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Formaldehyde Gel 10%

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YOUR SAFEST CHOICE FOR SURGICAL SPECIMEN PRESERVATION FORMALDEHYDE GEL 10%-SAFER FOR THE ENVIRONMENT AND LAB TECHNICIANS A unique formula designed for storing surgical specimens. It contains a 10% formaldehyde gel solution, which is safer and less harmful to both the environment and laboratory personnel compared to traditional liquid formaldehyde solutions. In pathology laboratories, 10% formaldehyde solutions are commonly used for preserving surgical specimens and biological tissues for diagnostic purposes. However, these solutions release harmful formaldehyde vapors that can irritate the eyes and respiratory system, cause headaches, nausea, and drowsiness. Formaldehyde vapors are also classified as carcinogens by the World Health Organization (WHO). To mitigate these risks, we introduce a novel approach: formaldehyde in a gel form. This innovative formulation retains all the excellent tissuepreserving properties of formaldehyde while significantly reducing vapor levels and strong odors. This contributes to the safety of both laboratory personnel and the environment. INTRODUCING FORMALDEHYDE GEL 10Formaldehyde Gel 10% ENG PDF Formaldehyde Gel 10% ENG PDF% - 1 lt.(Ref.No.: 70154-1000) - 5 lt.(Ref.No.:70154-5000) WHY CHOOSE FORMALDEHYDE GEL 10%? - Superior Tissue Preservation: Formaldehyde Gel 10% offers the same exceptional tissue preservation properties as traditional formaldehyde solutions. - Reduced Health Risks: Say goodbye to harmful formaldehyde vapors. Our gel formulation minimizes irritations, headaches, nausea, and drowsiness associated with traditional formaldehyde. - Environmental Responsibility: We're committed to sustainability. Formaldehyde Gel 10% is safer for the environment and complies with eco-friendly standards. - Easy to Use: Ready-to-use formulation, convenient for laboratory procedures. - Customizable Volume: Our containers come in various sizesand refill options, allowing precise volume adjustments as needed. PROTECT YOUR TEAM, PROTECT THE ENVIRONMENT Enhanced Safety Features: - Gel Consistency: Our gel formulation ensures proper specimen protection, minimizing spillage and leakage risks - Low Vapor Levels: Dramatically reduce formaldehyde vapor exposure, making the laboratory environment safer for technicians. - Odor Control: Say goodbye to strong formaldehyde odors; experience a more pleasant work environment. - pH Balanced: Formaldehyde Gel 10% maintains a neutral pH of 7 for optimal tissue preservation This product is intended for laboratory use only. Please follow all safety protocols and guidelines. MenidiMedica Biotech Greece is committed to environmental responsibility and product safety. Copyright © 2023 MenidiMedica Biotech Greece. All rights reserved.

KaryoPrep General Preservative

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KaryoPrep General Preservative is designed for use with a variety of methods, including: the manual method introduced by MenidiMedica, MenidiMedica LBC system, other commercial processors. During the processing of various biological samples, the user can refill the vial of KaryoPrep Solution for Fixation with the same amount of volume collected for diagnosis. In this way, optimal preservation of the uncollected biological specimen is obtained. It is provided in various volumes in HDPE plastic material. The HDPE material, certified by the provider, is free of BPA, phthalates and latex and does not contain, or contains less than the 0.1% of substances that can be defined as ''high concern'', identified as SVHC and listed in the candidates list in the XIV REACH annex. LBC LEAFLET

