Decision Sheet Of The Year No Price

Decision Sheetperiod Of Yearperiod Noprice

Decision Sheet period of year period no. price $ marketing budget $ r & d budget $ maintenance budget $ prod vol. sch. maximums: model 1 1.4*CY1 units investment in robotics $ investment in plant & equipment $ purchase of materials $ dividend declared (max; owner's equity minus $9,000,000 $ AMJ 0 25.,,,,,,000,,000 JAS T1 25.,,,,,,000,,000 OND T2 24.,,,,,,,000 AMJ 0 25.,,,,,,000,,000 JAS 1 24.,,,,,,000,,000 OND 2 - JFM 3 - AMJ 4 - JAS 5 - OND 6 JFM 7 AMJ 8 average 25.,,,,,,000,,500 period of year AMJ JAS OND AMJ JAS OND JFM AMJ JAS OND JFM AMJ period no. 0 T1 T forecast, econ. index changes (if any) forecast, seasonal index changes (if any) T1 T price index fcst, annual change econ index fcst, nxt qtr seasonal index next quarter averages pd 1-3 trial 1 firm no. price dividends sales volume net profit ROI period 1 firm no. price dividends sales volume net profit ROI 1 24.,,,..,,,..,,,..,,,..,,,. average 25.,,,.01 average 0..00 trial 2 firm no. price dividends sales volume net profit ROI period 2 firm no. price dividends sales volume net profit ROI 1 22.,,,..,,,..,,,..,,,..,,,. average 24.,,,.30 average trial 3 firm no. price dividends sales volume net profit ROI period 3 firm no. price dividends sales volume net profit ROI average 0..00 average ages pds 4-8 period 4 firm no. price dividends sales volume net profit ROI period 7 firm no. price dividends sales volume net profit ROI average 0..00 average period 5 firm no. price dividends sales volume net profit ROI period 8 firm no. price dividends sales volume net profit ROI average average period 6 firm no. price dividends sales volume net profit ROI average original sheet step 1 P0 P1 #change %change given totalchange econ .4 0 seas ..05 ourprice 25..6 -0.. comprice 25..4 0..03125 ourmart ...00625 compmark .5 -0.1 -0.05 total change 0. MPP changP0P.8125 MPP.8125 step 2 stockout MPP salesp sales loss 0 adjMPP.8125 step 3 did you like the results? step 4 adjMPP.8125 $2,858,720.31 FGI 12750 need to produce 101598.8125 step 5 rmi $1,200,000 cpu $6.31 pfg 190174. step 6 plcP OT 146500.2 effic 0. step 7 produce 101,599 leftover pfg 88,576 for period 2 step 8 P1 P2 #change %change given totalchange econ .05 1.4 -0.07 seas .. total change 0. adjMPP.8125 estMP. leftover pfg 88,576 for period 2 min order P.32 cpu $6.31 ordermin $264,025.01 step 9 plcP depreciation do nothing 101268.% 3374.73675 inflation status quo $ 236,231..25% add units 1000 cost $ 70,000.00 total inv $ 306,231.57 step 10 produce 101,599 cost main $ 76,199.11 $ 0.75 maintenance trial 1 step 1 P0 P1 #change %change given totalchange econ .4 0 seas ..05 ourprice 25.6 25.3 -0.3 -0.. comprice 25..4 0..03125 ourmark .25 0.25 0.0625 compmark .5 -0.1 -0.05 total change 0. P1 P.15625 MPP changeP0P.15625 MPP step 2 stockout MPP salesp sales loss 0 adjMPP step 3 did you like the results? step 4 adjMPP.2 $2,921,217.85 FGI 12750 need to produce 102713.2 step 5 rmi $1,200,000.00 cpu $6.31 pfg 190174. step 6 plcP OT 146500.2 effic 0. step 7 produce 102,713 leftover pfg 87,461 for period 2 step 8 Period 1 P2 #change %change given totalchange econ .05 1.4 -0.07 seas .. total change 0. adjMPP.2 estMP.8 leftover pfg 87,461 for period 2 min order P.60 cpu $6.31 ordermin 279076.1 step 9 plcP depreciation do nothing 101268.