The largest database of trusted experimental protocols
> Objects > Food > Cereals

Cereals

Cereals are a group of grasses cultivated for their edible grains or seeds, which are important food sources for humans and animals.
This category includes major cereal crops such as wheat, rice, corn, barley, oats, and rye, as well as minor cereals like millet and sorghum.
Cereals are rich in carbohydrates, proteins, vitamins, and minerals, making them a dietary staple worldwide.
Researching cereals can provide insights into their nutritional profiles, cultivation techniques, and potential health benefits.

Most cited protocols related to «Cereals»

The FFQ, originally developed for the TLGS, was a Willett-format questionnaire modified based on Iranian food items25 and contains questions about average consumption and frequency for 168 food items during the past year.7 The food items were chosen according to the most frequently consumed items in the national food consumption survey in Iran.25 Because different recipes are used for food preparation, the FFQ was based on food items rather than dishes, eg, beans, different meats and oils, and rice. Subjects indicated their food consumption frequencies on a daily basis (eg, for bread), weekly basis (eg, for rice and meat), monthly basis (eg, for fish), yearly basis (eg, for organ meats), or a never/seldom basis according to portion sizes that were provided in the FFQ. For each food item on the FFQ, a portion size was specified using USDA serving sizes (eg, bread, 1 slice; apple, 1 medium; dairy, 1 cup) whenever possible; if this was not possible, household measures (eg, beans, 1 tablespoon; chicken meat, 1 leg, breast, or wing; rice, 1 large, medium, or small plate) were chosen. Table 1shows food items and portion sizes used in the FFQ. Trained dietary interviewers with at least 3 of experience in the Nationwide Food Consumption Survey project25 or TLGS26 (link) administered the FFQs and 24-hour DRs during face-to-face interviews. The interviewer read out the food items on the FFQ, and recorded their serving size and frequency. The interview session took about 45 minutes. The interviewer for FFQ1 and FFQ2 was the same for each participant. Daily intakes of each food item were determined based on the consumption frequency multiplied by the portion size or household measure for each food item.27 The weight of seasonal foods, like some fruits, was estimated according to the number of seasons when each food was available.
Dietary data were also collected monthly by means of twelve 24-hour DRs that lasted for 20 minutes on average. For all subjects, 2 formal weekend day (Thursday and Friday in Iran) and 10 weekdays were recalled. All recall interviews were performed at subjects’ homes to better estimate the commonly used household measures and to limit the number of missing subjects. Detailed information about food preparation methods and recipe ingredients were considered by interviewers. To prevent subjects from intentionally altering their regular diets, participants were informed of the recall meetings with dietitians during the evening before the interview. All recalls were checked by investigators, and ambiguities were resolved with the subjects. Mixed dishes in 24-hour DRs were converted into their ingredients according to the subjects’ report on the amount of the food item consumed, thus taking into account variations in meal preparation recipes. For instance, broth or soup ingredients—usually vegetables (carrot or green beans), noodles, barley, etc.—differed according to subjects’ meal preparation. Because the only available Iranian food composition table (FCT)28 analyzes a very limited number of raw food items and nutrients, we used the USDA FCT29 as the main FCT; the Iranian FCT was used as an alternative for traditional Iranian food items, like kashk, which are not included in the USDA FCT.
