Simplified 2017 Income StatementSimplified 2017 Balance SheetMa.pdf

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Santelle Company expects August sales to be $30,000. Approximately 40% of sales are cash sales. Collection of credit sales are 50% in the month of sale, 40% in the month following sale and 5% two months following sale. The remaining 5% is uncollectible. ________ is the expected cash collection in August from August sales. A) $9,000 B) $12,000 C) $21,000 D) $36,000 Answer: C can you please explain to me how the answer is c? Solution Calculate expected cash collection in august from august sales : so answer is c) $21000AugustCash sales august (30000*40%)12000Credit sales collection (30000*60%*50%)9000Total cash collection in august from august sales21000.

Simplified 2017 Income Statement:
Simplified 2017 Balance Sheet
Management has determined that last year’s ROE (i.e., in 2017) was unacceptable as it
disappointed shareholders. Now, management wants to increase ROE to 20%. Use the DuPont
Decomposition to determine the net profit margin that will be required to achieve this ROE
target. Assume all other ratios in the Dupont Decomposition are held constant. Please show
work.
Solution
Answer:
ROE = Net Income / Shareholders Equity
20% = X / (2500 + 1020 )
X = 3520 x 20% = $704
Net Profit Margin = $704 / $7500 = 9.39%

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Assume a disease is dominant, indicated by shading. Based on the pedigree (click to enlarge), which parent determines whether the child indicated by the question mark will have the disease? Female parent. Male parent. Either parent. Solution Male Parent Because it shows in the pedigree that it is a X-linked disorder. If the child is female definitly she will be diseased getting both the diseased X allele from both the parents. Whereas when the child is male he will get one diseased X allele from mother and normal Y allele from father making him a carrier..

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Chorismate 3-glycero phosphate Relying on the above pathway for bil of tryptophan, fii in the table below to osynthesis predict growth or failure to grow When defective in each of the are placed on media supplemented with the Dom Mutant trpA trpB trpC trpD trpE Supplement Anthranilic acid Tryptophan and indole (Graded as right minus wrong) Solution Suppliment/Mutant trpA trpB trpC trpD trpE None -ve -ve -ve -ve -ve Anthranilic acid -ve - ve -ve -ve +ve Indole -ve +ve +ve +ve +ve tryptophan +ve +ve +ve +ve +ve tryptophan and Indole +ve +ve +ve +ve +ve.

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2.Describe a technique that would allow a developmental biologist to visualize the expression of developmental genes in space and time. Be sure to describe how it works in as much information as you can remember or give an example. 3.Describe (briefly) ONE historical experiment provided by Hans Driesch which refuted the most accepted cell specification mechanism of the time period (1800s). 4.In developmental biology researchers often want to ‘drive’ gene expression within developing tissues – sometimes expressing genes in different locations or at different times of development so as to demonstrate the gene’s role during normal development. What research tools could you use to ‘drive’gene expression of Your Gene of Interest (YGI)? Explain. 5.What does it mean to be genetically equivalent? Describe how cloning demonstrates this? 6.Experiments with Xenopus (frog) in the late 1950s demonstrated that cells within the 3 germ layers had an affinity for each other and thus indicated that they had differentiated enough to be “biased” toward a specific cell layer (endoderm, mesoderm, ectoderm). Describe an experiment that demonstrated how the 3 different layers of the gastrula have an affinity for each other. 7.Morphogenesis involves the orchestration of Cell Affinity, Cell Adhesion, and Cell Migration. How do the adhesive molecules play a role as cells of the embryo change their affinity for one another? please help... Solution The best technique developed to visualise the expression of developmental genes is OPT ( OPTICAL PROJECTION TOMOGRAPHY). It has the ability to generate 3d images of non floroscent signals which helps to capture the expression of gene and histology using traditional tissue strains upto the resolution of 5 um×5um×5um within the 3d context of whole embryo between 0.5 to 15mm in depth. It is quite inexpensive technique , even cheaper than confocal microscopes..

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