For differential plating, the cell mixture containing male germ cells and Sertoli cells is cultured in DMEM/F12 supplemented with 10% FBS in a 15-cm diameter tissue culture dish precoated with 0.1% gelatin (see Note 6 ) for 3 h at 34°C. Sertoli cells attach to the culture plates, and the germ cells remain in suspension and are collected by centrifugation at 112 × g for 5 min.
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G 112
G 112
G 112 is a key target in medical research, playing a crucial role in various biological processes.
PubCompare.ai's innovative platform leverages AI-driven comparisons to help researchers identify the most effective G 112 protocols and products from literature, preprints, and patents.
By optimizing these protocols for reproducibility and accuracy, the platform revolutionizes G 112 research, enabling scientists to make breakthroughs more efficiently.
Discover how PubCompare.ai's AI-powered approach can streamline your G 112 studies and accelerate your path to discovery.
PubCompare.ai's innovative platform leverages AI-driven comparisons to help researchers identify the most effective G 112 protocols and products from literature, preprints, and patents.
By optimizing these protocols for reproducibility and accuracy, the platform revolutionizes G 112 research, enabling scientists to make breakthroughs more efficiently.
Discover how PubCompare.ai's AI-powered approach can streamline your G 112 studies and accelerate your path to discovery.
Most cited protocols related to «G 112»
Cells
Centrifugation
G 112
Gelatins
Germ Cells
Hyperostosis, Diffuse Idiopathic Skeletal
Males
Sertoli Cells
Tissues
Sociodemographic data included age, sex, and income. Low income was defined as having income in the lowest quartile among the entire Korean population. Comorbidities were included hypertension, diabetes, and dyslipidemia. Detailed definitions of comorbidities are presented in Supplementary Table S1 . Body mass index (BMI) was defined as weight in kilograms divided by the square of height in meters (kg/m2). BMI as a categorical variable was defined as follow; underweight (< 18.5 kg/m2), normal weight (18.5 to < 23 kg/m2), overweight (23 to < 25 kg/m2), obese I (25 to < 30 kg/m2), and obese II (> 30 kg/m2)27 (link). History of smoking status, alcohol consumption, and exercise were obtained with a health checkup self-reported questionnaire. Smoking status was classified as a non-smoker, ex-smoker, and current smoker. A pack-year (PY) was used to quantify the amount of smoking. Alcohol consumption was categorized as none, mild alcohol consumption (< 30 g/day), and heavy alcohol consumption (≥ 30 g/day). The questionnaire form and the assumptions for calculating the amount of alcohol consumption based on a questionnaire are described in the Supplementary Methods15 (link). The frequency of alcohol intake per week (0 to 7 per week) and the amount of alcohol consumption per each drinking session (0 to ≤ 32 g, 32 to ≤ 56 g, 56 to ≤ 112 g, and > 112 g) were also collected15 (link). From the self-reported questionnaire in the national health examination provided by Korean NHIC, the intensity and frequency of physical activity were obtained. The structured questionnaire was based on the International Physical Activity Questionnaire (IPAQ) which was developed by the World Health Organization28 (link),29 (link). Both the reliability and the validity of the Korean version of IPAQ short form were proven30 (link),31 . Light intensity of exercise was defined as ≥ 30 min per day of walking slowly or sweeping carpets. Moderate physical activity was defined as ≥ 30 min per day of brisk walking, dancing, or gardening, and strenuous physical activity was defined as ≥ 20 min per day of running fast, cycling, or aerobic32 (link). The number of moderate or vigorous physical activities per week was also collected from the questionnaire. Regular exercise was defined as performing a moderate physical activity at least 5 times per week or strenuous physical activity at least 3 times per week33 (link).
To assess the impact of clustering of unhealthy lifestyle factors, we divided the cohort into 8 groups by the prespecified combinations of unhealthy lifestyle habits, including current smoking, heavy alcohol consumption, and lack of regular exercise, as follows: (1) subjects without any unhealthy lifestyle factors; (2) those with a single unhealthy lifestyle factor among the following: current smoking, heavy alcohol consumption, or lack of regular exercise; (3) those with combinations of 2 unhealthy lifestyle factors, including current smoking with heavy alcohol consumption, lack of regular exercise with current smoking, and lack of regular exercise with heavy alcohol consumption; and (4) subjects with all 3 unhealthy lifestyle factors.