The food items on the FFQ and DR were grouped according to their nutrient contents, based on other studies,30 (link) and modified according to our dietary patterns. Seventeen food groups were thus obtained, as follows: 1) whole grains, 2) refined grains, 3) potatoes, 4) dairy products, 5) vegetables, 6) fruits, 7) legumes, 8) meats, 9) nuts and seeds, 10) solid fat, 11) liquid oil, 12) tea and coffee, 13) salty snacks, 14) simple sugars, 15) honey and jams, 16) soft drinks, and 17) desserts and snacks (Table 1). The 168 food items on the FFQ were allocated to these 17 food groups, and the amounts in grams of each item were summed to obtain the daily intake of each food group.
Full text: Click here
Publication 2010
Barley Bread Breast Carrots Cereals Chickens Coffee Dairy Products Diet Dietitian Eating Fabaceae Face Fishes Food Fruit Honey Households Hyperostosis, Diffuse Idiopathic Skeletal Interviewers Meat Mental Recall Monosaccharides Nutrients Nuts Oryza sativa Plant Embryos Potato Raw Foods Snacks Sodium Chloride, Dietary Soft Drinks Vegetables Whole Grains
We created an overall plant-based diet index (PDI), a healthful plant-based diet index (hPDI), and an unhealthful plant-based diet index (uPDI). The procedure we used to create these indices is similar to the one used by Martínez-González et al. [13 (link)]; their “provegetarian food pattern” is similar in composition to our PDI. Frequencies of consumption of each food were converted into servings consumed per day. Then the number of servings of foods that belonged to each of 18 food groups were added up. The 18 food groups were created on the basis of nutrient and culinary similarities, within larger categories of animal foods and healthy and less healthy plant foods. We distinguished between healthy and less healthy plant foods using existing knowledge of associations of the foods with T2D, other outcomes (CVD, certain cancers), and intermediate conditions (obesity, hypertension, lipids, inflammation). Plant foods not clearly associated in one direction with several health outcomes, specifically alcoholic beverages, were not included in the indices. We also excluded margarine from the indices, as its fatty acid composition has changed over time from high trans fat to high unsaturated fat. We controlled for alcoholic beverages and margarine consumption in the analysis.
Healthy plant food groups included whole grains, fruits, vegetables, nuts, legumes, vegetable oils, and tea/coffee, whereas less healthy plant food groups included fruit juices, sugar-sweetened beverages, refined grains, potatoes, and sweets/desserts. Animal food groups included animal fats, dairy, eggs, fish/seafood, meat (poultry and red meat), and miscellaneous animal-based foods.
S1 Table details examples of foods constituting the food groups. The 18 food groups were divided into quintiles of consumption, and each quintile was assigned a score between 1 and 5. For PDI, participants received a score of 5 for each plant food group for which they were above the highest quintile of consumption, a score of 4 for each plant food group for which they were above the second highest quintile but below the highest quintile, and so on, with a score of 1 for consumption below the lowest quintile (positive scores). On the other hand, participants received a score of 1 for each animal food group for which they were above the highest quintile of consumption, a score of 2 for each animal food group for which they were between the highest and second highest quintiles, and so on, with a score of 5 for consumption below the lowest quintile (reverse scores). For hPDI, positive scores were given to healthy plant food groups, and reverse scores to less healthy plant food groups and animal food groups. Finally, for uPDI, positive scores were given to less healthy plant food groups, and reverse scores to healthy plant food groups and animal food groups. The 18 food group scores for an individual were summed to obtain the indices, with a theoretical range of 18 (lowest possible score) to 90 (highest possible score). The observed ranges at baseline were 24–85 (PDI), 28–86 (hPDI), and 27–90 (uPDI) across the cohorts. The indices were analyzed as deciles, with energy intake adjusted at the analysis stage.
Full text: Click here
Publication 2016
Alcoholic Beverages Animals Cereals Coffee Diet Eggs Fabaceae Fats Fats, Unsaturated Fatty Acids Feeds, Animal Fishes Food Fowls, Domestic Fruit Fruit Juices High Blood Pressures Inflammation Lipids Malignant Neoplasms Margarine Meat Nutrients Nuts Obesity Plants Plants, Edible Red Meat Seafood Solanum tuberosum Sugar-Sweetened Beverages Vegetable Oils Vegetables Whole Grains