IRON CROMAZUROL Colorimetric method Endpoint

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PRINCIPLE The method is based on the properties of Chromazurol S (CAS), a chromogenic iron-binding dye, that under acidic conditions in presence of cetrimide (CTAB) forms an intense purple complex proportional to the concentration of iron present in the sample. REAGENT COMPOSITION R Chromazurol reagent. Acetate buffer, chromazurol, cetrimide, Mg2+, thiourea, Tween 20. C R:35/10 S :26-37/39-45 STORAGE AND STABILITY Store at 2-8ºC. All the kit compounds are stable until the expiry date stated on the label. Do not use reagents over the expiration date. Store the vials tightly closed, protected from light and prevented contaminations during the use. Discard if appear signs of deterioration: - Presence of particles and turbidity. - - Blank absorbance (A) at 635 nm > 0.575 in 1cm cuvette REAGENT PREPARATION The Reagent is ready-to-use. SAMPLES Serum or heparinized plasma. Centrifuge specimen as soon as possible after collection. Hemolyzed samples are rejected. Ruptured red cells falsely elevate the serum results. Iron in serum is stable for 3 weeks at 2-8ºC and for about 7 days at 20-25ºC. Freeze for longer storage. INTERFERENCES - Lipemia (intralipid >1.25 g/L) may affect the results. - Bilirubin (< 10 mg/dL) does not interfere. - Hemoglobin may affect the results. - Other drugs and substances may interfere MATERIALS REQUIRED - Photometer or colorimeter capable of measuring at 635 ± 20 nm. - Pipettes with disposable plastic tips to measure reagents and samples. - Disposable plastic tubes for the tests. PROCEDURE 1. Bring reagents and samples to room temperature. 2. Pipette into labelled test tubes: (For cal.) R: 1000 uL. + cal.: 50 uL. (For sample) R: 1000 uL. + sample: 50 uL. 3. Mix and let the tubes stand 10 minutes at 37ºC. 4. Read the absorbance (A) of the samples and the standard at 635 nm against the reagent blank. CALCULATIONS A Sample/A Standard x C Standard = ug/dL iron Samples with concentrations higher than 1000 ug/dL should be diluted 1:2 with saline and assayed again. Multiply the results by 2. If results are to be expressed as SI units apply: ug/dL x 0.179 = umol/L. REFERENCE VALUES Men = 60 - 175 ug/dL (10.7 - 31.3 umol/L) Women = 50 - 170 ug/dL (9.0 - 30.4 umol/L) Note: It is recommended that each laboratory establishes its own reference range QUALITY CONTROL The use of a standard to calculate results allows to obtain an accuracy independent of the system or instrument used. To ensure adequate quality control (QC), each run should include a set of controls (normal and abnormal) with assayed values handled as unknowns. If the values are found outside of the defined range, check the instrument, reagents and procedure. Each laboratory should establish its own Quality Control scheme and corrective actions if controls do not meet the acceptable tolerances. CLINICAL SIGNIFICANCE Following intestinal absoption of iron or erythrocyte destruction, iron ions are released into the plasma where they bind to either apotransferrin or apoferritin proteins to form transferrin and ferritin, respectively. The former helps transport iron to bone marrow for erythropoiesis; the latter stores iron in tissues, until is needed. An increase in the iron level in plasma due to rapid destruction of erythrocytes or excesive uptake of iron may also lead to iron overload. The latter causes iron deposition disorders in tissue known as hemosiderosis or hemochromatosis. Conversely, a decrease in the iron level in plasma due to malnutrition or malabsorbtion may lead to excesive depletion in iron storage, resulting in anemia such as iron-deficiency anemia. NOTES - Contamination of glassware with iron will affect the test. Use acid-washed glassware or plastic tubes. - This method may be used with different instruments. Any application to an instrument should be validated to demonstrate that results meet the performance characteristics of the method. It is recommended to validate periodically the instrument. Contact to the distributor for any question on the application method. - - Clinical diagnosis should not be made on findings of a single test result, but should integrate both clinical and laboratory data. ANALYTICAL PERFORMANCE Detection Limit: 10.10 ug/dL Linearity: Up to 1000 ug/dL Precision (expressed in ug/dL): Within-run Mean - 118.8, 204.6 SD - 0.95, 0.59 CV% - 0.81, 0.59 N - 10, 10 Between-run Mean - 118.8, 204.6 SD - 2.71, 3.71 CV% - 2.28, 1.81 N - 10, 10 Sensitivity : 1.6 mAbs / ug/dL iron. Correlation: This assay (y) was compared with a similar commercial method (x). The results were: N = 49 r = 0. 97 y = 0.97x + 0.10 The analytical performances have been generated using on automatic instrument. Results may vary depending on the instrument. IRON CROMAZUROL PDF