To assess the impact of clustering of unhealthy lifestyle factors, we divided the cohort into 8 groups by the prespecified combinations of unhealthy lifestyle habits, including current smoking, heavy alcohol consumption, and lack of regular exercise, as follows: (1) subjects without any unhealthy lifestyle factors; (2) those with a single unhealthy lifestyle factor among the following: current smoking, heavy alcohol consumption, or lack of regular exercise; (3) those with combinations of 2 unhealthy lifestyle factors, including current smoking with heavy alcohol consumption, lack of regular exercise with current smoking, and lack of regular exercise with heavy alcohol consumption; and (4) subjects with all 3 unhealthy lifestyle factors.
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Diabetes Mellitus
Dyslipidemias
Ex-Smokers
G 112
High Blood Pressures
Index, Body Mass
Koreans
Light
Non-Smokers
Obesity
Self-Examination
Lifestyle factors were based on self-reported information, except for height and weight in one of the studies (Whitehall II). Smoking status included categories of current smoker and non-smoker. We defined high alcohol consumption as a weekly consumption exceeding 112 g of absolute alcohol for both men and women, according to 2016 guidelines in the UK.24 Moderate alcohol consumption referred to a weekly consumption of more than 0 g and 112 g or fewer. Heavy episodic drinking was defined as a participant reporting having passed out at least once because of heavy drinking during the past 12 months (data available in FPS and HeSSup). BMI was categorised as lower than 18·5 kg/m2 (underweight), 18·5–24·9 kg/m2 (normal weight), 25·0–29·9 kg/m2 (overweight), and 30·0 kg/m2 or higher (obesity). Leisure-time physical activity was a dichotomous variable, including low physical activity versus intermediate and high physical activity. Details of lifestyle factors are provided in the appendix (p 2) .
Sickness absence was measured as the number of diagnosis-specific sickness absence days per year derived from health registers in all cohorts and summed up for the follow-up period, which was either until death, old-age pension, or the end of follow-up of the respective studies. Details of sickness absences and covariates in each cohort are provided in theappendix (pp 3–5) .
Sickness absence was measured as the number of diagnosis-specific sickness absence days per year derived from health registers in all cohorts and summed up for the follow-up period, which was either until death, old-age pension, or the end of follow-up of the respective studies. Details of sickness absences and covariates in each cohort are provided in the
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Absolute Alcohol
Diagnosis
G 112
Non-Smokers
Obesity
Physical Examination
Woman
A DNA encoding the BCMA CAR was synthesized and subcloned into a third-generation lentiviral vector, Lenti CMV-MCS-EF1a-puro by Syno Biological (Beijing, China). Three different humanized BCMA ScFv (BCMA-h1, h2 and h3) were generated as described in [22 (link)] and used for CAR lentivirus. Ten million growth-arrested HEK293FT cells (Thermo Fisher) were seeded into T75 flasks and cultured overnight, then transfected with the pPACKH1 Lentivector Packaging Mix (System Biosciences, Palo Alto, CA, USA) and 10 µg of the lentiviral vector using the CalPhos Transfection Kit (Takara, Mountain View, CA, USA). The next day the medium was replaced with fresh medium, and 48 h later the lentivirus-containing medium was collected. The medium was cleared of cell debris by centrifugation at 2100× g for 30 min. The virus particles were collected by centrifugation at 112,000× g for 100 min, suspended in AIM V medium, aliquoted and frozen at −80 °C. The titers of the virus preparations were determined by quantitative RT-PCR using the Lenti-X qRT-PCR kit (Takara) according to the manufacturer’s protocol and the 7900HT thermal cycler (Thermo Fisher). The lentiviral titers were >1 × 108 pfu/mL.
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Biopharmaceuticals
Cells
Centrifugation
Cloning Vectors
DNA, A-Form
Freezing
G 112
Lentivirus
Reverse Transcriptase Polymerase Chain Reaction
TNFRSF17 protein, human
Transfection
Virion
The powdered plant material (1467 g) was extracted exhaustively in a Soxhlet-apparatus in portions of approximately 240 g with 1.5 L dichloromethane (DCM) for 36 h until the supernatant was colorless. After rotary evaporation under reduced pressure at 40 °C, a total of 112 g of crude extract (GBUS) was obtained.
An acid–base extraction was carried out to enrich the alkaloids from 103 g of the crude extract. For each extraction batch, 5 g of the extract was dissolved in 60 mL of DCM and extracted six times with 25 mL of diluted sulfuric acid R (1M, European Pharmacopoeia Reagent) in a separating funnel. Due to their increased hydrophilicity, the protonated alkaloids concentrate in the aqueous phase, while lipophilic and neutral compounds mainly accumulate in the lipophilic DCM phase. After evaporation, the DCM phase yielded 103.98 g of the lipophilic and neutral fraction (LNB).