We performed genomic breeding value estimation (GEBV) and hybrid prediction with wheat data, and the results were compared to other genomic selection and mixed model software, including rrBLUP [13 ], ASReml [21 ], regress (used by synbreed as well) [17 ,18 (link)], EMMREML [19 ], MCMCglmm [15 (link)], and BGLR [16 (link)]. We used the wheat data contained in the R package BGLR consisting of 599 inbred lines genotyped with 1279 diversity array technology (DArT) markers [16 (link)]. Phenotypic data consisted of grain yield (GY) for the 599 lines from the historical CIMMYT's Global Wheat Program evaluated in four mega-environments.
From the 599 wheat lines, 179,101 distinct single crosses can be performed. Kinship-based BLUP prediction for the 599 lines were obtained using rrBLUP (ridge regression), ASReml (average information), regress (Newton-Raphson), EMMREML (modified EMMA), BGLR (using the Reproducing kernel Hilbert space [RKHS] kernel), MCMCglmm (Gibbs sampling) and the three algorithms implemented in sommer (AI, EM, and EMMA). Similarity among BLUPs using all software was performed in R and displayed in tables and figures [26 ]. The genomic estimated breeding values (GEBV) for each of the 599 inbred lines was used to predict the performance of possible crosses as the average among the breeding value of the parental lines. The mixed model fitted has the form:
y=Xβ+Zu+ε
with variance:
V(y)=V(Zu+ε)=ZGZ+R
and the mixed model equations for this model are:
[XR1XXR1ZZR1XZR1Z+G1]1[XR1yZR1y]=[βu]
Here, G = Kσ2u, is the variance covariance matrix of the random effect u, from a multivariate normal distribution u ~ MVN(0, Kσ2u), K being, in the genomics context, the additive or genomic relationship matrix (A or Ag). X and Z are incidence matrices for fixed and random effects respectively, and R is the matrix for residuals (here Iσ2e). A mixed model with a single variance component other than the error (σ2e) can be used to estimate the genetic variance (σ2u) along with genotype BLUPs to exploit the genetic relationships between individuals coded in K (A). The genomic relationship matrix was constructed according to VanRaden where K = ZZ’/2Σpi(1-pi) [27 (link)]. Genotype BLUPs were calculated and considered equal to the GEBV and these were used to predict the performance of the 179,101 possible crosses as the average of parental genomic breeding values. We fitted this model using the sommer package by specifying the incidence and variance-covariance matrices and using the three algorithms implemented (AI, EM, EMMA). In addition, a five-fold cross validation was performed to calculate the predictive correlation for grain yield in the four mega environments available for the wheat data using the sommer package. In addition, heritability was estimated as h2 = σ2u / σ2u + σ2e.
Full text: Click here
Publication 2016
Cereals Genetic Diversity Genome Genotype Hybrids Parent Phenotype Reproduction Triticum aestivum
The integrated plant was modeled assuming a 1G raw material loading of 360,000 tons dry grain per year and a 2G raw material loading of 180,000 tons dry wheat straw per year. These raw material loadings correspond to an estimated annual ethanol production of 200,000 m3, assuming C6 fermentation only. In some of the simulated cases, C5 fermentation was also considered, which increased the annual ethanol production to approximately 230,000 m3. It was assumed that the plant was in operation 8000 h per year, and could be managed by 28 people. One 1G case and six integrated 1G + 2G cases were modeled. In the integrated cases, ethanol, DDGS, and biogas production from the C5 sugars were investigated, as well as biogas upgrading to vehicle fuel quality. A sensitivity analysis was also performed for the six integrated cases to assess variations in the biogas yield which increased the investigated configurations to another six supplementary cases.
An overview of the process is shown in Fig. 11, and further details are provided in Section “Case description” below.

