Buffer solution

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    Dna Extraction Lab Report

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    it would seem that if we were to extract DNA without chemicals like lysis solution, concentrated salt solution, resuspenstion buffer, ethanol or isopropyl alcohol, it would result in poor DNA results. Method one Method one to create a perfect result and to extract the optimal DNA, I would believe that we would need centrifuge, sample tube, micropipettors, lysis solution, concentrated salt solution, resuspenstion buffer,…

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    reaction tubes were used to mix reaction buffer, qualified water, Bam HI or Eco RI, and DNA 1, DNA 2, or DNA 3 to reach a final volume of 30 µl. The restriction enzymes were added last to avoid possible errors or inactivation. The each solution were mixed in order to avoid dense layers of enzyme solution at the bottom of the tube. Each tubes were incubated for 60 minutes in a 37oC water bath to guarantee cleavage of DNA. Eventually, 5 µl of 10x gel loading solution was added to each reaction in…

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    The Xmax of the drug was determined by scanning above solution between 400 and 200 nm using UV –visible spectrophotometer. i) In 0.1 N HCL : Drug is calibrated in 0.1 N HCL by using UV spectrophotometer at determined wavelength. ii) In PH 6.8 Phosphate buffer: Drug in calibrated in PH 6.8 Phosphate buffer by using UV-spectrophotometer at determined wavelength. Preparation of mucoadhesivebuccal tablet. Mucoadhesivebuccal…

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    α-Lactalbumin, a multifunction protein in milk, forms an enzyme complex with galactosyltransferase that catalyzes the last reaction in lactose synthesis.1 α-Lactalbumin has one Ca2+ binding site and several Zn2+ binding sites as well as many intermediary folding states, making it ideal for research involving the effects of cation binding on protein interactions as well as research on protein misfolding.1 α-Lactalbumin gives milk an antimicrobial property, making it important for infant health,…

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    chemical constancy in aqueous buffer solution of acidic medium and the comprehensive discharge performance was found in prodrug…

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    Acid-Base Balance

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    CO2 bringing the pH back to normal. The same applies when your pH becomes too high, just reversed. We also have buffer systems that help control our blood pH which help in sudden shifts towards acidity or alkalinity. Two of the important buffer systems include the carbonic acid buffer system where a weak acid is formed from carbon dioxide dissolved in blood and the bicarbonate ion buffer system that corresponds with a weak…

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    a new product. This product is a disk drive. The drive is selling better than expected which causes Foster to worry about the availability of the product and the repercussions if they cannot find a solution to the inventory problem. The product line could potentially become extinct if a solution is not reached, which would affect many stakeholders such as customers, producers and manufacturers of the product, and the salesmen that sell the product. Foster voices his concerns in an email to…

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    Probiotic GOS Essay

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    cotton cloth (approximately 4.5g) in a glass column reactor (whose diameter =9mm) with a water jacket which maintained temperature constant at 40*C. ↓ Take solution of lactose in flask (50ml total volume of solution). ↓ Then continuously re-circulate with the help of immobilized enzyme reactor which work at the flow rate that is 90mL/min.(Albayrak and Yang 2002)…

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    digestion: In this experiment there was a total of 8 tubes prepared with the final volume of 20 μL. Starting with test tube 1, 2, and 4, there was 10μL of water, 10 μL of nucleic acid, and 2 μL of buffer solution (10X) are all added. In test tube 3,5, and 6 there was 5 μL of water, 10μL of nucleic acid, 2μL of buffer and 3 μL of DNase added. Although in test tube 6 the DNase is heated making in inactive. All of the other DNase are active and can consume the DNA present in the test tubes. In test…

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    4.2.3.5. Antioxidant assays in gastric tissue homogenate 4.2.3.5.1. Catalase activity Catalase activity in the gastric tissue was measured according to the procedures of Sinha (1972). One ml of homogenate solution was taken and mixed with 5 ml of phosphate buffer of pH 7.4. To this 4 ml of 0.2 M H2O2 was added and time noted. Exactly after 180 seconds of adding H2O2, a set of 1ml of reaction mixture from the above was taken and 2 ml dichromate acetic acid was added. It was then kept in a boiling…

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