User:Moira M. Esson/Notebook/CHEM-571/2013/09/17

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(HRP Oxidation)
(HRP Oxidation)
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Table 1: Sample preparation for HRP
Table 1: Sample preparation for HRP
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{| {{table}}
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| align="center" style="background:#f0f0f0;"|'''Dilution'''
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| align="center" style="background:#f0f0f0;"|''''''M<sub>1'''[μM]'''
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| align="center" style="background:#f0f0f0;"|''''''V<sub>1''' [mL]'''
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| align="center" style="background:#f0f0f0;"|''''''M<sub>2'''[μM]'''
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| align="center" style="background:#f0f0f0;"|''''''V<sub>2''' [mL]'''
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| 1||17.25||.580||10||1||
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|}
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*Added .419mL of buffer to reach a volume of 1mL.

Revision as of 13:26, 17 September 2013

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Objectives

  1. Find endpoints (100%) of oxidation and reduction of HRP


HRP Oxidation

General Protocol:

  1. Run UV-vis of a blank buffer sample.
  2. Prepare a 1mL sample of 10μM HRP in 50Tris, 50Nacl, pH=7.5 buffer. This buffer should be degassed) directly in a clean glass cuvette.
  3. Take spectrum of the prepared 10μM HRP sample.
  4. Add 2μL of K3[Fe(CN)6] to the prepared sample.
  5. Take UV/vis spectrum of the sample.
  6. Repeat steps 4-5 until complete oxidation of HRP.
    • Note: When preparing the sample add all components 'very slowly
    • Note: Allow all samples to sit for approximately 5 minutes before taking the spectrum
    • Note: No more than 20uL should be added of the K3[Fe(CN)6] to the sample.


Table 1: Sample preparation for HRP

Dilution 'M1'[μM] 'V1' [mL] 'M2'[μM] 'V2' [mL]
117.25.580101
  • Added .419mL of buffer to reach a volume of 1mL.


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