Schematic overview of the 1G + 2G process and alternative configurations

Simulations were performed with the flow sheeting program Aspen Plus (version 8.2 from Aspen Technology Inc., Massachusetts, USA). Data for biomass components such as cellulose and lignin were retrieved from the National Renewable Energy Laboratory (NREL) database developed for biofuel components [28 ]. The NRTL-HOC property method was used for all units except in the heat and power production steam cycle, where STEAMNBS was used. The simulation models were further developments of previous work by Wingren et al. [29 (link), 30 (link)], Sassner and Zacchi [31 (link)] and Joelsson et al. [32 ]. Heat integration was implemented as described previously [32 ] using Aspen Energy Analyzer (version 8.2). The results from Aspen Plus were implemented in APEA, and were used together with vendors’ quotations to evaluate the capital and operational costs. Further details on the Aspen Plus modeling can be found in a previous publication [33 (link)].
Full text: Click here
Publication 2016
Biofuels Biogas Cellulose Cereals Ethanol Fermentation Hypersensitivity Lignin Plants Steam Sugars Triticum aestivum
Genotypic data was simulated consisting of 511 SNP markers in 40 inbred lines belonging to two heterotic groups (20 in each). Phenotypic data was simulated consisting of grain yield (GY) and plant height (PH) for the 40 parents and 100 out the 400 possible hybrids produced from the single-cross of both heterotic groups allowing for heterosis. Genotypes of the 40 parents were used to estimate the genomic relationship matrices as K = ZZ’/2Σpi(1-pi) [27 (link)] for both heterotic groups (K1 and K2), and the genomic relationship matrix for the 400 possible hybrids was obtained as the Kronecker product of the parental genomic relationship matrices K1K2 (K3). Given that the phenotypic data for the possible crosses was not masked, the hybrids were predicted by estimating the BLUPs for general combining abilities in males and females (GCAfemale, GCAmale) and specific combining abilities (SCA) of crosses along with their variance components (σ2GCA1, σ2GCA2, σ2SCA). The model has the form:
y=Xβ+Z1uGCA1+Z2uGCA2+Z3uSCA+ε
The mixed model equations for this model are:
[XR1XXR1Z1XR1Z2XR1Z3Z1R1XZ1R1Z1+G11Z1R1Z2Z1R1Z3Z2R1XZ2R1Z1Z2R1Z2+G21Z2R1Z3Z3R1XZ3R1Z1Z3R1Z2Z3R1Z3+G31]1[XR1yZ1R1yZ2R1yZ3R1y]=[βuGCA1uGCA2uSCA]
where β is the vector of fixed effects, uGCA1, uGCA2, uSCA are the BLUPs for GCAfemale, GCAmale, and SCA effects, X and Zs are incidence matrices for fixed and random effects respectively, R is the matrix for residuals (here Iσ2e), and G-11, G-12, G-13 are the inverse of the variance-covariance matrices for random effects. The BLUPs uGCA1, uGCA2, uSCA were used to predict the rest of the single-crosses as the sum of their respective GCA and SCA effects.
We fitted this model using the sommer package by specifying the incidence and variance-covariance matrices and using the AI and EM algorithms, given that EMMA method cannot estimate more than one variance component. The model could not be implemented in rrBLUP which is also limited to a single variance component. In the BGLR package the Reproducing kernel Hilbert space [RKHS] kernel was used, in ASReml and MCMCglmm the ‘ginverse’ argument was used to specify the variance-covariance structures, and in the regress package the multiple random effects model using the ZKZ’ kernel was fitted. EMMREML uses a similar syntax than sommer. Results from other software were compared with sommer. In addition, a five-fold cross validation was performed to calculate the prediction accuracy for plant height and grain yield in this population.
In order to show the advantage of fitting a model including dominance (SCA) compared to a pure additive models (GCA) with respect to the prediction ability for species displaying heterotic effects, two additional models were fitted including only GCA effects; 1) both parents having the same variance component and 2) each parent from a different heterotic group having a different variance component:
G=[Kσu2]andG=[K1σu1200K2σu22]
Models were compared with respect to their prediction ability after 500 runs of a five-fold cross validation for plant height and grain yield. Models were fitted using sommer with the default AI algorithm. In addition, heritability for both trait was estimated as; h2 = (σ2GCA1 + σ2GCA2) / (σ2GCA1 + σ2GCA2 + σ2e).
Full text: Click here
Publication 2016
Cereals Cloning Vectors Females Genome Genotype Hybrids Males Parent Phenotype Plants Tracheophyta

Most recents protocols related to «Cereals»

Not available on PMC !

