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Vitamins

Vitamins are a diverse group of organic compounds that are essential for normal physiologic function in humans and animals.
They cannot be synthesized by the body in sufficient amounts and must be obtained from the diet.
Vitamins are required in small amounts for a variety of metabolic processes and have important roles in maintaining health and preventing disease.
Deficiencies in specific vitamins can lead to a range of clinical disorders.
Vitamjns are commonly classified into two main types: fat-soluble (A, D, E, K) and water-soluble (B-complex, C).
Research on vitamins is crucial for understanding their effects on human health and developing optimal supplementation strategies.

Most cited protocols related to «Vitamins»

Using a FFQ, participants reported the intake of foods consumed during the previous month. The FFQ was designed for the Dutch population and based on the VetExpress, a 104-item FFQ, valid for estimating the intake of energy, total fat, saturated (SFA), monounsaturated (MUFA), and polyunsaturated fatty acids (PUFA), and cholesterol in adults [5 (link)]. The VetExpress was updated and extended with vegetables, fruit, and foods for estimating the intake of specific PUFA’s, vitamins, minerals, and flavonoids. To identify relevant foods and food groups for this questionnaire, food consumption data of the Dutch National Food Survey of 1998 were used. Foods that contributed >0.1% to the intake of one of the nutrients of interest of adults were added in this survey. Thus, the FFQ is expected to include foods that cover the daily intake of each nutrient of food of interest for at least 90%. In a final step, foods were clustered to food items and extended with new foods on the market and foods to guarantee face validity. The FFQ was sent to each study participant, and after completing it, the participants returned the FFQ in an envelope free of postal charge. A dietician went through each FFQ to check for completeness. If necessary, she contacted the participants by telephone and obtained information on unclear or missing items. The FFQ also included questions on adherence to a special diet as well as questions about the use of dietary supplements.
Some of the offspring and their partners who completed the general questionnaire of the LLS were invited to the clinic for additional measurements at the Leiden University Medical Center. These measurements lasted a half day and couples were invited for the morning program or the afternoon program, which were slightly different due to practical reasons. The first 24-hour recall was performed in those participants who came to the clinic for the measurement in the morning program [N=128 (Noffspring=62, Ncontrol=66)]. A dietician asked the participants about their dietary intake of the previous day covering all foods and beverages consumed from waking up until the next morning. The dieticians received standardized training, using a formal protocol, to reduce the impact of the interview on the reporting process. For the two remaining recalls, the dietician contacted the participants by telephone within the next seven days. The 24-hour recalls were performed throughout the year and the days were chosen non-consecutively. They include a randomly assigned combination of days of the week with all days of the week represented (80% weekdays and 20% weekend days), for each individual.
The food data from both dietary assessment methods were converted into energy and nutrient intake by using the NEVO food composition database of 2006 [6 ]. Furthermore, foods were categorized into 24 major food groups. Age was calculated from date of birth and completion date of the FFQ. For subjects with missing information on the date of completing the FFQ, we used the median date of the other subjects.
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Publication 2013
Adult Beverages Birth Cholesterol Diet Dietary Supplements Dietitian Eating Flavonoids Food Fruit Mental Recall Minerals Nutrient Intake Nutrients Polyunsaturated Fatty Acids Vegetables Vitamins
The prototrophic S. cerevisiae strains CEN.PK113-7D [21 ] and S288C (ATCC 204508) [82 (link)] were grown in liquid cultures. The shake-flask cultivations with biotin were performed in 500 ml flasks containing 100 ml of medium, which were incubated at 30°C on an orbital shaker set at 200-rpm. The composition of the synthetic medium (SM) was as follows: glucose (20 g.l-1), (NH4)2SO4 (5 g.l-1) KH2PO4 (3 g.l-1), MgSO4 (0.5 g.l-1), trace elements and vitamin solutions [62 (link)]. A separate biotin-free vitamin solution was used for growth in absence of biotin. The pH of the medium was adjusted to 5.0 and sterilized by autoclaving. Glucose was autoclaved separately. Vitamins were filter-sterilized and added to the medium. Growth of the various strains was monitored by OD measurements at 660 nm.
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Publication 2012
Biotin Glucose Strains Sulfate, Magnesium Trace Elements Tremor Vitamins
To investigate the determinants of cardiovascular diseases and other chronic conditions in Central and Eastern Europe, we are conducting a prospective cohort study in Russia, Poland, the Czech Republic and Lithuania. The study will investigate the following specific hypotheses:
• Socioeconomic factors are key determinants of health in CEE/FSU; we will examine the pathways involved in their action, including factors hypothesised below.
• Psychosocial factors, both at individual and population level, are related to CVD and other non-communicable diseases.
• Low consumption of fresh fruits and vegetables and their nutrient biomarkers are associated with increased risk of CVD;
• Binge drinking and heavy alcohol consumption are related to all-cause mortality, CVD and injury;
