trouble-shooting
DESCRIPTION
Trouble-shooting. (also a science). Things that didn’t go as expected. Gold color did not disappear over 2 hour time rocking at room temperature After reduction and silver step, purple color did not develop Are there nanowires? What happened??. Clear – what it is supposed to look like!. - PowerPoint PPT PresentationTRANSCRIPT
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Trouble-shooting.
(also a science)
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Things that didn’t go as expected • Gold color did not disappear
over 2 hour time rocking at room temperature
• After reduction and silver step, purple color did not develop
• Are there nanowires? What happened??
Dark orange – something’s not right
Gold – after two hours of rocking
Clear – what it is supposed to look like!
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“Low hanging fruit”
• Phage titered correctly? Concentrations calculated correctly?– T/R lab, John and Bridget went through all of your
notebooks looking for these calculations – This is why you always right neatly and make sure
to read directions! Only one group remarked on the color change that took place.
– End result: even if there were slight calculation errors, all the phage added into the reaction mixture is in the correct order of magnitude
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Too much gold for the ascorbic acid?
• Calculated the number of gold particles (based on molarity of gold solution)
• Calculated the number of nucleation sites (based on concentration of phage and number of p8 proteins)
• Phage reduces the gold that binds to the mutated p8 protein
• Calculated amount of ascorbic acid able to reduce the extra free gold in solution (if there weren’t enough phage)
• End result: reducing power is still in excess – this shouldn’t be a problem
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Problem of “cutting corners * 1000”
• If we are an order of magnitude off in terms of phage and an order of magnitude off in terms of gold, does this make the experiment just fail?
• End result: Maybe, but nothing so drastic. This “cutting corners * 1000” is more likely to have an effect on the nanoscale and create nanoparticles instead of nanowires…it isn’t something that would change how we’d see the color change
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Contamination?
• Belcher Lab has had issues with E4 contamination in the past– Remember E4?
• Normally perform a DNA sequencing analysis to check on this– How could this experiment be done?
• End result: phage contamination would not change the goldclear or the purple color change, so this isn’t contributing to our problem
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pH?
• What if the pH of both the water and TBS is off? – Nanopure water vs. DI water
• End result: pH of both Belcher solutions and 20.109 solutions were similar (within 0.01)
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What about the other solutions?
• Hmm, that gold looks sort of dark…• Absorbance on a spectrophotometer• Gold solution used T/R was significantly
darker (error in solution-making?)• Bridget re-made gold solution for W/F lab• Is this it??
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Gold color didn’t disappear. Again. Now what?
• What about TBS? I mean, it’s a standard buffer, right?
• Apparently not. . .
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Ionic Strength
General Equation: or
Biorad 1xTBS: pH = 7.5 0.020M TBS 0.5M NaCl
Rockland 1xTBS: pH = 7.5 0.1M TBS(HCl) 0.15M NaCl
Therefore,
IBiorad TBS = 0.518
IRockland TBS = 0.241
Qualitatively increased ionic strength results in:• Increased ionic charge shielding• Decreased ionic mobility (and diffusivity)
These factors should:•Decrease the ability of gold ions to penetrate CTAB bilayer• A high [NaCl] might lead to Na+ binding at p8