Example 11

Small molecule agonists of the Liver X Receptor (LXR) have previously been shown to increase Apo E levels. To investigate whether increasing Apo-E levels via LXR activation resulted in therapeutic benefit, assays were carried out to assess the effect of the LXR agonist GW3965 [chemical name: 3-[3-[N-(2-Chloro-3-trifluoromethylbenzyl)-(2,2-diphenylethyl)amino]propyloxy]phenylacetic acid hydrochloride) on Apo-E levels, tumor cell invasion, endothelial recruitment, and in vivo melanoma metastasis (FIG. 10). Incubation of parental MeWo cells in the presence of therapeutic concentrations of GW3965 increased expression of ApoE and DNAJA4 (FIGS. 10A and 10B). Pre-treatment of MeWO cells with GW3965 decreased tumor cell invasion (FIG. 10C) and endothelial recruitment (FIG. 10D). To test whether GW3965 could inhibit metastasis in vivo, mice were administered a grain-based chow diet containing GW3965 (20 mg/kg) or a control diet, and lung metastasis was assayed using bioluminescence after tail-vein injection of 4×104 parental MeWo cells into the mice (FIG. 10E). Oral administration of GW3965 to the mice in this fashion resulted in a significant reduction in in vivo melanoma metastasis (FIG. 10E).

Full text: Click here
Patent 2024
Administration, Oral agonists Apolipoproteins E Cardiac Arrest Cells Cereals Diet Endothelium GW 3965 Liver X Receptors Lung Malignant Neoplasms Melanoma Mus Neoplasm Invasiveness Neoplasm Metastasis Parent phenylacetic acid Tail Veins

Example 4

Testing to evaluate hard water tolerance of exemplary formulations of a high-foaming, higher alkaline chlorinated cleaner (with and without PSO) was conducted to determine the impact of the PSO on hard water tolerance. The evaluated formulations are shown below in Table 8 wherein alkaline cleaning compositions including hydroxide alkalinity sources were combined with the PSO adducts and compared to the formulations without the PSO adducts (Control).

TABLE 8
EXP 9Control
DI water25-5025-50
NaOH 50%10-3010-30
PSO adducts, 40%1-5 0
Lauryl dimethylamine oxide 30% 5-10 5-10
Sodium Hypochlorite, 10%20-4020-40
Additional Functional Ingredients 5-10 5-10
100.00100

The hardness tolerance testing of the EXP 9 formulation and the control were conducted using 1% solutions in water with varying degrees of synthetic hardness created by adding various amounts of dissolved CaCl2) and MgCl2 to a combination of deionized water and NaHCO3. Once the solutions reached 140° F. they were removed from the heat and let stand for 30 minutes. A failure was characterized by the presence of visible flocculent after the 30 minutes, whereas a passing evaluation was characterized by the absence of visible flocculent after the 30 minutes. The results are shown in Table 9.

TABLE 9
Grains per
Water sourcegallonEXP 9Control
Synthetic hard water16PassPass
Synthetic hard water17PassPass
Synthetic hard water18PassFail
Synthetic hard water19PassFail
Synthetic hard water20Fail
Synthetic hard water21Fail
Synthetic hard water22Fail
Synthetic hard water23Fail

As shown in Table 10, the exemplary high-foaming formulation (EXP 9) according to the invention containing the PSO adducts had increased hard water tolerance over cleaning compositions not containing the PSO adducts.

The inventions being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the inventions and all such modifications are intended to be included within the scope of the following claims.