• Elevated concentration of homocysteine and low levels of folate and related B vitamins are associated with increased risk of CVD;
• Interactions between different groups of risk factors, in particular between heavy drinking and folate deficiency, and between the MTHFR genotype and folate deficiency, are associated with CVD.
In addition to these specific hypotheses, the study will also investigate several more general questions:
• The role of childhood socioeconomic circumstances and biological markers of their effects, such as leg length and lung functions, in the risk of CVD and other conditions in adulthood;
• Biological, social, economic and psychosocial determinants of healthy ageing (cognitive function, physical functioning, and quality of life of elderly persons);
• Genetic predictors and non-conventional biomarkers of CVD and other chronic diseases.
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Publication 2006
Aged Biological Markers Biopharmaceuticals Birth Cardiovascular Diseases Chronic Condition Cognition Disease, Chronic Folate Folic Acid Deficiency Fruit Genotype Homocysteine Injuries Methylenetetrahydrofolate Reductase Noncommunicable Diseases Nutrients Physical Examination Respiratory Physiology Vegetables Vitamins
The samples were classified into 24 different categories covering products from the plant kingdom, products from the animal kingdom and mixed food products. Information about sample processing (raw, cooked, dried etc), if any, was included, along with all sample specifications, i.e. product name, brand name, where the product/sample was procured and country of origin. The product information in the database was collected from the packing of the product, from supplier or purchaser. When this information was not available or the samples were handpicked, only country of origin is presented. Each sample is assigned to only one category. The classification was done according to information from the supplier or purchaser, or according to common traditional use of the food. Some foods may therefore be categorized otherwise in other food cultures. For products in the categories "Herbal/traditional plant medicine" and "Vitamin and dietary Supplements" some products may rightfully be classified as both an herbal medicine and a supplement, but are still assigned to only one category. All berries, fruits, and vegetables were fresh samples unless otherwise noted in the database. The Antioxidant Food Table contains 3139 samples. About 1300 of these samples have been published before [16 (link),17 (link),28 (link)] but for comparison and completeness we have included them in the present publication. All individual samples previously published are identified by a comment in the Antioxidant Food Table. The categories and products in the database are presented in alphabetic order. Information about brand names and product trademarks does not imply endorsement by the authors, and are reported as descriptive information for research applications only. The Antioxidant Food Table will in the future be available online as a searchable database. In addition to the products mentioned in this paper, other foods will in the future be analyzed and incorporated into the online version, which will be posted on the University of Oslo's web site.
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Publication 2010
Animals Antioxidants Berries Dietary Supplements Food Fruit Medicinal Herbs Plants Reproduction Vegetables Vitamins Volition
Trained interviewers administered the two-part telephone interview (CATI1 and CATI2) in either English or Spanish. The interview, which took about 2 h to complete overall, collected information on breast cancer risk factors, residential history, medical history, lifetime occupational history, reproductive history, socioeconomic status, and other information, including sister history of breast cancer (https://sisterstudy.niehs.nih.gov/english/baseline.htm and Table S1). The questionnaires were longer than those in other cohort studies to allow for collection of information on commonly studied known and potential risk factors as well as to collect data on occupational and environmental exposures that were not being collected in most other prospective studies.
Environmental and occupational exposures of interest included but were not limited to chemicals previously identified as mammary carcinogens or endocrine disruptors (Bennett and Davis 2002 (link); Rudel et al. 2007 (link)) and shift work; we asked about history of working in industries and occupations where exposure to these factors was possible as well as exposures at home, such as pesticides, paints, or hobby materials, and gardening. In addition to the time of enrollment, questions focused on periods that may be relevant to breast cancer risk, including in utero and childhood exposures, particularly around menarche. Addresses for current, longest adult, and longest childhood residence have been geocoded for linkage with various GIS databases for environmental exposures, such as air pollution, and census data for socioeconomic and neighborhood factors.
Participants completed self-administered questionnaires on diet, personal care products, family history of cancer, and early-life exposures, including the participant’s mother’s exposures during her pregnancy with the participant. The food frequency questionnaire (Block 98) (Boucher et al. 2006 (link)) was supplemented with questions about cooking practices, dietary intake of phytoestrogens, childhood diet, vitamin supplements, and complementary and alternative medicines and practices.
Publication 2017
Adult Air Pollution Carcinogens Cardiac Arrest Diet Dietary Supplements Endocrine Disruptors Environmental Exposure Food Hispanic or Latino Interviewers Malignant Neoplasm of Breast Malignant Neoplasms Mammary Gland Maternal Exposure Menarche Occupational Exposure Pesticides Phytoestrogens Pregnancy Uterus Vitamins