Sperm DNA Fragmentation Kit

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SPERM DNA FRAGMENTATION KIT UNLOCK THE FUTURE OF PARENTHOOD WITH SPERM DNA FRAGMENTATION KIT What is Sperm DNA Fragmentation Kit? The Sperm DNA Fragmentation technique can distinguish between functional and non-functional spermatozoa based on their DNA integrity, identifying which ones are viable for fertilization. This kit evolutionizes the assessment of sperm quality by complementing traditional sperm analysis. While conventional semen analysis focuses solely on sperm concentration, motility, and morphology, it overlooks a crucial parameter: the integrity of the DNA molecule. Interestingly, 15% of men classified as infertile have normal sperm analyses, underscoring the need for a more comprehensive evaluation. Sperm DNA fragmentation kit empowers medical professionals to make informed decisions about the most suitable assisted reproduction techniques for each couple. Employs a controlled DNA denaturation process to facilitate the removal of proteins from each spermatozoon. This method results in the formation of halos composed of DNA loops at the head of healthy sperm, a feature absent in sperm with damaged DNA. Key Features of Sperm DNA Fragmentation Kit - Easy & Quick Assessment: Say goodbye to complex laboratory equipment. Our kit provides a hassle-free, rapid measurement of Sperm DNA Fragmentation. - Comprehensive Insights: Complement traditional semen analysis with specific data on genetic material quality for a holistic evaluation. - Cost-Effective: Avoid expensive and frustrating IVF procedures. Assess Sperm DNA Fragmentation beforehand to guide fertility treatment. - Vital for Success: The integrity of paternal DNA is critical for both natural conception and assisted reproduction, ensuring the best chance of a viable pregnancy Who can use Sperm DNA Fragmentation Kit? Medical professionals rely on information provided by MenidiMedica Biotech solutions as an essential addition to the standard semen analysis when initiating treatment. Sperm DNA damage is a complex process influenced by various factors. Therefore, it is particularly recommended for the following groups: 1. Couples who have experienced recurrent miscarriages. 2. Couples facing unexplained infertility lasting more than six months. 3. Men aged over 40. 4. Individuals who frequently wear tight-fitting clothing. 5. Men with a history of cancer. 6. Men undergoing treatment with prescription medications. 7. Men exposed to harmful substances or toxins. 8. Men who have had urogenital infections. 9. Individuals with unhealthy lifestyle habits, including smoking, physical inactivity, poor dietary choices, or obesity. 10. Cases where the quality of embryos during subsequent cycles of egg donation is suboptimal. 11. Unexplained male infertility. Natural factors such as improper maturation and oxidative stress can lead to disruptions in spermatozoa production within the testicles, resulting in fertility challenges. Why Choose Sperm DNA Fragmentation Kit? - Accurate Evaluation: Obtain precise results with high-contrast halo images using standard bright-field microscopy after Wright staining. - Sperm Identification: Preserve sperm tails for easy differentiation from other cell types and identification of degraded sperm cells with varying halo sizes. - User-Friendly: A simple protocol involving acid treatment and lysis solution makes it easy to assess DNA integrity. - Functional vs. Non-Functional: Identify which spermatozoa are functional for fertilization and distinguish them from non-functional ones. How Does It Work? Our cutting-edge technique is based on the principle that sperm with fragmented DNA do not display the characteristic halo of dispersed DNA loops found in sperm with intact DNA after acid denaturation and nuclear protein removal. Fresh semen samples should be collected in a sterile recipient. The sperm DNA fragmentation assay should be performed immediately once the sperm sample has been obtained or thawed after cryopreservation. a. The spermatozoa are placed in an agarose microgel and evenly distributed onto a slide. b. The sample is subjected to acid denaturation and a lysis solution as part of the treatment process. c. After treatment, the sample undergoes dehydration, staining, and subsequent microscopic visualization for examination of fragmented and non-fragmented DNA. d. To calculate the percentage of sperm with fragmented DNA (SDF), count SDF sperm based on specified criteria and divide by the total sperm counted (N), then evaluate the SDF percentage in relation to established thresholds for SDF levels. Storage Conditions Upon receipt, please store the kit in a location with a temperature range between 2ºC and 30ºC, and ensure it is shielded from exposure to light. Once the kit is opened, it maintains stability for a period of 12 months. Description of kit reagents Every kit contains the necessary to perform 10 assays. The components are: - Agarose Tubes; 10 units - Denaturant Agent 1 mL screw tube - Lysis Solution, six 20 ml bottle each Sperm classification In each sample, a minimum of 300 spermatozoa should be counted, following the specified criteria for categorization: Spermatozoa without DNA fragmentation: - Spermatozoa with big halo: Sperm with halos whose width is equal to or greater than the diameter of the core (referred to as "Big halo"). - Spermatozoa with medium-sized halo: Sperm with halos sized between those with large halos and those with very small halos (referred to as "Medium halo"). - Others: Cells referred to as "others" that do not correspond to spermatozoa, distinguished by the absence of a tail. These cells must not be included in the estimation of the frequency of sperm with fragmented DNA. Spermatozoa with fragmented DNA: - Spermatozoa with small halo: Sperm displaying halos with a width equal to or smaller than 1/3 of the diameter of the core (referred to as "Small halo"). - Spermatozoa without halo: Sperm with no visible halo (referred to as "Without halo"). - Spermatozoa without halo and degraded: Sperm that lack a halo and exhibit irregular or weak staining of the core (referred to as "Degraded"). Order Your Sperm DNA Fragmentation Kit Today! Make the right choices on the path to parenthood. The Sperm DNA Fragmentation Kit empowers medical professionals with the knowledge needed for fertility journey. Contact us now to order your kit. We strive for a better, safer world for us and our children. SDF-ENG-PDF