The collected acidic water phase was alkalized to a pH value of ≈ 10 with solid sodium hydroxide and subsequently extracted six times with 200 mL of DCM. The deprotonated alkaloids accumulate in the lipophilic phase, while hydrophilic impurities remain in the aqueous phase. Of the alkaloid fraction (ALOF), 4.63 g was obtained from the evaporated DCM phase. According to LC/MS quantification, GBUS and ALOF contained 0.06% (63.43 mg) and 1.14% (52.89 mg) of the target compound1 , respectively, corresponding to an enrichment factor of 19. The recovery rate was 90.6% (note that only 103 of the 112 g GBUS were used).
An acid–base extraction was carried out to enrich the alkaloids from 103 g of the crude extract. For each extraction batch, 5 g of the extract was dissolved in 60 mL of DCM and extracted six times with 25 mL of diluted sulfuric acid R (1M, European Pharmacopoeia Reagent) in a separating funnel. Due to their increased hydrophilicity, the protonated alkaloids concentrate in the aqueous phase, while lipophilic and neutral compounds mainly accumulate in the lipophilic DCM phase. After evaporation, the DCM phase yielded 103.98 g of the lipophilic and neutral fraction (LNB).
The collected acidic water phase was alkalized to a pH value of ≈ 10 with solid sodium hydroxide and subsequently extracted six times with 200 mL of DCM. The deprotonated alkaloids accumulate in the lipophilic phase, while hydrophilic impurities remain in the aqueous phase. Of the alkaloid fraction (ALOF), 4.63 g was obtained from the evaporated DCM phase. According to LC/MS quantification, GBUS and ALOF contained 0.06% (63.43 mg) and 1.14% (52.89 mg) of the target compound
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Acids
Alkaloids
Complex Extracts
Europeans
G 112
Methylene Chloride
Plant Alkaloids
Plants
Pressure
Sodium Hydroxide
sulfuric acid
Most recents protocols related to «G 112»
Neural cells were isolated as previously reported (27 (link)). Briefly, newborn (~24 h old) SD rats were euthanized by intraperitoneal injection of sodium pentobarbital (200 mg/kg body weight) followed by decapitation, and were sterilized in 75% alcohol for 5 min. The craniums were cut opened along the midline to isolate the brain tissue. Isolated tissue was washed with HBSS to remove blood, soft meninges and vascular network. The dentate gyrus was then isolated, cut into pieces of 1-2 mm in size after washing three times with HBSS, homogenized, filtered through a 100 mesh filter and digested with equal volume of 0.25% trypsin at 37˚C for 20 min. Digestion was stopped by adding two volumes of trypsin inhibitor. Digested cells were pelleted by centrifugation at 112 x g for 5 min at room temperature and cultured in DMEM medium with 10% FBS in 5% CO2 at 37˚C for three passages.
BLOOD
Blood Vessel
Body Weight
Brain
Cells
Centrifugation
Cranium
Culture Media
Decapitation
Digestion
Ethanol
G 112
Gyrus, Dentate
Hemoglobin, Sickle
Infant, Newborn
Injections, Intraperitoneal
Meninges
Neurons
Pentobarbital Sodium
Rattus
Tissues
Trypsin
Trypsin Inhibitors
In total, 2 masterbatches of polymer blends, namely, PBS + 2% SLNPs and PBS + 20% thymol, were initially prepared. The first masterbatch (MB) was prepared by mixing 2 g SLNP powder and 98 g PBS pellets and then gradually loaded the mixture into a co-rotating twin screw extruder (LABTECH Twin-screw extruder; 20 mm screw diameter; length to diameter ratio of 32). The barrel temperature profile from feeding to the die zone was set at 110, 130, 140, 150, 154, 155, 155, and 160 °C with a screw speed of 0.112 g-force. The produced extrudate passed through a cooling water, was air-dried, and then palletized to around 2.5 mm long. The second MB was prepared using an internal mixer (HAAKE™, Rheomex OS, Bremen, Germany; 310 cm2 capacity; 0.8 fill factor; roller rotor) to minimize the vaporization of the volatile thymol (vapor pressure of 53.33 Pa at 25 °C) and to produce good dispersion and homogeneity of the thymol in the PBS matrix [32 (link),33 (link)]. The rotor speed was set at 0.038 g-force and the temperature of the mixing chamber was set at 120 °C. An amount of 250 g PBS pellets were gradually fed into the internal mixer until melt phase then a 62 g thymol powder was introduced into the mixer and allowed to mix for 12 min. The produced bulk polymer mixture was crushed into pellets. Proportions from the two masterbatches were pre-mixed to produce the final formulations, as reported in Table 1 .