Most recents protocols related to «Vitamins»

Not available on PMC !

Example 2

100 mg of the Sarcodon aspratus extracts according to the present invention;

an appropriate amount of a vitamin mixture;

70 μg of vitamin A acetate;

1.0 mg of vitamin E;

0.13 mg of vitamin B1;

0.15 mg of vitamin B2;

0.5 mg of vitamin B6;

0.2 μg of vitamin B12;

10 mg of vitamin C;

10 μg of biotin;

1.7 mg of nicotinic acid amide;

50 μg of folate;

0.5 mg of calcium pantothenate;

an appropriate amount of a mineral mixture;

1.75 mg of ferrous sulfide;

0.82 mg of zinc oxide;

25.3 mg of magnesium carbonate;

15 mg of potassium phosphate monobasic;

55 mg of dicalcium phosphate;

90 mg of potassium citrate;

100 mg of calcium carbonate; and

24.8 mg of magnesium chloride.

The composition ratio of the vitamins and the mineral mixture described above may be determined according to a composition ratio used in general functional health foods, and the combination ratio of the vitamins and the mineral mixture may be arbitrarily determined. According to a conventional method of preparing functional health foods, these components are mixed, granules are prepared, and the granules are used to prepare a composition for a functional health food.

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Patent 2024
Ascorbic Acid Biotin Carbonate, Calcium Cobalamins Cytoplasmic Granules dicalcium phosphate ferrous sulfide Folate Functional Food magnesium carbonate Magnesium Chloride magnesium citrate Minerals Niacinamide Pantothenate, Calcium Potassium Potassium Citrate potassium phosphate retinol acetate Riboflavin Sarcodon aspratus Thiamine Vitamin A Vitamin B6 Vitamin E Vitamins Zinc Oxide

Example 6

This example provides a representative example of an aqueous solution to be used in a method described herein. The composition may contain the following ingredients:

5000 mcgcobalamin (vitamin B12)
200 mgascorbic acid (vitamin C)
 40 mgnicotinamide (vitamin B3)
 6 mgthiamine (vitamin B1)
 6 mgpyridoxine HCl (vitamin B6)
 3.6 mg riboflavin 5-phosphate sodium (vitamin B2)
 10 mgpantothenic acid (vitamin B5)
 0.1 mg Zinc sulfate heptahydrate
1 mlq.s., sterile water for injection

The aqueous solution is formulated in physiological saline and adjusted to about pH 7.4, thereby minimizing any injecting pain beyond the needle prick. In addition, the aqueous solution may be optionally supplemented with a preservative (e.g., benzyl alcohol), a chemical stabilizer (e.g., gentisic acid), and/or an additional bioactive agent (e.g., platelet-rich plasma) depending on anticipated delivery method, shelf-life, and intended effects.

Example 7

The purpose of this example is to evaluate the efficacy of a composition described herein in treating the signs of aging present on facial skin. A composition is prepared as in Example 6.

Two groups of human subjects (8-10 subjects per group) are injected with the composition or physiological saline (control) twice a day for a period of 29 days. At the end of the 29 day test period, the subjects are polled regarding various aspects of the effectiveness of the composition described herein in treating and/or minimizing signs of aging present on the skin. The following aspects of the composition described herein are evaluated:

    • (1) effectiveness of the composition described herein in improving the smoothness and/or softness of skin (i.e., making the skin feel smoother and softer following treatment);
    • (2) effectiveness of the composition described herein in improving the overall appearance of skin;
    • (3) effectiveness of the composition described herein in evening out skin tone and texture;
    • (4) effectiveness of the composition described herein in improving the clarity and/or radiance of skin;
    • (5) effectiveness of the composition described herein in making the skin look younger; and
    • (6) effectiveness of the composition described herein in making wrinkles appear softer and/or less prominent.
    • (7) effectiveness of the composition described herein in increasing the degree of hydration of the skin.