% 3374.73675 inflation status quo 236231..25% add units 1000 cost $ 70,000.00 total inv $ 306,231.57 step 10 produce 102,713 cost main 77034.87 $ 0.75 maintenance trial 2 step 1 P1 P2 #change %change given totalchange econ ..4 -0. seas .. ourprice 25.3 24.6 -0.7 -0.. comprice 25..4 0..03125 ourmart .4 0.25 0.1 compmark .5 -0.1 -0.05 total change 0. P1 P.3125 MPP changeP1P. MPP step 2 stockout MPP salesp sales loss 0 adjMPP step 3 did you like the results? step 4 adjMPP $3,921,882.13 FGI 159426 need to produce 159426 step 5 rmi $1,552,346.00 cpu $6.31 pfg 246013.629 step 6 plcP OT 153472.2 effic 1..4 or below step 7 produce 159,426 leftover pfg 86,588 for period 3 step 8 Trial 1 Trial 2 #change %change given totalchange econ .05 1.4 -0.07 seas .. total change 0. adjMPP.103 estMP. leftover pfg 86,588 for period 3 min order P.14 cpu $6.31 ordermin 600977.90 step 9 plcP depreciation do nothing 106087.% 3535.34175 inflation status quo 247473..25% add units 1000 cost 70000.00 total inv 317473.92 step 10 produce 159,426 cost main 119570 $ 0.75 maintenance period 3 step 1 P2 P3 #change %change given totalchange econ .4 0 seas ..05 ourprice 25..6 -0.. comprice 25..4 0..03125 ourmart ...00625 compmark .5 -0.1 -0.05 total change 0. P2 P.8125 MPP changeP2P.8125 step 2 stockout MPP salesp sales loss 0 adjMPP.8125 step 3 did you like the results? step 4 adjMPP.8125 $2,858,720.31 FGI 12750 need to produce 101598.8125 step 5 rmi $1,200,000 cpu $6.31 pfg 190174. step 6 plcP OT 146500.2 effic 0. step 7 produce 101,599 leftover pfg 88,576 for period 2 step 8 P3 P4 #change %change given totalchange econ .05 1.4 -0.07 seas .. total change 0. adjMPP.8125 estMP. leftover pfg 88,576 for period 2 min order P.32 cpu $6.31 ordermin $264,025.01 step 9 plcP depreciation do nothing 101268.% 3374.73675 inflation status quo 236231..25% add units 1000 cost $ 70,000.00 total inv $ 306,231.57 step 10 produce 101,599 cost main $ 76,199.11 $ 0.75 maintenance period 4 step 1 P0 P1 #change %change given totalchange econ .4 0 seas ..05 ourprice 25..6 -0.. comprice 25..4 0..03125 ourmart ...00625 compmark .5 -0.1 -0.05 total change 0. P0 P.8125 MPP changeP0P.8125 step 2 stockout MPP salesp sales loss 0 adjMPP step 3 did you like the results? step 4 adjMPP.8125 $2,858,720.31 FGI 12750 need to produce 101598.8125 step 5 rmi $1,200,000 cpu $6.31 pfg 190174. step 6 plcP OT 146500.2 effic 0. step 7 produce 101,599 leftover pfg 88,576 for period 2 step 8 P1 P2 #change %change given totalchange econ .05 1.4 -0.07 seas .. total change 0. adjMPP.8125 estMP. leftover pfg 88,576 for period 2 min order P.32 cpu $6.31 ordermin $264,025.01 step 9 plcP depreciation do nothing 101268.% 3374.73675 inflation status quo $ 236,231..25% add units 1000 cost $ 70,000.00 total inv $ 306,231.57 step 10 produce 101,599 cost main $ 76,199.11 $ 0.75 maintenance Period 5 step 1 P0 P1 #change %change given totalchange econ .4 0 seas ..05 ourprice 25..6 -0.. comprice 25..4 0..03125 ourmart ...00625 compmark .5 -0.1 -0.05 total change 0. P0 P.8125 MPP changeP0P.8125 step 2 stockout MPP salesp sales loss 0 adjMPP.8125 step 3 did you like the results? step 4 adjMPP.8125 $2,858,720.31 FGI 12750 need to produce 101598.8125 step 5 rmi $1,200,000 cpu $6.31 pfg 190174. step 6 plcP OT 146500.2 effic 0. step 7 produce 101,599 leftover pfg 88,576 for period 2 step 8 P1 P2 #change %change given totalchange econ .05 1.4 -0.07 seas .. total change 0. adjMPP.8125 estMP. leftover pfg 88,576 for period 2 min order P.32 cpu $6.31 ordermin $264,025.01 step 9 plcP depreciation do nothing 101268.% 3374.73675 inflation status quo $ 236,231..25% add units 1000 cost $ 70,000.00 total inv $ 306,231.57 step 10 produce 101,599 cost main $ 76,199.11 $ 0.75 maintenance statements xgame practice.