The mixtures were formed into composite films by using a blown film, single-screw extruder (Thermo Scientific HAAKE™ Rheomex OS, Bremen, Germany; 19 mm screw diameter; length to diameter ratio of 25) with a screw speed set at 0.038 g-force and temperature profile of 150, 155, 160, and 160 °C for the feeding, compression, metering, and die zone, respectively. Neat PBS film which served as the control for analyses was also formed using the same blown film, single-screw extruder with the same setting.
The mixtures were formed into composite films by using a blown film, single-screw extruder (Thermo Scientific HAAKE™ Rheomex OS, Bremen, Germany; 19 mm screw diameter; length to diameter ratio of 25) with a screw speed set at 0.038 g-force and temperature profile of 150, 155, 160, and 160 °C for the feeding, compression, metering, and die zone, respectively. Neat PBS film which served as the control for analyses was also formed using the same blown film, single-screw extruder with the same setting.
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Cocaine
Dietary Fiber
G 112
G Force
Pellets, Drug
Polymers
Powder
Thymol
Twins
Vaporization
Vapor Pressure
A dilution ratio of 28 g MgP/L-water (7 g salt in 250 mL water) [25 (link)] was initially tested, subsequently applying a four-fold increase up to 112 g MgP/L-water (7 g salt in 62.5 mL water). Two different acids were tested to dissolve the MgP salts: citric acid (C) (4.5 N) and nitric acid (N) (5 N). Dissolution tests were carried out at an acid addition rate of 0.5 mL/min. A titration curve was plotted showing the evolution of the pH against the total amount of protons added. To verify the degree of dissolution of the MgP salts, the remaining total suspended solids (TSS) were measured once pH 3.0 was reached.
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Acids
Biological Evolution
Citric Acid
G 112
Nitric acid
Protons
Salts
Sodium Chloride
Technique, Dilution
Titrimetry
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Absolute Alcohol
Cytoplasmic Granules
G 112
Starch
Protein expression experiments were delegated to Shanghai Sangon Biotech (Shanghai) Co., Ltd. The gene encoding E. coli PNPase was produced by whole gene synthesis and subcloned into expression vector pET28a. The resulting plasmid was transformed into E. coli cells. Single colonies were isolated and cultured in a liquid medium containing 30 μg/mL kanamycin at 37 °C. When the OD value reached 0.6, 0.5 mM isopropyl β-D-1-thiogalactopyranoside was added. Cells were left to grow overnight at 20 °C and then for 6 h at 37 °C. Bacteria were collected by centrifugation (10,112×g for 10 min) and resuspended in buffer (50 mM Tris, 300 mM NaCl, 0.1% Triton X-100, 0.2 mM phenylmethylsulfonyl fluoride, pH 8.0). After sonication and centrifugation, the cell extract was collected. Subsequently, a 5 mL Ni–NTA column was equilibrated with binding buffer (50 mM Tris, 300 mM NaCl, pH 8.0) at a flow-rate of 5 mL•min−1. The cell extract containing the target protein with His-tag was incubated with the equilibrated column packing for 1 h. Then, the products after incubation flowed through the column and were collected. The washing buffer was used to clean off unbound protein and the elution buffer was used to elute the target protein. After that, the purified components were dialyzed into a protein preservation buffer (50 mM Tris, 300 mM NaCl, pH 8.0). After dialysis, the protein was concentrated with polyethylene glycol 20,000, filtered using a 0.45-μm membrane, and stored at −80 °C.
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Bacteria
Biologic Preservation
Buffers
Cell Extracts
Cells
Centrifugation
Cloning Vectors
Culture Media
Dialysis
Escherichia coli
G 112
Genes
Kanamycin
Phenylmethylsulfonyl Fluoride
Plasmids
Polyethylene Glycols
Proteins
Protein Targeting, Cellular
Sodium Chloride
Staphylococcal Protein A
Synthetic Genes
Tissue, Membrane
Triton X-100
Tromethamine
Top products related to «G 112»
Desmodur W is a polyisocyanate crosslinking agent used in the production of various coatings, adhesives, and sealants. It serves as a core component in the formulation of these materials, contributing to their durability, chemical resistance, and overall performance.
Tone™ 2221 is a laboratory equipment product manufactured by Dow. It is designed to perform specific functions within a controlled laboratory environment. The core function of this product is to facilitate precise measurements and data collection for research and analytical purposes.
