Homo sapiens matrigel Mus Organoids Pharmaceutical Preparations Prostate PRSS1 protein, human PRSS2 protein, human Recombination, Genetic Stem Cells Student Sulfoxide, Dimethyl TACSTD1 protein, human Technique, Dilution Therapies, Investigational Y 27632
LNCaP, CWR22Rv1, and VCaP human prostate cancer cell lines were obtained from the American Type Culture Collection (ATCC, Rockville, MD). Early passage cells were used in all experiments. LNCaP95 is an androgen-independent cell line derived from the parental LNCaP cells (provided by Dr. Alan K. Meeker, Johns Hopkins University, Baltimore, MD). LNCaP95 cells and the parental LNCaP cells demonstrate qualitatively similar AR transcriptional responses (Supplemental Figure 1). Previous studies have evaluated and estabished the expression status for both AR-FL and AR-V in these 4 cell lines (9 (link)). Stable clones of AR-FL positive and AR-FL negative LNCaP cells were developed by EB (Supplemental Methods). In all comparisons involving the treatment of cells with or without R1881 (NEN, Boston, MA), cells were cultured for indicated time periods in culture media without phenol red (Invitrogen, Carlsbad, CA) supplemented with 10% charcoal-stripped FBS (CSS) (Invitrogen) with or without 1 nM R1881 (NEN, Boston, MA). For siRNA treatment, cells reaching ~70% confluence were treated with siRNA for 24 hours and then cultured for 48 hours with or without 1 nM R1881. Target sequences for specific knockdown of different AR molecules were described previously (9 (link)). MDV3100 was obtained from Medivation (San Francisco, CA). VCaP and LNCaP 95 cells were treated with MDV3100 dissolved in DMSO at the indicated concentrations for 24 hours with or without 1 nM R1881 (NEN). Transient transfection with AR-Vs was performed as described previously (7 (link)–9 (link)).
Publication 2012
Androgens Cell Lines Cells Charcoal CHOP regimen Clone Cells Culture Media Homo sapiens MDV 3100 Parent Prostate Cancer R-1881 RNA, Small Interfering Sulfoxide, Dimethyl Transcription, Genetic Transfection Transients

Most recents protocols related to «Charcoal»

Example 4

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The title compound was prepared following general procedure B with Intermediate 1 (1.0 g, 1.0 equiv) and 2-amino-2-methylpropionitrile (436 mg, 1.1 eq). The crude product was purified by flash chromatography (50-100% ethyl acetate in heptanes) and treated with charcoal. The resulting residue was recrystallized from ethyl acetate (8 mL) to yield N-(2-cyanopropan-2-yl)-2-(5-((3-ethoxypyridin-2-yl)oxy)pyridin-3-yl)pyrimidine-5-carboxamide (1.1 g, 92%) as a colorless solid. 1H NMR (400 MHz, DMSO-d6) δ 1.38 (t, 3H), 1.74 (s, 6H), 4.18 (q, 2H), 7.18 (dd, 1H), 7.57 (dd, 1H), 7.69 (dd, 1H), 8.38 (dd, 1H), 8.66 (d, 1H), 9.18 (br. s, 1H), 9.30 (s, 2H), 9.40 (d, 1H). MS (ES+) 405.3 (M+H).

