Professional Documents
Culture Documents
Marking Scheme:
- Do not include basic techniques (i.e. spreading until the plate is dry; placing the plates upside
down); deduce 0.5 for every unnecessary detail up to 2 pt. 1/2
-
- Do not include unnecessary details (container used, tool used); deduce 0.5 for every
unnecessary details up to 2 pt 0/2
-
- Do not start with a verb or a number. Do not use a personal tone; Deduce 0.5 point for each
instance up to a max for 1 pt 1/1.5
-
- Explain controls; 0.5 in the body of the text (must be after the description of the experimental
group); 0.5 correctly describe the positive control; 0.5 correctly describe the negative control.
0/1.5
-
- Explain what the steps are for; 0.5 45s at 42oC for heat shock; 0.5 add LB for cell recovery/gene
expression. 0.5/1
-
- Include a sentence analysing the results; 1 sentence well written; 0.5 sentence need
improvement; 0 no analysis. 0.5/1
-
- Intro sentence: 1 the intro sentence is well written; 0.5 there is intro sentence but needs
improvement; 0 there is no intro sentence. 0.5/1
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- Key words; 0.5 for each (plasmid; bacteria are not appropriate key words) ; 0 if incorrect or no
key words. 0/1.5
-
- Media with reference or source (e.g Miller 1972 or Thermo Fisher + others). 0/0.5
-
- Plasmid name with reference; 0.5: pRSET-FPx; 0.5 Shaner et al., 2004. 0/1
-
- Reference; should have at least 1; 1 for properly referencing APA style; 0.5 if not in APA style; 0
for no references or for citing the lab manual or for providing references not cited in the text or
that are irrelevant. 0/1
-
- Strain name with source: 0.5 E. coli JM109-DE3; 0.5 Promega corporation. 0.5/1
-
- Subtitle: 1 for non descriptive tilte (only techniwue's name ; 0.5 for descriptive title; 0 for no
subtitle. 0.5/1
-
- Title page: 2 well written an cover the whole semester; 1 if it is too general; Deduce 0.5 if they
mention M&M; 0 if it is incorrect or they do not have a title ½
- The first sentence (or part of the sentence) of each section must
explain what a particular procedure is for (for example; Genomic DNA was extracted
- It should therefore contain all pertinent technical details, the instruments used and experimental
variable (e.g. temperature, incubation time, masses, sizes and volumes, concentrations, voltage,
type and % of gel, markers used, centrifuge time and speed, etc.). You should also indicate
what the different steps are for.
- do not mention details of standard and generally known procedures (i.e. size
of the flask used; that you used a marker to label the tubes; how to use a microscope
or a centrifuge; how to perform dilutions, etc.).
- reference an
article in the M & M section is the same as what you would do in the Introduction and
Discussion sections: for one author (Smith, 2018); for two authors: (Smith and John,
2005); for more than two authors (John et al., 2014). Note that “et al.” is always written in italic.
Make sure to also include the full reference in the reference section
• Types of treatment
• Number of replicates
• Controls used
• Variables measured
brackets). This information is only required for the specialized type of equipment
• Describe the composition of the solutions used. If the solutions are standard and
have been described in another publication, cite the publication instead of writing
• Explain how the data were collected and analyzed (statistical analysis, calculation