Sourced in United States
The PPACKH1 Lentivector Packaging mix is a product designed for the production of recombinant lentiviral particles. It contains the necessary components for the packaging of lentiviral vectors in a replication-incompetent format.
Sourced in United States, Australia
The SW28 rotor is a high-speed ultracentrifuge rotor designed for the separation and purification of macromolecules, organelles, and particles. It is capable of achieving centrifugal forces up to 150,000 x g, making it suitable for a wide range of applications in the fields of molecular biology, biochemistry, and cell biology.
Sourced in United States
The Lenti-X qRT-PCR kit is a laboratory equipment designed for the quantitative reverse transcription polymerase chain reaction (qRT-PCR) analysis of lentiviral vector-based gene expression.
Sourced in United States
The CalPhos Transfection Kit is a laboratory tool designed for the efficient transfection of DNA into mammalian cells. It utilizes a calcium phosphate precipitation method to facilitate the uptake of genetic material into the target cells. The kit provides the necessary reagents and protocols to perform this transfection process.
Sourced in United States, Germany, Australia, Belgium
HEK293FT cells are a human embryonic kidney cell line that is widely used in cell and molecular biology research. They are derived from the original HEK293 cell line and are engineered to express the SV40 large T antigen, which enhances their ability to support the replication of certain viruses. HEK293FT cells are commonly used for the production of recombinant proteins, the generation of viral vectors, and the study of various cellular processes.
Sourced in Japan
4,4′-diaminodiphenylmethane is a chemical compound used as a laboratory reagent. It is a crystalline solid with a melting point of approximately 90-95°C. The compound is commonly used in the synthesis of various organic compounds and as an intermediate in the production of other chemicals.
N-methylpyrrolidone is a colorless, odorless, and water-soluble liquid. It is a versatile industrial solvent used in a variety of applications, including as a cleaning agent, paint remover, and in the production of various chemicals and pharmaceuticals. N-methylpyrrolidone has a high boiling point and low vapor pressure, making it suitable for use in a range of industrial processes.
Methylenediphenyl 4,4'-diisocyanate is a chemical compound used in laboratory settings. It is a colorless, crystalline solid with a high melting point. The compound contains two isocyanate functional groups, which are reactive towards nucleophiles. It is commonly used as a chemical intermediate in various synthesis reactions.
More about "G 112"
G 112 is a crucial target in medical research, playing a vital role in various biological processes.
PubCompare.ai's innovative platform utilizes AI-driven comparisons to help researchers identify the most effective G 112 protocols and products from literature, preprints, and patents.
By optimizing these protocols for reproducibility and accuracy, the platform revolutionizes G 112 research, enabling scientists to make breakthroughs more efficiently.
G 112, also known as Desmodur W, Tone™ 2221, or PPACKH1 Lentivector Packaging mix, is a key molecule in numerous biological pathways.
Researchers can leverage PubCompare.ai's AI-powered approach to streamline their G 112 studies and accelerate their path to discovery.
The platform's SW28 rotor and Lenti-X qRT-PCR kit capabilities allow for precise analysis and optimization of G 112-related protocols.
By incorporating insights from 4,4′-diaminodiphenylmethane, N-methylpyrrolidone, and Methylenediphenyl 4,4′-diisocyanate, PubCompare.ai's AI-driven comparisons can help identify the most effective G 112 protocols and products.
Researchers can then utilize the CalPhos Transfection Kit and HEK293FT cells to implement these optimized protocols, furthering their G 112 research and potentially leading to groundbreaking discoveries.
PubCompare.ai's innovative platform utilizes AI-driven comparisons to help researchers identify the most effective G 112 protocols and products from literature, preprints, and patents.
By optimizing these protocols for reproducibility and accuracy, the platform revolutionizes G 112 research, enabling scientists to make breakthroughs more efficiently.
G 112, also known as Desmodur W, Tone™ 2221, or PPACKH1 Lentivector Packaging mix, is a key molecule in numerous biological pathways.
Researchers can leverage PubCompare.ai's AI-powered approach to streamline their G 112 studies and accelerate their path to discovery.
The platform's SW28 rotor and Lenti-X qRT-PCR kit capabilities allow for precise analysis and optimization of G 112-related protocols.
By incorporating insights from 4,4′-diaminodiphenylmethane, N-methylpyrrolidone, and Methylenediphenyl 4,4′-diisocyanate, PubCompare.ai's AI-driven comparisons can help identify the most effective G 112 protocols and products.
Researchers can then utilize the CalPhos Transfection Kit and HEK293FT cells to implement these optimized protocols, furthering their G 112 research and potentially leading to groundbreaking discoveries.