Patients treated with the composition exhibit improvement in one or more of the symptoms described herein.

Example 8

The purpose of this example is to evaluate the efficacy of a composition described herein in treating the signs of aging present on facial skin. A composition is prepared as in Example 6.

Two groups of human subjects (8-10 subjects per group) are injected with the composition or physiological saline (control) on days 1, 3, 7, 10, 14, 21, 30, 60, and 90 of treatment. At the end of the 90-day test period, the subjects are polled regarding various aspects of the effectiveness of the composition described herein in treating and/or minimizing signs of aging present on the skin. The following aspects of the composition described herein are evaluated:

    • (1) effectiveness of the composition described herein in improving the smoothness and/or softness of skin (i.e., making the skin feel smoother and softer following treatment);
    • (2) effectiveness of the composition described herein in improving the overall appearance of skin;
    • (3) effectiveness of the composition described herein in evening out skin tone and texture;
    • (4) effectiveness of the composition described herein in improving the clarity and/or radiance of skin;
    • (5) effectiveness of the composition described herein in making the skin look younger; and
    • (6) effectiveness of the composition described herein in making wrinkles appear softer and/or less prominent.
    • (7) effectiveness of the composition described herein in increasing the degree of hydration of the skin.

Patients treated with the composition exhibit improvement in one or more of the symptoms described herein.

While preferred embodiments have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the embodiments. It should be understood that various alternatives to the embodiments described herein may be employed. It is intended that the following claims define the scope of the embodiments and that methods and structures within the scope of these claims and their equivalents be covered thereby.

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Patent 2024
Ascorbic Acid Benzyl Alcohol Cobalamins Face Feelings gentisic acid Needles Niacin Niacinamide Obstetric Delivery Pain Pantothenic Acid Patients Pharmaceutical Preservatives physiology Platelet-Rich Plasma Pyridoxine Hydrochloride Riboflavin Saline Solution Skin Skin Pigmentation Sodium Riboflavin Phosphate Sterility, Reproductive Thiamine Vitamin B6 Vitamins Youth Zinc Sulfate, Heptahydrate

Example 14

Variables tested include: concentration of HA, concentration of zinc oxide, concentration of titanium dioxide, addition of vitamin C, and serum preparation method.

FIGS. 94A-94C are tables summarizing embodiments of cosmetic serums of the present disclosure with varying additives and concentrations of components suitable for protection against ultraviolet radiation (UV). Table 33 provides an embodiment of a hydrating serum of the present disclosure with vitamin C.

TABLE 33
Embodiment of Hydrating serum of
the present disclosure with vitamin C
% Silk Solution  1.0% w/v
(60 minute boil, 25 kDA)
Hyaluronic Acid 0.75% w/v
(sodium hyaluronate)
Lemongrass Oil20 uL/15 mL
silk solution
Sodium Ascorbyl Phosphate  6 g
Lactic Acid1.2 mL

A serum of the present disclosure can be made with from about 0.25% to about 10% sodium hyaluronate (increasing % results in more viscous serum). 0.5% to about 10% silk solutions can be used to prepare a serum of the present disclosure. A serum of the present disclosure can be clear and have a yellow tinted color. A serum of the present disclosure can have a pH=6. A serum of the present disclosure can have a lubricious texture that is rubbed in easily without residue.

Concentration of HA:

Hyaluronic acid (Sodium Hyaluronate) was tested as an ingredient in the UV silk serum due to its hygroscopic properties and widely accepted use in cosmetic products to promote hydration of skin. 1%, 2.5% and 5% HA solutions were tested. With increasing HA %, the serum became more viscous and gel like. 1% HA was not feasible for the UV serum due to the fact that the UV additives (zinc oxide, titanium dioxide) are not water soluble and need to be dispersed. 1% HA was not viscous enough for dispersion and the UV additives precipitated out. 2.5% gave the best consistency based on preferred feel, texture and viscosity and was able to disperse the UV additives. 5% was a very thick, viscous serum.