KaryoPrep CellWhole Reagent

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KaryoPrep CellWhole Reagent is designed and developed for urine biological samples which have few cells for examination. One drop from KaryoPrep Cell Whole Reagent on a glass slide is enough for stamping and processing of this kind of samples. It is provided in various volumes in HDPE plastic material. The HDPE material, certified by the provider, is free of BPA, phthalates and latex and does not contain, or contains less than the 0.1% of substances that can be defined as ''high concern'', identified as SVHC and listed in the candidates list in the XIV REACH annex. LBC LEAFLET

Bromate Direct

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QUANTITATIVE DETECTION OF BROMATE IN BREAD Potassium bromate, or simply called bromate, is an oxidiser used to strengthen dough and enhance its elasticity. This helps bake uniform and whitened bread. However, excessive use of potassium bromate results in residual concentrations in bread having potentially harmful effects. Some people who ingested large amounts of bromate had gastrointestinal symptoms such as nausea, vomiting, diarrhea and abdominal pain. Some individuals who ingested high concentrations of bromate also experienced kidney effects, nervous system effects and hearing loss. European bread lacks a specific ingredient: Potassium bromate. Food makers in the United States regularly use this chemical compound to strengthen dough. In fact, this additive is present in more than 100 products. But, Europe, China, and India have banned Potassium bromate due to concerns that it may be a carcinogen. CHARACTERISTICS Reference: 82906 Linearity range: 0.5 - 50 ug/mL. bromate content Presentation: Chromogen Activator R1 - 5 mL., Substrate R2 - 2 mL. Sample Matrices: bread, water Expiry Date: 24 months *The kit must be stored at 2°-8°C HOW TO USE Method: Quantitative, Endpoint Wavelength: 505 nm Sample preparation: Collect 1 gr. of bread, cut and mix in 20 mL. distilled water with magnetic stirrer. Filter through Whatman 41 filter. Blank: Reagent Procedure: 1. Read Blank 2. Transfer 880 uL. sample filtrate into a cuvette 3. Add 100 uL. R1 and mix 4. Add 20 uL. R2, shake in vortex for 1' 5. Read results The color is stable for 30' BROMATE DIRECT ENG PDF

