User:Dhea Patel/Notebook/Hemoglobin Project/2013/02/12: Difference between revisions

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'''Only MeOH and Acetone samples (for both mannitol in tris and p-sorbitol in phosphate) were run today. The rest of the samples will be run [[User:Dhea_Patel/Notebook/Hemoglobin_Project/2013/02/13|tomorrow]].'''
'''Only MeOH and Acetone samples (for both mannitol in tris and p-sorbitol in phosphate) were run today. The rest of the samples will be run [[User:Dhea_Patel/Notebook/Hemoglobin_Project/2013/02/13|tomorrow]].'''
==p-Sorbitol in Phosphate Buffer (after sonication) Data==
*UV-vis of p-Sorbitol solid in MeOH
[[Image:UV-vis_of_9.4mg_psorbitol_Phosphate_Buffer_Solid_in_1mL_MeOH_%28after_sonication%29_.png]]
*Fluorescence of p-Sorbitol solid in MeOH
[[]]
*UV-vis of solid in Acetone
[[Image:UV-vis_of_10.1mg_p-sorbiol_Phosphate_Buffer_Solid_in_1mL_Acetone_%28after_sonication%29_.png]]
*Fluorescence of p-Sorbitol solid in Acetone
[[]]
==Mannitol in Tris Buffer Data==
*UV-vis of Mannitol solid in MeOH
[[Image:UV-vis_of_11.7mg_Mannitol_Tris_Buffer_in_1mL_MeOH_.png]]
* Fluorescence of Mannitol solid in MeOH
[[]]
*UV-vis of Mannitol solid in Acetone
[[Image:UV-vis_of_10.0mg_Mannitol_in_Tris_Buffer_Solid_in_1mL_Acetone.png]]
* Fluorescence of Mannitol solid in Acetone
[[]]


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Revision as of 07:53, 20 February 2013

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Objective

  • Run UV-vis and Fluorescence on p-sorbitol in phosphate buffer and mannitol in tris buffer samples in either MeOH, acetone, acetonitrile, ethyl acetate, water, or chloroform.

Description

  • 11.7mg mannitol in Tris buffer, solvent: MeOH
  • 10.0mg mannitol in Tris buffer, solvent: Acetone
  • 9.4mg p-sorbitol in phosphate buffer, solvent: MeOH
  • 10.1mg p-sorbitol in phosphate buffer, solvent: Acetone
  • all the mannitol in tris buffer samples were vortexed and centrifuged before being measured
  • Centrifuge settings were as follows:
    • 13200rpm
    • 0:16 seconds
    • 851 rotor
  • all the p-sorbitol in phosphate buffer samples were sonicated for 3 hours in their respective solvents.
  • Each solvent was used as a blank.
  • The data was corrected for the blank and a corrected baseline.
  • UV-vis scanned from 200-800nm
  • Fluorescence was run with an emission scan of 310-550nm at an excitation of 290nm and scan speed of 100nm/min.

Only MeOH and Acetone samples (for both mannitol in tris and p-sorbitol in phosphate) were run today. The rest of the samples will be run tomorrow.

p-Sorbitol in Phosphate Buffer (after sonication) Data

  • UV-vis of p-Sorbitol solid in MeOH

  • Fluorescence of p-Sorbitol solid in MeOH

[[]]


  • UV-vis of solid in Acetone

  • Fluorescence of p-Sorbitol solid in Acetone

[[]]


Mannitol in Tris Buffer Data

  • UV-vis of Mannitol solid in MeOH

  • Fluorescence of Mannitol solid in MeOH

[[]]

  • UV-vis of Mannitol solid in Acetone

  • Fluorescence of Mannitol solid in Acetone

[[]]



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