Concentration of Mineral Filters: Zinc Oxide and Titanium Dioxide:

Zinc oxide and titanium dioxide were explored as UV additives that are considered safe. These additives mechanically protect from UV radiation by forming a physical reflective barrier on the skin. Both are not soluble in water and must be dispersed for the current aqueous solution. Zinc oxide concentration varied from 2.5%, 3.75%, 5%, 5.625%, 10%, 12% and 15%. Titanium dioxide concentrations varied from 1.25%, 1.875%, 3%, 5% and 10%. Increasing the concentration of UV additives resulted in minor increases of white residue and how well dispersed the additives were, however if mixed well enough the effects were negligible. Zinc oxide and titanium dioxide were mixed together into serums in order to achieve broad spectrum protection. Zinc oxide is a broad spectrum UV additive capable of protecting against long and short UV A and UV B rays. However titanium dioxide is better at UV B protection and often added with zinc oxides for best broad spectrum protection. Combinations included 3.75%/1.25% ZnO/TiO2, 5.625%/1.875% ZnO/TiO2, 12%/3% ZnO/TiO2, 15%/5% ZnO/TiO2. The 3.75%/1.25% ZnO/TiO2 resulted in spf 5 and the 5.625%/1.875% ZnO/TiO2 produced spf 8.

Vitamin C:

Sodium ascorbyl phosphate was used as a vitamin C source. Formulations were created with the vitamin C concentration equal to that in the silk gel (0.67%). Formulations were also created with 20% sodium ascorbyl phosphate which is soluble in water.

Serum Preparation:

The vitamin C (sodium ascorbyl phosphate) must first be dissolved in water. Sodium hyaluronate is then added to the water, mixed vigorously and left to fully dissolve. The result is a viscous liquid (depending on HA %). The viscosity of the HA solution allows even dispersion of the zinc oxide and titanium dioxide and therefore HA must be mixed before addition of UV additives. The zinc oxide and titanium dioxide are then added to the solution and mixed vigorously with the use of an electric blender. Silk solution is then added and mixed to complete the serum formulation.

Chemical Filters:

A UV serum of the present disclosure can include one, or a combination of two or more, of these active chemical filter ingredients: oxybenzone, avobenzone, octisalate, octocrylene, homosalate and octinoxate. A UV serum of the present disclosure can also include a combination of zinc oxide with chemical filters.

In an embodiment, a UV serum of the present disclosure can be applied approximately 15 minutes before sun exposure to all skin exposed to sun, and can be reapplied at least every 2 hours. In an embodiment, a UV serum of the present disclosure includes water, zinc oxide, sodium hyaluronate, titanium dioxide, silk, and vitamin C or a vitamin C derivative such as sodium ascorbyl phosphate. In an embodiment, a UV serum of the present disclosure protects skin and seals in moisture with the power of silk protein. In an embodiment, a UV serum of the present disclosure improves skin tone, promotes collagen production and diminishes the appearance of wrinkles and fine lines with the antioxidant abilities of vitamin C. In an embodiment, a UV serum of the present disclosure delivers moisture for immediate and long-term hydration throughout the day with concentrated hyaluronic acid. In an embodiment, a UV serum of the present disclosure helps prevent sunburn with the combined action of zinc oxide and titanium dioxide. In an embodiment, a UV serum of the present disclosure is designed to protect, hydrate, and diminish fine lines while shielding skin from harsh UVA and UVB rays. In an embodiment, the silk protein in a UV serum of the present disclosure stabilizes and protects skin while sealing in moisture, without the use of harsh chemical preservatives or synthetic additives. In an embodiment, the vitamin C/derivative in a UV serum of the present disclosure acts as a powerful antioxidant that supports skin rejuvenation. In an embodiment, the sodium hyaluronate in a UV serum of the present disclosure nourishes the skin and delivers moisture for long-lasting hydration. In an embodiment, the zinc oxide and titanium dioxide in a UV serum of the present disclosure shields skin from harmful UVA and UVB rays. The silk protein stabilization matrix in a UV serum of the present disclosure protects the active ingredients from the air, to deliver their full benefits without the use of harsh chemicals or preservatives. The silk matrix also traps moisture within the skin furthering the hydrating effect of the sodium hyaluronate.