Full text: Click here
Patent 2024
Acids Alkalies Bicarbonate, Sodium Cereals dodecyldimethylamine oxide hydroxide ion Immune Tolerance Magnesium Chloride Sodium Hypochlorite
Not available on PMC !

Example 3

FIG. 8 is a photograph illustrating the microstructure of an example alloy composition including an iron nitride foil, with an average grain size of 8±1.5 μm. The example alloy composition of FIG. 8 was prepared using melt spinning. The composition had a coercivity of 200 Oe. The grains were relatively large, and ferromagnetically coupled.

Example 4

FIG. 9 is a photograph illustrating the microstructure of an example alloy composition including an iron nitride foil, with an average grain size of 6±1.3 μm. The example alloy composition of FIG. 9 was prepared using melt spinning. The composition had a coercivity of 2037 Oe. The grain boundaries were thicker compared to the grains of the example alloy composition of Example 3, and the ferromagnetic grains were separated by non-magnetic material.

Full text: Click here
Patent 2024
Alloys Cereals Iron
Not available on PMC !

Example 6

A sample alloy composition including a plurality of grains with a predetermined average grain size may be prepared according to the present prophetic example. Pure iron foil, for example, having a thickness of between about 1 μm to about 1 cm, is used as a precursor. The iron foil is heated at a temperature between about 650° C. and about 1600° C. for a period of time between about 0.5 hours and about 10 hours, followed by quenching in a liquid medium. The liquid medium includes cold water, brine, oil, liquid nitrogen, or liquid CO2. A grain structure associated with an average grain size between about 20 nm and about 100 nm is formed. The sample is nitrided using ammonia, at a temperature between about 120° C. and about 500° C., subject to a pressure between about 1 atmosphere and about 100 atmospheres. The nitride sample is annealed by a strained workpiece technique.

Full text: Click here
Patent 2024
Alloys Ammonia Atmosphere Atmospheric Pressure brine Cereals Cold Temperature Iron Nitrogen

Example 1

Recycled glass cullet is cleaned, ground to less than 150 micrometers (US Standard sieve size No. 100), mixed with a foaming agent (e.g., a carbonate foaming agent) in a pug mill, heated, and allowed to fragment from temperature shock. The resulting lightweight-foamed glass aggregates are cellular. After sample preparation, the initial moisture content is measured following ASTM D2216 (2010), grain size distributions are determined following ASTM C136/136M (2006) and the initial bulk density is measured following ASTM C127 (2012a) on the lightweight-foamed glass aggregates. The average moisture content is determined to be 1.06% and the average bulk density is determined to be 227.2 kg/m3 (14.2 pcf). Sieve analyses are performed following the dry sieving method on the lightweight-foamed glass aggregates. Particle size ranges from 10 to 30 mm (0.39 to 1.18 in) but is a very uniformly graded material.

Full text: Click here
Patent 2024
Carbonates Cells Cereals Dietary Fiber Shock

Top products related to «Cereals»