TETHYS: UNIQUE RAPID CARIES DETECTION TEST

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THE FUTURE OF ORAL HEALTH: UNIQUE RAPID CARIES DETECTION TEST JOIN THE ‘BETTER ORAL HEALTH MOVEMENT FOR ALL’ The majority of participants in our clinical trial (90%) recognised the importance of early detection of caries. Boost your oral health and enjoy a healthier smile. TAKE CHARGE OF YOUR ORAL HEALTH Globally, in 2019, 3.09 billion new cases of caries in permanent teeth were recorded (an increase of 48.00%), as well as 2.03 billion existing cases of caries (an increase of 46.07%), compared to 1990. Among adolescents aged 12 to 19 years, more than half (57%) had at least some dental decay from caries in their permanent teeth. In adults aged 20 years and older, 90% had at least one dental decay from dental caries. EARLY DETECTION FOR A HEALTHIER SMILE Tooth decay is a silent threat to your oral health, but with our revolutionary TETHYS rapid caries detection test, you can now detect it early and take control of your dental wellbeing. WHY CHOOSE THE RAPID CARIES DETECTION TEST? Product of cooperation between MenidiMedica Biotech Greece and the University of West Attica. TETHYS diagnostic test for valid, early detection of dental caries, ensuring oral hygiene. - Fast and reliable: you get results within minutes, allowing early detection of caries even in its early stages. - Accurate: Our test has high sensitivity and specificity, ensuring accurate detection of caries. - Convenient: No invasive procedures or specialized equipment are required. A simple swab and a vial is all that is needed. - Safe: The test is safe and non-invasive, making it suitable for all ages. - Proven results: Backed by clinical trials, our test has shown excellent performance. HOW IT WORKS? - Open the sterile wooden swab. - Brush your teeth as usual. - Open the vial of single reagent and rinse the head of the swab in the vial. - Break off the wooden swab head and place it in the vial - Close the vial and shake gently for 5 seconds. - Place the vial in your pocket for 30 minutes. - Check for a colour change in the reagent: a. Magenta for a positive result. Have caries in progress b. Pink or transparent clear for a positive result. You have caries and a decaying tooth c. Purple for a negative result. You do not have caries DETECT-PREVENT-RESIST Don't let tooth decay develop into a painful problem. With the TETHYS quick caries test, you take control of your oral health in your own hands. CLINICAL TRIAL RESULTS - Sensitivity: 98,39% - Specificity: 100.00% - Positive predictive value (PPV): 100.00% - Negative predictive value (NPV): 99.19% - Accuracy: 99.46% tethys eng pdf

Lugol Solution 5%

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Content Iodine, Preservatives, Buffer Description Lugol Solution How Supplied Glass bottles of 100, 200, 500, 1000 mL. Action & Uses LUGOL Solution 5% is an agent used for differentiating normal from suspicious tissues. Normal tissue stains brown due to its high glycogen content, while tissue suspicious for malformations does not stain, and thus appears pale compared to the surrounding tissue. Wash after use with water or normal saline. Warnings For External Use Only. Should inadvertent ocular administration occur, the eye(s) should be washed immediately with large amounts of water or normal saline, occasionally lifting the upper and lower lids until no evidence of solution remains (approximately 15-20 minutes). Storage Keep tightly closed and protect from light. DO NOT use if seal is broken. Store at room temperature 15°- 30°C. Disposal Opened containers with unused portions of product should be placed in a suitable, dry container for later disposal according to local hazardous waste practices. Lugol Solution 5% IFU ENG PDF

