Part CCalculate to three decimal places the charge on a-melanotropin at pH value of 5.Express your answer using three decimal places.VE ΑΣΦSubmit Request AnswerPart DCalculate to three decimal places the charge on a-melanotropin at pH value of 1.Express your answer using three decimal places.VE ΑΣΦSubmit?Request Answer? Properties of some amino acids found in proteinspKa oflonizing SideChain12.5NameArginineAsparticacidCysteineGlutamicacidAbbreviations 1- and3-letterR, ArgD, AspC, CysE, GluHistidineH, HisLysineK, LysTyrosine Y, Tyr3.98.34.26.010.010.1Approximate values found for side chains on thefree amino acids. W.P. Jencks and J. Regenstein(1976) lonization constants of acids and based inHandbook of Biochemistry and Molecular Biology,3rd ed., G. Fasman (ed.), CRC Press, Boca Raton,FL.a-melanotropin (Ser-Tyr -Ser -Met- Glu -His – Phe -Arg –Trp- Gly –Lys— Pro – Val),given.Lillavalues would you expect theAssume the pKas of the N- and C-termini are 7.9 and 3.8, respectively. For side chains, assume the pKą values

Net charge on the amino acid with negative side group: Net charge on the amino acid with positive…

Answered: Part C Calculate to three decimal…

Curren'S Math For Meds: Dosages & Sol

11th Edition

ISBN:9781305143531

Author:CURREN

Publisher:CURREN

Chapter5: Unit, Percentage, Milliequivalent, Ratio, And Household Measures

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Copy and paste the link below and watch the video on Youtube https://www.youtube.com/watch?v=8RBs0Ghg_48 Answer the following Questions: 1. What are the chemicals and materials used in gel electrophoresis? 2. Draw a schematic diagram of a gel electrophoresis set-up 3. Describe the procedure in doing a gel electrophoresis experiment. Why is there a need for a leveling bubble/leveler? What is the use of the rubber dam? 4. What is the use of ethidium bromide and why must you wear gloves when you handle it? 5. What makes the DNA fragment move towards the positive plate? 6. What is the purpose of glycerol in the sample buffer? 7. What is the use of a DNA ladder? 8. What will happen when you increase the voltage of the set-up? 9. Can gel electrophoresis be used to separate amino acids? If so, how is it done?
You have an order for 1 gram of Cefazolin in D5W 100 ml. You have added 5 ml of sterile water to the 1 gram vial to reconstitute powder. However the recommended manufacturer’s diluent amount is 10 ml of sterile water for a final concentration of 100 mg/ml. How would reconstituting the vial with 5 mls affect the concentration and the final calculated dose. Please answer with explanation ASAP. I will really upvote. Thanks
First base U v A G 1.) 2.) 3.) U UUU UUC UUA UUG 1.) 2.) 3.) Phe Leu CUUT CUC CUA CUG GUUT GUC GUA GUG Leu AUU AUC lle AUA AUG start Met or Val Second base C A UCU UCC UCA UCG CCU CCC CCA CCG ACU ACC ACA ACG GCU GCC GCA GCG Ser Pro Thr Ala UAU UGU Tyr Cys UAC UGC UAA Stop UGA Stop A UAG Stop UGG Trp CAU CAC CAA CAG AAU AAC AAA AAG GAU GAC GAA GAG His Gin Asn Lys Asp G Glu CGU CGC CGA CGG AGU AGC AGA AGG GGU GGC GGA GGG Arg Ser Arg Gly UCAG с UCAG А UCAG с А UCAC с G Provide the nine base sequence of the mRNA in triplet form. 1.) 2.) 3.). List the three tRNA anticodons in triplet form. Third base Use the codon map to determine the amino acids coded by the mRNA strand (please use only the abbreviations):
Complete the table below by adding (+) or (-) if eahc sample (amino acid or protein) below will test positive or negative, respectively. sample BIURET NINHYDRIN XANTHOPROTEIC MILLON-NASSE SAKAGUCHI LEAD ACETATE PAULY HOSKIN-COLE G W H Y C R HAIR GELATIN CASEIN PEPTONE Identify the amino acid that will give the following data: BIURET NINHYDRIN XANTHOPROTEIC MILLON-NASSE SAKAGUCHI LEAD ACETATE PAULY HOPSKIN-COLE - + + + - - + - Name of amino acid: structurte of the amino acid:
A vial of Doxorubicin reads 0•5g per vial. Instructions say to reconstitute each 12mg with 2•5ml of NS. How many ml of NS will be needed to reconstitute the vial of the recommended concentration? please show working
In SDS PAGE the resolving gel : is 4%(w/v) acrylamide,PH )6.8 is 6-20% (w/v) acrylamide is 4%(w/v) acrylamide
Image 1 shows raw data of gel electrophoresis. Label/annotate image 1 (lanes, ladder sizes, etc). Explain what your seeing in the gel. Use the following information and picture 2 to assist in labelling. The purpose of this gel electrophorsis is to ensure that your GOI, FAP257, is in each BAC. Protocol that was done for Gel electrophoresis: -Place tray with gel into gel box -Fill gel box with IX TAE until the gel is completely submerged -Remove the comb for wells -Load 10ul of the 1kb Gene Ruler ladder (well 1) -Contains DNA ladder, 6X TriTrack DNA, Loading Dye, and Deionized water -Load other wells -Well 2: Control -Well 3: BAC- 15M5 -Well 4: BAC-39K10 -Well 5: BAC-27N17 -Run the gel at 100V for 30 minutes or until the dye front has migrated 2/3 down the gel
Shortly discuss the above antibodie structure? Please discuss at your own words . Discussion should be to the point (specific 5-6 lines).
Please do not give solution in image format thanku
The SDS-PAGE protocol requires 0.5L of running buffer for the gel apparatus. The stock running buffer comes as a 20x concentrate. How should you prepare your running buffer? 50ml 20x stock + 450ml deionized water 450ml 20x stock + 50ml deionized water O 250ml 20x stock + 250ml deionized water 25ml 20x stock + 500ml deionized water 25ml 20x stock + 475ml deionized water 2ml 20x stock + 500ml deionized water O 100ml 20x stock + 400ml deionized water
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