Sigmaplot Exercise How To Graph Data
Sigmaplot Exercise How To Graph Data
This exercise mimics the research experience (I recommend that instead of asking me what to do next,
that YOU discover how to overcome obstacles). Thus, THIS EXERCISE TESTS YOUR DRIVE,
INGENUITY, INITIATIVE AND PERSEVERANCE! BE CLEVER TO OVERCOME
CHALLENGES! Many of experiments in this Cell Bio/Mol Bio lab are like real research- there may
be a variety of correct answers or methods. Like real research, you must think of ways to overcome
problems, develop methods and come up with the answers independently (e.g., how to record the
distance proteins travel in the gel, find help on the web, in SigmaPlots help manual, etc.).
Recommended steps for lab experiments: (1) define problems (what you need to do), (2) how to
address problems; brainstorm solutions (3) evaluate collected data (you have to answer
the question of how to do this?).
Fight procrastination (do you continue to ask me questions that you should answer?);
jump right in, avoid excuses. Independent thinkers will proceed faster.
Begin your use of SigmaPlot by following the directions below. Open the program on
your computer and remember to save your data as you go along. Put your data on a
floppy or flash drive, or email it yourself.
The SigmaPlot help manual can be accessed from within the program, or go to this web
site: http://www.cof.orst.edu/net/software/sigplot/workshop.php
Information for graphing, scanning, presentations:
http://bama.ua.edu/~hsmithso/class/bsc_695/links/index.shtml
TIP: click on something in the graph or highlight data that you want to change.
Plot the data shown in Fig. 2-9 instead of Fig. 2-8 (later is not shown).
Next, learn how to manipulate data in the table: switch the Y value for the two X values
of 6 and 8. Then, add a Y value for 12: 14.
Print off the figure you generate.
Next, change the Y axis to log (not linear); try double clicking on the axis and then
clicking on SCALING, and then on the new page pick SCALE TYPE and change to
LOG.
Note that you have transformed the curved line to a straight line. Next, find the
regression line (equation of the line defined by the numbers). Click on STATISTICS,
LINEAR REGRESSION. Click on All data in plot, and Extend to axes. Click on
APPLY. Then click on RESULTS, and look for the following:
All curves:
Coefficients:
b[0] 0
b[1] 0.0927183211
b[0] stands for the y intercept of the equation Y = mx + b
b[1] stands for the slope m
(if you have an X2 term, you would find a number listed as b[2] for the number associated
with X2).
What does the r value mean? (r or R ranges from 0 to 1, 0.9 to 1 means good data; .4 or
below means redo the experiment)
Print off the linear form of the graph that shows the regression line.
Thus, if you have a new X value, you can calculate the Y value from the equation (do
this- pick a number such as 15). Double check your answer by using the graphs that you
printed out. This may be a process upon which I will test on upcoming exams.
Dont forget to save your data. In addition to printing off graphs, you should bring
floppies or flash drives to future labs to copy your data; or send you files to yourself by
email.
5. As the proteins make their way through the channels (or caves) in the gel, the
smaller proteins move with less resistance- thus move faster than the bigger
proteins. (longer migration for smaller proteins)
6. This separates the proteins by size. Standard proteins (proteins of known weight)
are added to other lanes, so we can find out how big our unknown protein of
interest is by comparison.
Read your text (see below) & the directions given below, but first look at this web site:
http://www5.amershambiosciences.com/aptrix/upp00919.nsf/(FileDownload)?OpenAgen
t&docid=2343097446FC389FC1256EB400417D11&file=11B06413.pdf
Using the SigmaPlot program, graph the following (X, Y) data from Fig. 7-22
of the text:
Spectrin: 280,000 Daltons (Dalton is a measure of size; it is the weight of a
proton)
Anion Exchange Protein: 96,000 Daltons; Actin is 43,000 Daltons. Use semilog plot.
How big are GPD and Ankyrin? Record all details of how you got the answer
and the calculations themselves in your lab notebook.
You need some information to find the answers; first,
Read the manual for a protein standard kit:
http://www.piercenet.com/Products/Browse.cfm?fldID=02051027
Follow the instructions for the standard protein marker kit:
In summary, what you want to do; measure how far all proteins migrated from
the top of the gel. With the standard protein sizes noted above, plot out with
SigmaPlot (you have to use semi-log), print off for your lab notebook. Find
the numerical values for the standard line (y=mx + b but SigmaPlot uses the
format of y= (2)X + (1)) using SigmaPlots regression line program. Calculate
the size of the unknown proteins by plugging their migration value into the
equation and record this in your lab notebook.
Transfer graphs that you generate in SigmaPlot to a Word file: on the graph
page, go to EDIT and SELECT ALL, then hit control-S to save. Then open a
Word document and hit control-V to paste the SigmaPlot graph into the
document. Now you can add text around the figure. From within Word: if
you want to move the figure to the right side of the page, right click on the
figure and change its properties.
Use the SigmaPlot Program to analyze the data below with a t Test:
Control
Experimental group
55.2000
70.0000
62.4000
66.0000
58.0000
71.0000
61.0000
69.0000
66.0000
67.0000
Enter the data into a new file (name it and save it), then click on Statistics and
(Pooled) t Test or Paired t Test. Analyze the data both ways and tell me if
there is a significant difference between the two groups (you will get two
different P values; record them with the appropriate t Test).
Read the following section on SDS Polyacrylamide Gel Electrophoresis from World of
the Cell (6th ed): (tip: a test may ask you to define what SDS is)
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You can open Excel spreadsheets directly inside SigmaPlot, allowing you to use the
many features Excel offers. Use in-cell formulas and other Excel data analysis tools on
your data.
One-click access to directly launch SigmaPlot from Microsoft Excel
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Symbol Types
Enter colors, patterns, symbols, line styles, tick mark intervals, tick labels and more
directly into your worksheet to customize your graph the way you want. Transforms and
"picking from column" allow you to create data dependent color gradients, symbols and
sizes.
SigmaPlot Notebook
Import
Axon Binary, Axon Text, ASCII Plain, Comma and general import filter, 1-2-3T,
Symphony T, Quattro T, Excel, dBASE E, DIF, SigmaPlot for DOS 4.0, 4.1, 5.0,
SigmaPlot 1.0, 2.0, and 3.0, 4.0, 5.0 for Windows, SigmaPlot 4.1 and 5.0 for Macintosh
data worksheets, SYSTAT, SigmaScan Pro, SigmaScan, SigmaScan Image, Mocha
Import and ODBC compliant database
Run SQL queries on tables and selectively import information
Export
ASCII Text, Tabbed, Comma, 1-2-3T, Excel, DIF, SigmaPlot 1.0, 2.0, and 3.0 for
Windows, SigmaPlot 5.0 for Macintosh data worksheets, SigmaScan Pro
PDF and HTML export of graphs and reports
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Windows Application
Excel, Word and PowerPoint for Office 2000 and Windows 2000 support ToolTips
Tips and Tricks at startup
Full 32-bit implementation
OLE 2 container and server
Use Excel worksheets inside SigmaPlot
Uninstaller
Controls have bitmaps to give feedback about selections
Right mouse button property editing
Selection of objects on graph page
Full precision and date/time Microsoft Excel copy and paste
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