Table 5.4: Floating Behavior of In-Situ Gel formulation of etodolac S. NO. Formulation code Floating lag time (sec) floating time (hr) 1 P1 26 >12 2 P2 35 >12 3 P3 50 >12 4 P4 66 >12 5 P5 196 >12 6 P6 219 >12 7 P7 45 >12 8 P8 72 >12 Table 5.5: Gelling capacity of In-Situ Gel formulation of etodolac S.NO
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terms (excluding inflation) sales will slip very slightly. Q: Which segments have most potential for growth? A: There is a clear divide between two promising segments – liquid soaps and shower gels – and two less buoyant ones – bar soaps and bath additives. Mintel expects liquid soap and shower gel
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LISMA RUHILA BT ALIAS Group: AS201 5A Experiment: GEL ELECTROPHORESIS OF EXTRACTED DNA 0.5% AGAROSE GEL Group partners: 1) HALIMATUN SAADIAH BT MOHD BUSTAMAM 2) NUR FARHANA BT AHMAD SOPIAN 3) FATIN NUR ASYIQIN BT ABD TALIB 4) UMMU AFIQAH BT HASSAN 5) NABIHAH BT MD NAWAWI Date of experiment: 8th October 2012 Date of submission: 15th October 2012 TITLE: GEL ELECTROPHORESIS OF EXTRACTED DNA 0.5% AGAROSE GEL DATE: 8th OCTOBER 2012 OBJECTIVE * To study measure
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Scenario 1 Energy Inc. has a present obligation (IAS 37-17) and probable liability (ASC 450-20-25-2) on December 31‚ 2011 as a result of a past event‚ the contamination of the land‚ because it is virtually certain that a draft law requiring cleaning up will be enacted. It is probable (more likely than not) that Energy Inc. will be required to transfer economic benefits in settlement which is an outflow of resources embodying economic benefits in settlement (IAS 37-23). The amount of the obligation
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other materials may be stored at room temperature (approximately 25°C). Use and Lab Safety: The materials supplied are for use with the method described in this kit only. Use of this kit presumes and requires prior knowledge of basic methods of gel electrophoresis and staining of DNA. Individuals should use this kit only in accordance with prudent laboratory safety precautions and under the supervision of a person familiar with such precautions. Use of this kit by unsupervised or improperly
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Q3 - OverallImpression Based on your overall impression of Southwestern Energy and using a six-point scale where 6=a very positive impression and 1=a very negative impression‚ please tell me how you would rate the company. "3 [6-pt scale]. If it’s an absolute scale as an investment opportunity and I don’t think you should own any energy stocks‚ they are an energy stock. Again‚ that’s why I asked if it was a relative scale or not. On a relative scale‚ 3." Q4 - OE_Strengths What do you see as Southwestern
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Julie Conlon Ambit Energy December 18‚ 2011 Julie.Conlon@carestreamhealth.com 585.709-8948 The Federal Energy Agency started energy deregulation in the late 1980’s and early 1990’s‚ mostly because many local energy companies such as New York’s RG&E‚ had formed monopolies‚ they also felt that these companies were using outdated‚ inefficient generating plants. Consumers had no choice‚ and were forced to pay escalated energy costs based on solo area providers. It has
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for Bangladeshi consumers‚ which are best suited to their needs On the other hand Meril baby gel toothpaste is made for baby with a special formulation that ensures gentle care of your baby’s milk teeth and gums. Baby’s teeth and gums are so soft and delicate that an adult tooth paste can do more harm than doing well. On this repot we compare Strength and Weakness for pepsodent toothpaste and meril baby gel toothpaste. We do Segmentation‚ Target Market‚ Positioning for those product.then we do Comparative
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Gel Electrophoresis is used to separate the haemoglobin component of blood. Because each type of haemoglobin (HbA‚ HbS‚ Hbc and more) have different electrical charges‚ they will separate after undergoing gel electrophoresis. Firstly‚ a blood sample from the patient is taken and is applied to a cellulose acetate membrane strip that has been soaked in a buffer solution along with saponin. The red blood cells are lysed by the saponin while being soaked‚ therefore they release their haemoglobin. A
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The two techniques that were used to create a DNA profile in this experiment were PCR and gel electrophoresis. The PCR is used to amplify the several DNA samples and gel electrophoresis is performed to separate the DNA fragments according to their size. [6] In the first part of the experiment‚ PCR amplification of the DNA templates was performed and the products obtained were used to perform gel electrophoresis. The process of PCR allows for the amplification of the DNA samples and the components
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