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Patent 2024
1H NMR Charcoal Chromatography ethyl acetate Heptanes Pyrimidines Sulfoxide, Dimethyl
This study was conducted in Damietta Governorate on the Egyptian Mediterranean coast (northern east Nile Delta), Egypt through the period from October 2021 to March 2022. A total of 200 cloacal swabs were collected from migratory and broiler chicken birds. Broiler chickens were selected from poultry farms and live bird markets near which the migratory birds were hunted at the similar time points. One hundred samples were obtained from migratory birds and 100 from broiler chickens; 50 from 5 poultry farms (10 for each farm) with deep litter system and 50 from 3 live bird markets located in different regions inside Damietta Governorate. Five broiler poultry farms were chosen on the basis of their owners’ willingness to permit the samples collection. Broiler chicken birds from the farms and live bird markets were selected randomly. The map of Damietta Governorate was constructed to highlight the location of the selected broiler chicken farms and live bird markets in relation to the rest of Damietta (Supplementary Fig. 9). The migratory birds that were found near to the examined farms and live bird markets were trapped by net traps, sampled, marked (to ensure that each bird was only sampled once) and photographed to detect its species. The cotton swabs were aseptically collected on 2 ml of Bolton broth (Oxoid, UK) then labeled and transported within 1 h in an ice box at 4 °C to the Reference Laboratory for Veterinary Quality control on Poultry production to perform further examinations. All samples were incubated at 42 °C for 48 h under microaerophilic conditions. Isolation and identification of Campylobacter spp.
Each enriched sample was streaked onto modified charcoal cefoperazone deoxycholate agar (Oxoid, UK) with antibiotic solution (cefoperazone sodium salt; 0.032 g, amphotericin B; 0.01 g and water; 5 ml) and incubated at 42 °C for 48 h. The suspected colonies were identified by morphological characteristics and Gram staining [45 ]. The suspected isolates were subjected to standard biochemical procedures, including tests for hippurate, acetate hydrolysis and catalase [46 ].
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Publication 2023
Acetate Agar Amphotericin B Antibiotics Aves Campylobacter Catalase Cefoperazone Charcoal Chickens Deoxycholate Enterobacter Fowls, Domestic Gossypium Hartnup Disease hippurate Hydrolysis isolation Physical Examination Sodium, Cefoperazone Specimen Collection
HESCs were grown in DMEM/F12 medium without phenol red (Sigma-Aldrich, St. Louis, MO, United States of America), added with 10% charcoal dextran-treated fetal bovine serum (FBS; HyClone Laboratories, Inc., Logan, UT, United States of America), 1% ITS - Premix (BD Biosciences, San Jose, CA, United States of America) and 5 ng/mL puromycin (Thermo Fisher Scientific, Ottawa, ON, CAN). Every culture was kept at 37 °C in an incubator with 5% CO2. HESCs were cultivated for a day after being seeded at a density of 4 × 105 cells per plate in 60-mm tissue culture dishes with full culture media. HESCs were treated with BMP2 (0, 10, 25, or 50 ng/ml) for the concentration-dependent research or with 25 ng/mL BMP2 for the time-course study after serum deprivation in DMEM/F12 media without FBS for 18 h. For the concentration-dependent investigation, cells were taken at 24 h, while for the time-course study, cells were taken at 3, 6, 12, 24 h, and 48 h.
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Publication 2023
BMP2 protein, human Cells Charcoal Culture Media Dextran Human Embryonic Stem Cells Hyperostosis, Diffuse Idiopathic Skeletal Puromycin Serum Tissues
Our samples for AMS-dating were obtained on short-lived organic material from secure and stratigraphically well-defined contexts. As secure contexts, we appraise archaeological assemblages that did not contain later archaeological material, i.e. ceramics that obviously intruded from later into earlier phases. Archaeologists involved in the excavation of multilayer settlements sites are aware of the appearance of residual material through reworking due to levelling and building activities, including the opening of pits. It was due to such activities that sparse pottery finds of Mycenaean type or origin appeared throughout the Early Iron Age stratigraphic sequence of Sidon. This applies in particular to our 14C-dated Phases C, D and E. It is not a coincidence that more than half of the Mycenaean and other Late Bronze Age pottery sherds from the site were found in just one room (Room 6), and this is the room that experienced the most extensive reworking. We also have instances of vessels that were reconstructed from sherds scattered throughout different phases. The large majority of the Early Iron Age contexts containing substantial residual ceramic material were not considered to have any value for the purpose of 14C-sampling.
To establish an absolute time-scale for Sidon Phases A-K we have at our disposal altogether 37 14C-ages on (annual-growth) olive stones and (short-lived) animal bones (Table 1). A first set of 14C-ages were processed in the year 2017 on 29 olive stones and 3 bones at the Oxford 14C-AMS laboratory (Lab Code: OxA). A second set of 14C-ages on 5 bones were processed in 2018 at the Mannheim 14C-AMS laboratory (Lab Code: MAMS). The majority of 14C-ages have standard deviations of ± 30 BP or better. According to the information provided by the laboratories, the bone collagen was extracted using weak acid dissolution, followed by ultrafiltration and separation of the fraction > 30 kD. The extracted organic carbon was then dry-frozen and burnt in an Elemental Analyser to produce CO2 which was catalysed to produce graphite. The charred olives were pre-treated using the standard ABA-method (Acid/Base/Acid; HCl/NaOH/HCl). By selectively dating olive stones (78%), whenever available, and with sampling extended to include short-lived animal bone (22%) when olive stones were not available, the idea is to avoid any kind of inbuilt ‘old wood’ effect that might be due to any perchance selection of inner tree-rings, reworked wood, or of recycled charcoal e.g. for domestic heating purposes. In consequence, potential outliers are most likely caused by stratigraphic reworking (olive stones), in addition to potential chemical alteration (bones).
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Publication 2023
Acids Animals Blood Vessel Bones Burns Calculi Carbon Charcoal Collagen Debility Freezing Graphite Iron Mammography Olea Olea europaea Trees Ultrafiltration Van der Woude syndrome
All the archaeological remains and samples collected during the excavation campaigns are currently stored at the Ministry of Culture of Peru, except for the micromorphological thin sections and the charcoal samples, which are stored at the Malher Centre (Paris, France) and the MSH Mondes (Nanterre, France) respectively.
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Publication 2023
Charcoal Microtomy