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Patent 2024
Acids Antioxidants Ascorbic Acid avobenzone Collagen Electricity Feelings Figs Furuncles homosalate Hyaluronic acid Minerals octinoxate octisalate octocrylene oxybenzone Pharmaceutical Preservatives Proteins Radiation Rejuvenation SERPINA3 protein, human Serum Serum Proteins Silk Skin Skin Pigmentation sodium ascorbyl phosphate Sodium Hyaluronate Strains Sunburn titanium dioxide Viscosity Vitamin A Vitamins west indian lemongrass oil Zinc Oxide
Not available on PMC !

Example 5

An aqueous solution containing the following ingredients:

    • about 1500 to about 6250 meg cobalamin (vitamin B12);
    • about 150 to about 250 mg ascorbic acid (vitamin C);
    • about 30 to about 50 mg nicotinamide (vitamin B3);
    • about 4.5 to about 7.5 mg thiamine (vitamin B1);
    • about 0.1 to about 0.3 mg pyridoxine HCl (vitamin B6);
    • about 2.7 to about 4.5 mg riboflavin 5-phosphate sodium (vitamin B2);
    • about 7.5 to about 15 mg pantothenic acid (vitamin B5);
    • about 0.08 to about 0.125 mg Zinc sulfate heptahydrate; and
    • about 1 ml q.s., sterile water for injection

The aqueous solution is formulated in physiological saline and adjusted an acceptable pH in the range of about 6.5 to about 7.5 to 7.4, thereby minimizing any injecting pain beyond the needle prick. The aqueous solution may be optionally supplemented with a preservative (e.g., from about 0.01% to about 2% benzyl alcohol), a chemical stabilizer (e.g., from about 0.01% to about 2% gentisic acid), and/or an additional bioactive agent (e.g., from about 0.01% to about 2% hyaluronic acid) depending on anticipated delivery method, shelf-life, and intended effects.

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Patent 2024
5'-O-(6-O-malonylglucopyranosyl)pyridoxine Ascorbic Acid Benzyl Alcohol Cobalamins gentisic acid Hyaluronic acid Needles Niacin Niacinamide Obstetric Delivery Pain Pantothenic Acid Pharmaceutical Preservatives physiology Riboflavin Saline Solution Sodium Riboflavin Phosphate Sterility, Reproductive Thiamine Vitamin B6 Vitamins Zinc Sulfate, Heptahydrate
Not available on PMC !

Example 23

In many cases of sexual assault, traces of semen are left behind in the vagina, allowing for later collection and analysis. Semen consists of a variety of proteins, vitamins, nutrients, blood group antigens, and DNA. The preservation and/or analysis of semen can facilitate later development of a DNA profile. In some embodiments, the disclosed kit allows for at-home detection of analytes from semen.

Devices, systems and methods of the present disclosure can be combined with or modified by other devices, systems and methods, such as, for example, those described in International Patent Publication No. WO/2016/025332, which is entirely incorporated herein by reference.

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Patent 2024
Biologic Preservation Blood Group Antigens Medical Devices Nutrients Plant Embryos Semen Analysis Sexual Assault Staphylococcal Protein A Vagina Vitamins

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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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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.

More about "Vitamins"

Vitamins are a diverse group of essential organic compounds that play a vital role in maintaining human and animal health.
These micronutrients cannot be synthesized by the body in sufficient amounts, so they must be obtained from the diet.
Vitamins are required in small quantities for a variety of metabolic processes, and they have crucial functions in preventing disease and promoting overall wellbeing.
The two main types of vitamins are fat-soluble (A, D, E, K) and water-soluble (B-complex, C).
Fat-soluble vitamins are stored in the body's fatty tissues and liver, while water-soluble vitamins are more readily excreted.
Deficiencies in specific vitamins can lead to a range of clinical disorders, underscoring the importance of proper vitamin intake.
Vitamin research is crucial for understanding the effects of these compounds on human health and developing optimal supplementation strategies.
Researchers can utilize tools like PubCompare.ai to enhance the reproducibility of their vitamin studies.
This AI-driven platform helps scientists locate protocols from literature, preprints, and patents, and use AI-comparisons to identify the best protocols and products for their vitamin research, ultimately improving their research outcomes.
In addition to vitamins, other important nutrients for cell culture and research include penicillin/streptomycin (antibiotics), L-glutamine (an amino acid), MEM vitamin solution, sodium pyruvate, MEM vitamins, penicillin, DMEM, non-essential amino acids, and streptomycin.
These components play crucial roles in maintaining cell health, supporting growth, and preventing contamination in various experimental settings.