Sourced in United States, Austria, Japan, Belgium, United Kingdom, Cameroon, China, Denmark, Canada, Israel, New Caledonia, Germany, Poland, India, France, Ireland, Australia
SAS 9.4 is an integrated software suite for advanced analytics, data management, and business intelligence. It provides a comprehensive platform for data analysis, modeling, and reporting. SAS 9.4 offers a wide range of capabilities, including data manipulation, statistical analysis, predictive modeling, and visual data exploration.
Sourced in United States, China, Japan, Germany, United Kingdom, Canada, France, Italy, Australia, Spain, Switzerland, Netherlands, Belgium, Lithuania, Denmark, Singapore, New Zealand, India, Brazil, Argentina, Sweden, Norway, Austria, Poland, Finland, Israel, Hong Kong, Cameroon, Sao Tome and Principe, Macao, Taiwan, Province of China, Thailand
TRIzol reagent is a monophasic solution of phenol, guanidine isothiocyanate, and other proprietary components designed for the isolation of total RNA, DNA, and proteins from a variety of biological samples. The reagent maintains the integrity of the RNA while disrupting cells and dissolving cell components.
Sourced in United Kingdom, Germany, France, United States, Canada
The Mastersizer 2000 is a laser diffraction particle size analyzer that measures the size distribution of particles in a sample. It uses the principle of laser light scattering to determine the particle size distribution of materials in the range of 0.1 to 2000 microns.
Sourced in Germany, United States, Japan, United Kingdom, China, France, India, Greece, Switzerland, Italy
The D8 Advance is a versatile X-ray diffractometer (XRD) designed for phase identification, quantitative analysis, and structural characterization of a wide range of materials. It features advanced optics and a high-performance detector to provide accurate and reliable results.
Sourced in United States, Austria, Japan, Cameroon, Germany, United Kingdom, Canada, Belgium, Israel, Denmark, Australia, New Caledonia, France, Argentina, Sweden, Ireland, India
SAS version 9.4 is a statistical software package. It provides tools for data management, analysis, and reporting. The software is designed to help users extract insights from data and make informed decisions.
Sourced in Denmark, United States, Sweden, China
The Infratec 1241 Grain Analyzer is a laboratory equipment product designed for the analysis of various grain samples. It utilizes near-infrared (NIR) spectroscopy technology to determine the chemical composition and quality parameters of grains.
Sourced in Germany, United States, United Kingdom, Canada, China, Spain, Netherlands, Japan, France, Italy, Switzerland, Australia, Sweden, Portugal, India
The DNeasy Plant Mini Kit is a lab equipment product designed for the isolation and purification of DNA from plant samples. It utilizes a silica-based membrane technology to extract and concentrate DNA effectively from a variety of plant materials.
Sourced in Japan, United States, China, Germany, United Kingdom, Spain, Canada, Czechia
The S-4800 is a high-resolution scanning electron microscope (SEM) manufactured by Hitachi. It provides a range of imaging and analytical capabilities for various applications. The S-4800 utilizes a field emission electron gun to generate high-quality, high-resolution images of samples.
Sourced in Germany
The Quadrumat Junior mill is a laboratory-scale mill designed for the milling of small grain samples. It is used for grinding and reducing the particle size of various materials, such as cereals, grains, and other solid materials, in preparation for further analysis or processing.
Sourced in Ireland, United States
The Total Starch Assay Kit is a laboratory equipment product designed for the quantitative determination of total starch content in a variety of sample types, including food, feed, and other materials. The kit provides a reliable and accurate method for measuring the total starch present in a sample.

More about "Cereals"

Cereals, a key dietary staple, are a diverse group of grasses cultivated for their edible grains or seeds.
This category encompasses major cereal crops like wheat, rice, corn, barley, oats, and rye, as well as minor varieties such as millet and sorghum.
Cereals are renowned for their rich nutritional profiles, providing abundant carbohydrates, proteins, vitamins, and minerals that make them a global food source for both humans and animals.
Researching cereals can yield valuable insights into their cultivation techniques, processing methods, and potential health benefits.
Analytical tools like the Infratec 1241 Grain Analyzer and the Quadrumat Junior mill can be used to assess the physical and chemical properties of cereal grains.
Molecular techniques, such as the DNeasy Plant Mini Kit and the Total Starch Assay Kit, enable researchers to delve into the genetic and biochemical composition of these crops.
Platforms like PubCompare.ai can further enhance the research process by leveraging artificial intelligence to streamline the identification and comparison of effective cereal products and protocols.
Whether you're interested in enhancing cereal cultivation, optimizing processing methods, or exploring the nutritional and health aspects of these versatile grains, a wealth of information and tools are available to support your cereal research endeavors.
By staying up-to-date with the latest advancements in this field, you can contribute to the ongoing progress in cereal science and technology.