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Fetal Bovine Serum (FBS) is a cell culture supplement derived from the blood of bovine fetuses. FBS provides a source of proteins, growth factors, and other components that support the growth and maintenance of various cell types in in vitro cell culture applications.
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Penicillin/streptomycin is a commonly used antibiotic solution for cell culture applications. It contains a combination of penicillin and streptomycin, which are broad-spectrum antibiotics that inhibit the growth of both Gram-positive and Gram-negative bacteria.
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RPMI 1640 is a common cell culture medium used for the in vitro cultivation of a variety of cells, including human and animal cells. It provides a balanced salt solution and a source of essential nutrients and growth factors to support cell growth and proliferation.
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DMEM (Dulbecco's Modified Eagle's Medium) is a cell culture medium formulated to support the growth and maintenance of a variety of cell types, including mammalian cells. It provides essential nutrients, amino acids, vitamins, and other components necessary for cell proliferation and survival in an in vitro environment.
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Charcoal-stripped Fetal Bovine Serum (Charcoal-stripped FBS) is a specialized cell culture supplement. It is produced by treating Fetal Bovine Serum with activated charcoal to selectively remove hormones, growth factors, and other small lipophilic molecules.
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The LNCaP cell line is a human prostate adenocarcinoma cell line. It is a well-characterized in vitro model system for the study of prostate cancer.
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Penicillin is a type of antibiotic used in laboratory settings. It is a broad-spectrum antimicrobial agent effective against a variety of bacteria. Penicillin functions by disrupting the bacterial cell wall, leading to cell death.
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Lipofectamine 2000 is a cationic lipid-based transfection reagent designed for efficient and reliable delivery of nucleic acids, such as plasmid DNA and small interfering RNA (siRNA), into a wide range of eukaryotic cell types. It facilitates the formation of complexes between the nucleic acid and the lipid components, which can then be introduced into cells to enable gene expression or gene silencing studies.
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Streptomycin is a broad-spectrum antibiotic used in laboratory settings. It functions as a protein synthesis inhibitor, targeting the 30S subunit of bacterial ribosomes, which plays a crucial role in the translation of genetic information into proteins. Streptomycin is commonly used in microbiological research and applications that require selective inhibition of bacterial growth.
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RPMI 1640 medium is a commonly used cell culture medium developed at Roswell Park Memorial Institute. It is a balanced salt solution that provides essential nutrients, vitamins, and amino acids to support the growth and maintenance of a variety of cell types in vitro.

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Charcoal, a dark porous residue obtained by the heating of wood, peat, coconut shells, or other substances in the absence of air, has a variety of uses.
It can be used as a fuel, in purification processes, and in the production of various chemicals.
Charcoal is also used for medicinal purposes, such as in the treatment of poisoning and digestive disorders.
Researchers continue to explore the potential applications of charcoal, leveraging advanced technologies and methodologies to optimize its properties and unlock new possibilities.
Discover the latest advancements in charcoal research and development with PubCompare.ai, an AI-driven platform designed to enhance reproducibility and accuracy in your scientific inquiries.
Explore the use of charcoal in cell culture applications, such as Fetal Bovine Serum (FBS), Penicillin/Streptomycin, RPMI 1640, and DMEM media.
Learn how Charcoal-stripped FBS can be used to remove lipophilic compounds, and discover the potential of charcoal in cancer research with LNCaP cell lines.
Optimize your experiments with the help of Penicillin, Streptomycin, and Lipofectamine 2000 reagents.
Discover the future of charcoal optimization today!