period 1. model no. 1 price index 102.5 fcst, annual change 5 econ index 94 fcst, nxt qtr 93 seasonal index 115 next quarter 90 operating statement for firm 2 market potential 101,311 sales volume 101,311 percent share of industry sales 13 production volume (this year) 107,257 closing inventory of finished goods (units) 16,111 plant capacity, quarter 2 (next quarter) 109,279 income statement total revenue (sales revenue) 2,556,082 expense marketing 150,000 r&d 120,000 administration 288,223 maintenance 80,443 labor (regular time cost/unit 5,922 raw materials consumed (cost/unit 6,565 reduction, finished goods inventory 73,722 plant+eq depreciation (%change rate/qrt 2.,120 robotics depreciation (%change rate/qrt 0.

finished goods carrying cost 32,618 raw material carrying cost 42,763 ordering costs 50,614 plant investment expenses 6,470 financing charges and penalties 0 sundry expense 87,802 total expenses 2,234,816 profit before income tax 321,266 income tax or refund (inv. credit 0.0%; surtax 0.0%) 109,230 net profit after income tax 212,036 dividends paid 51,500 addition to owners' equity 160,536 cash flow total receipts (sales revenue) 2,556,082 disbursements cash expense 1,482,853 net income tax payment 109,230 dividends paid 51,500 robotics investment 0 plant investment 254,354 materials purchased 310,000 total disbursements 2,207,938 net addition to cash 348,144 financial statement cash assets 1,692,313 inventory value, finished goods 195,705 inventory value, raw materials 490,690 robotics book value 0 plant + equipment book value 7,659,244 owners' equity 10,037,950 robotics replacement value 0 plant + equipment replacement value 7,838,420 owners' economic equity 10,217,130 test problem set: 1. generate a genetic system of: a) inactivation (15 pts) b) transfer (15 pts) of any E. coli. gene selected by dr. roberts, and using transduction imagine dr. roberts telling you: "student, i need to inactivate gene x of e. coli using transduction" or "i need to transfer the gene x from this e. coli to another, by transduction" client" note: every time genetic system is mentioned, it refers to a laboratory assay or study 2. generate a genetic system for gram-positive that (based on the genetic material transference mechanisms): a. that allow us to know that the bacterial community is conducting quorum sensing. (10pts) b. that allows that during the logarithmic phase, the bacteria eliminates bacteria a (who is sensitive to chloramphenicol); and during the stationary phase, the bacteria eliminates bacteria b (who is sensitive to tetracycline). (15pts) 3. a bacteria posses a plasmid with: resistance gene to chloramphenicol (cat), an indispensable gene for starch degradation (amiA), and another gene for lactose degradation (lac z). for this bacteria, the genetic transference systems and is (insertion sequences) are unknown. design and demonstrate, making sure to include specific verification systems: a. a bacteria able to transfer lacZ gene via conjugation (10 pts) b. development of bacteriophages capable of transferring amiA gene or a portion of amiA gene via transduction (10 pts) 4. design an experiment that allows me to determine if a pair of genes or isolated dna fragments, encodes for the following (bioinformatics, southern, antibodies or probes can't be used) (20pts): a. clpc vs λd gal b. degs vs trai 5. develop and present an ideal plasmid that could be used for dr. smith, dr. rose and dr. spencer investigations. remember to use plassmapper (free program to create the image/figure of the plasmid). (15pts) "client" note: at the moment i'm searching the information related to the type of investigations those 3 professors are conducting or have in common

Paper For Above instruction

The detailed assignment involves understanding genetic systems in bacteria, specifically focusing on mechanisms such as inactivation and transfer of genes in E. coli, quorum sensing in gram-positive bacteria, gene transfer via conjugation and transduction, and designing experimental approaches to determine gene encoding functions, along with creating a comprehensive plasmid vector suitable for multiple research investigations. These tasks necessitate integrating molecular genetics principles, microbiological techniques, and bioinformatics tools to achieve precise genetic manipulations and functional verifications in microbial systems. The aim is to demonstrate proficiency in bacterial genetic engineering, understanding of gene transfer mechanisms, and plasmid design tailored to specific research requirements.

In the first part, you are asked to design a genetic system for E. coli for gene inactivation and transfer via transduction based on Dr. Roberts' instructions. For gene inactivation, you might employ temperate bacteriophages carrying a disrupted gene or insertions that hinder gene expression. For gene transfer, using generalized transduction with bacteriophages, you can package bacterial DNA (containing the gene of interest) into phage particles and infect recipient cells to integrate the gene. These systems would involve creating mutant strains or recombinant phages, verifying gene disruption or transfer with phenotypic assays, PCR, or selectable markers.

The second task involves establishing a genetic system for gram-positive bacteria to monitor quorum sensing, such as fusing a reporter gene (like GFP or luciferase) under the control of quorum sensing-regulated promoters. Additionally, designing a system that during exponential growth phase produces enzymes that eliminate bacteria sensitive to specific antibiotics at different stages can be achieved with inducible promoters modulating bacteriocin production.

Thirdly, the creation of gene transfer systems for a plasmid bearing antibiotic resistance genes and catabolic genes involves understanding conjugation and transduction mechanics without existing insertion sequences knowledge. For conjugation, engineering a conjugative plasmid with tra genes and verification via mating assays and selective media is essential. For transduction, developing bacteriophages capable of packaging and transferring the specific gene segments of amiA gene requires isolation and engineering of lysogenic phages and verifying successful transfer by selecting for antibiotic resistance or metabolic activity.

Fourth, you must devise an experimental setup to confirm whether certain gene pairs or DNA fragments code for specific proteins, without using bioinformatics tools or molecular probes. This can involve functional complementation assays, activity tests, phenotype analysis in mutant strains, or enzymatic activity assays to correlate gene presence with function.

Lastly, designing an ideal plasmid involves incorporating features such as multiple cloning sites, origins of replication optimized for different hosts, selectable markers, and reporter genes. Using PlasmidMapper to visualize the construct ensures a functional, versatile vector suitable