Fast Bromate

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QUALITATIVE DETECTION OF BROMATE IN BREAD Potassium bromate, or simply called bromate, is an oxidiser used to strengthen dough and enhance its elasticity. This helps bake uniform and whitened bread. However, excessive use of potassium bromate results in residual concentrations in bread having potentially harmful effects. Some people who ingested large amounts of bromate had gastrointestinal symptoms such as nausea, vomiting, diarrhea and abdominal pain. Some individuals who ingested high concentrations of bromate also experienced kidney effects, nervous system effects and hearing loss. European bread lacks a specific ingredient: Potassium bromate. Food makers in the United States regularly use this chemical compound to strengthen dough. In fact, this additive is present in more than 100 products. But, Europe, China, and India have banned Potassium bromate due to concerns that it may be a carcinogen. CHARACTERISTICS Reference: 82906A Linearity range: 0.5 - 50 ug/mL. bromate content Presentation: Chromogen Activator R1 - 10 mL., Substrate R2 - 3 mL. Sample Matrices: bread, water Expiry Date: 24 months *The kit must be stored at 2°-8°C HOW TO USE 1. Add 4 drops of R1 or 200 uL. of R1 to 1 gr. bread 2. Add 1 drop of R2 or 60 uL. of R2 to 1 gr. bread INTERPRETATION Yellow: Absence of bromate additive in bread Red: Presence of bromate additive in bread FAST BROMATE ENG PDF

VagoClean

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Your Solution for Persistent Bacterial Vaginal Infections. - Reagent in 10 mL. Single Dose in packages of 5x10 mL. and 10x10 mL. - Ref. Number: 70996-5, 70996-10 “Experience Relief and Well-Being” What is a Bacterial Vaginal Infection? Bacterial vaginal infections are common health issues affecting women of all ages. They occur when the delicate balance of bacteria in the vaginal area is disrupted,leading to discomfort and unpleasant symptoms. Such infections are typically caused by an overgrowth of harmful bacteria, and they can result in: - Itching and Irritation - Abnormal Vaginal Discharge - Burning Sensation - Unpleasant Odor If left untreated, bacterial vaginal infections can lead to more serious complications, including: - Pelvic Inflammatory Disease (PID) - Recurrent Infections - Premature Birth (in pregnant women) “Introducing VagoClean - Your Solution!” Easy-to-Use Kit VagoClean, a product of MenidiMedica Biotech Greece, is here to help you take control of your vaginal health. Our 10 mL single-dose reagent offers a convenient and effective solution for cases where traditional therapeutic treatments have not yielded the desired results. How It Works 1. Immerse the content of the monoreagent in sterile gauze provided. 2. Gently insert the sterile gauze into the vagina for local washing. 3. Leave it in for 1 minute. 4. Remove the sterile gauze. If symptoms of bacterial infection persist, repeat the medical procedure after 8 calendar days with VagoClean for comprehensive relief. Benefits of VagoClean - Fast and Effective Relief - Maintains Vaginal Balance - Easy-to-Use Kit - Sterile and Safe - Supports Your Well-Being VagoClean is intended for use by gynecologists only. It is a specialized product designed to address bacterial vaginal infections in a clinical setting under the guidance of healthcare professionals. Please consult with your gynecologist for proper usage and treatment. VagoClean Commercial Leaflet ENG pdf

