BIOL 1F90 Expt. #1: Protein Quantification Student Name: Carlos Osorio Student ID: 5220710 Lab Section: 34 Date Experiment Performed: Sept. 26th‚ 2012 Lab Partners: K. Cloutier J. Yang ABSTRACT Protein concentration analysis is primarily done through an accepted form commonly referred to as the Bradford Protein Assay. The main purpose of this experiment was to observe and record the various protein samples’ absorbency values through the calibrated readings of a spectrophotometer
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Full Report on Exercise 4.2 ESTIMATION OF PROTEIN CONCENTRATION BY SPECTROPHOTOMETRY And Exercise 4.3 GEL FILTRATION CHROMATOGRAPHY Joel Don M. Untalan CHEM 160.1 – 1L AY 2013 – 2014 Groupmates: Sonette Yao Kristopher Quilan Laboratory Instructor Carmelo C. Briones I. Introduction Analyzing proteins in determination of protein concentration by spectrophotometry is important. It determines to what concentration of a certain protein is in a crude sample. In this technique‚ a wide
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Experiment 2 Quantification of Proteins in Solution by Spectrophotometer Lab bench# 1 Introduction: Absorption spectroscopy is a common method for finding the concentration of proteins or protein complexes in a solution. Proteins absorb light at specific wavelengths and can be defined by the equation A = log (Io/I). This equation states that an absorbance at a specific wavelength‚ A is equal to the log of the ratio of incident light intensity (Io)‚ to transmitted light intensity (I). A
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We successfully adapted a commercially available protein detection assay for the quantiWcation of PEI. All experiments described below were performed with linear 25-kDa PEI (Polysciences‚ Warrington‚ PA‚ USA) that we routinely use for the transfection of mammalian cells [4]‚ but it was possible to quantitate other PEIs (diVerent molecular weights; branched) with this method (data not shown). The mixing of a PEI solution with the Advanced Protein Assay (APA) reagent (Cytoskeleton‚ Denver‚ CO‚ USA)
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Estimation of protein concentration Introduction Protein assays are designed to measure the total protein in a solution. Protein assays are quantitative if the protein to be assayed is available in sufficient quantity such that one is able to use it to create a standard curve. If this cannot be achieved‚ then a standard protein‚ such as albumin‚ may be used for a standard curve with the understanding that the results on the unknown protein are semi-quantitative. Since most proteins are not available
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QUANTITATIVE DETERMINATION OF COPPER (II) CONCENTRATION BY SPECTROPHOTOMETRY D.DEL PRADO1‚ J. BELANO1‚ M.MAHUSAY2‚and M.FRANCISCO2 1 DEPARTMENT OF FOOD SCIENCE AND NUTRITION‚ COLLEGE OF HOME ECONOMICS 2INSTITUTE OF CHEMISTRY‚ COLLEGE OF SCIENCE UNIVERSITY OF THE PHLIPPINES‚ DILIMAN‚ QUEZON CITY 1101‚ PHILIPPINES DATE SUBMITTED: 12 MARCH 2013 DATE PERFORMED: 7 MARCH 2013 ------------------------------------------------- ------------------------------------------------- ABSTRACT -------------------------------------------------
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interaction of electromagnetic radiation with chemical compounds (Stewart & Ebel‚ 2000). By using spectrophotometric analysis or spectrophotometry‚ one can determine the identity in terms of structure and species of a biomolecule as well as establish the concentration of a certain biomolecule (Stewart & Ebel‚ 2000). Absorption spectrophotometry is the most common of spectrophotometry technique used by biochemist. The science behind this technique is when light passes through a solution‚ components or substances
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SPECTROPHOTOMETRY Herman‚ Harmon Chris T. 1Prof. Meynard Austria‚ of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology‚ Chm171L/A1‚ School of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology‚ Experiment # 4 [pic] ABSTRACT The objectives of this experiment are to examine the components of a simple spectrophotometer- the Jenway 6100 & Perkin Elmer Lambda 40. As well as to determine the absorption spectrum of a solution
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Chapter 2 Basis of Derivative Spectrophotometry 2.1 The Main Law of Light Absorption by a Substance Photobiological processes occur under the influence of light of ultraviolet (UV)‚ visible‚ and near infrared spectral regions. Generally‚ values of light flux intensity‚ I‚ and wavelength‚ l are used in optical measurements. The frequency index n is also considered to characterize an absorbed light. Frequency is expressed in reciprocal seconds [cÀ1] and presents itself as the ratio
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determining the different concentrations of potassium permanganate solutions by finding its absorbance through the use of spectrophotometer. Four known concentrations were prepared; 2.5 x 〖10〗^(-3) M‚ 6.25 x 〖10〗^(-4) M‚ 1.25 x 〖10〗^(-4) M‚ 6.25 x 〖10〗^(-4) M. The solutions were placed on the spectrophotometer to determine absorbance together with the unknown. Distilled water was placed before each trial to ensure the accuracy of results. Determining the concentration of the unknown sample was
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