Proteins in Milk & Cheese

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QUANTITATIVE DETECTION OF TOTAL PROTEINS IN MILK & CHEESE Proteins are chains of amino acid molecules connected by peptide bonds. Milk proteins contain all 9 essential amino acids required by humans. Milk proteins are synthesized in the mammary gland, but 60% of the amino acids used to build the proteins are obtained from the cow's diet. Total milk protein content and amino acid composition varies with cow breed and individual animal genetics. Following a comparative analysis of MenidiMedica's Biotech Greece Proteins in Milk & Cheese method and the Kjeldahl reference method, it is evident that the former is the most appropriate choice. This is due to its ability to deliver rapid and precise results in contrast to the Kjeldahl method. Additionally, the Biotech Greece assay offers a straightforward protocol, eliminating the need for costly equipment or skilled analysts to gather the data. BENEFITS - RAPID - Results in 60 seconds - SENSITIVE/Adapted to specific regulation - RELIABLE AND ROBUST - USER FRIENDLY/Easily performed in lab - COST EFFECTIVE HOW TO USE Method: Quantitative, Point-Point Wavelength: 578 nm Sample preparation 100 uL. raw milk + 900 uL. distilled water and mix Blank: Distilled water Procedure: 1. Read Blank 2. Add 300 uL. reagent R to a cuvette 3. Add 10 uL. sample matrix to the cuvette 4. Incubate 60 seconds 5. Read results CHARACTERISTICS Reference: 83010 Limit of Detection (LoD in%): 0.1 g/dL. of total proteins in milk and cheese Presentation: Vial of 15 mL. reagent R Sample Matrices: Raw milk (e.g. cow, goat, sheep, buffalo, camel) Expiry Date: 24 months *The kit can be stored at room temperature for 6 months or at 2°-8°C for 24 months PROTEINS IN MILK AND CHEESE ENG PDF

Fast Formaldehyde

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Formaldehyde Adulteration in fish, food, meat, milk, water Description Formaldehyde is the simplest aldehyde. It is widely employed in industry (meat, fruits, fish, water) for wide range of applications, as a disinfectant and is a commonly utilized tissue fixative and embalming agent. Formaldehyde is naturally present in all tissues and body fluids. Recently, it has been shown that some cancer types exhibit elevated formaldehyde levels. Examples of foods known to contain naturally occuring formaldehyde. Food Type/ Level (ppm-mg/kg) Apple: 6.3-22.3 Banana: 16.3 Cauliflower: 26.9 Pear: 38.7-60.0 Mushroom (dried/raw): 100-406/6-54.4 Beef, pork, mutton and poultry meat: 2.5-20 Cod: 4.6-34 Fish ball: 6.8 Crustacean: 1-98 Key features Fast Formaldehyde detection is an ideal kit for the presence of added formaldehyde in food (milk, fish, etc.). The only part that changes in the procedure is the preparation of the sample Validated - High precise correlation with AOCS Official Method 897.01 Applications - Formaldehyde presence in biological samples, food, water, fish, meat, fruits Kit contents R - 2 x 12.5 mL. Note: Use R with caution, wearing protective gloves. Necessary equipment (not provided) Pipette variable volume 100-1000 uL Water bath, peltier plate or incubator Sample preparation and procedure for milk 1. Add 500 uL. of raw milk in a test tube 2. Add 500 uL. of reagent R in the test tube 3. Mix for 5 seconds 4. Incubate the content in a water bath or peltier plate for 3-5 minutes at 50°C 5. Read the formed colors Sample preparation and procedure for fish 1. Cut 1 cm3 of raw fish and mince it and place it in a tube 2. Add 5 mL. of distilled water in the tube 3. Mix the suspension 4. Collect 500 uL. of suspension in a test tube 5. Add 500 uL. of reagent R in the test tube 6. Incubate the content in a water bath or peltier plate for 3-5 minutes at 50°C 7. Read the formed colors *Note: For other food sample preparations, contact MenidiMedica Biotech Greece Interpretation (for milk) - Fade pink = Pure food with no added formaldehyde - Yellow = Adulterated food with formaldehyde (0.025%) - Green = Adulterated food with formaldehyde (9%) MSDS is available upon request. Fast Formaldehyde IFU ENG PDF

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