Physics307L F07

This is an archive for Physics 307L at the University of New Mexico!

Here is the link to the current course: Physics307L

This site is hosted on OpenWetWare. Many of the links on the left (such as "Main Page") will take you to other OWW pages. Any page that begins with "Physics307L" is a page we have created specifically for this course.

Course times

Lecture:           Mondays    1:00 to 1:50 pm P&A room 184
Labs (choose one): Mondays    2:00 to 4:50 pm P&A room 116
                   Wednesdays 2:00 to 4:50 P&A room 116

Syllabus

See the previous course website for information about the course

The Fall 2007 Physics 307L course (led by Dr. Koch) will be an evolution of the previous semesters led by Dr. Gold. You can find a wealth of information on his website for the course. The experiments offered are likely to be the same as those offered in previous years. (See Schedule for list of experiments.) Any significant changes will be discussed during the first class meeting.

See the Physics and Astronomy website for information on how to register

P&A Fall 2007 Schedule

Recent updates to the course

List of abbreviations:

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26 July 2024

			14:07		UA Biophysics:Equipment‎‎ 3 changes history +48‎ [Elizabeth Suesca‎ (3×)]
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			13:58		(Upload log)‎ [Elizabeth Suesca‎ (2×)]
					13:58 Elizabeth Suesca talk contribs uploaded a new version of File:Spectrofluorimeter.jpg ‎(new)
					13:51 Elizabeth Suesca talk contribs uploaded File:Fluorometro .jpg ‎

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UA Biophysics: Analytical Balance Instructions ESP‎ diffhist +1,106‎ Elizabeth Suesca talk contribs (Created page with "'''Si no tiene autorización para usarlo por favor comunicarse con biofisica@uniandes.edu.co''' '''Al momento de usar este equipo verifique el estado en que lo encuentra. Si el equipo no está en condiciones óptimas debe reportarlo y abstenerse de usarlo. ''' <h2>Uso de la balanza</h2> #La balanza solo debe ser usada para pesar materiales solidos o líquidos en recientes bien cerrados. #Esta balanza no se usará para pesar medios de cultivo celular. #El peso (materi...")

09:58

UA Biophysics: Lyophilizer ESP‎ diffhist +15‎ Elizabeth Suesca talk contribs

09:57

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			N    09:33		UA Biophysics:Protocols:YPD 1L‎‎ 2 changes history +486‎ [Elizabeth Suesca‎ (2×)]
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			N		09:20 (cur | prev) +123‎ Elizabeth Suesca talk contribs (Created page with " <br> YPD_ESP<br> Return to Protocols<br>")

			N    09:30		UA Biophysics:Protocols:YPD ESP‎‎ 3 changes history +476‎ [Elizabeth Suesca‎ (3×)]
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			N		09:28 (cur | prev) +467‎ Elizabeth Suesca talk contribs (Created page with "'''YPD 1L''' ''' Materiales:''' *10 G de extracto de levadura *20 G de peptona *Si hace placas, agregue 20 g de agar *Solución de glucosa filtrada al 40% p/v (20g en 50 ml de agua destilada, caliente para diluir). '''Protocolo:''' *Mezcle los ingredientes secos y agregue agua destilada hasta 950 ml *Autoclavar *Añadir los 50 ml de la solución de glucosa para obtener una concentración final de 2% (p/v). Return to Protocols<br>")

			09:18		UA Biophysics:Protocols‎‎ 3 changes history +123‎ [Elizabeth Suesca‎ (3×)]
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			N    09:14		UA Biophysics:Protocols:Glass Cleaning ESP‎‎ 2 changes history +1,259‎ [Elizabeth Suesca‎ (2×)]
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			N		08:34 (cur | prev) +1,268‎ Elizabeth Suesca talk contribs (Created page with "Limpieza laminillas con Solución piraña '''Materiales:''' • Ácido sulfúrico H2SO4 • Peróxido H2O2 al 50% • Isopropanol '''Procedimiento:''' '''Día 1:''' En cabina de extracción con guantes de nitrilo de alto calibre: *En un vaso de 25 ml de vidrio preparar 20 ml de Solución H2SO4: H2O2 al 30% agregando el peróxido al agua (8 ml de agua y 12 ml de peróxido). *En vaso de 250 ml colocar 60 ml de Ácido sulfúrico *Se le agregan los 20 ml del peróxido m...")

			N    09:13		UA Biophysics:Protocols: Glass Cleaning‎‎ 2 changes history +1,271‎ [Elizabeth Suesca‎ (2×)]
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			N		08:28 (cur | prev) +760‎ Elizabeth Suesca talk contribs (Created page with "== Materials == == Protocol == *The samples are dissolve in a mixture of chloroform/methanol/water (3:6:1 v/v):<br> Add chloroform, vortex 5 minutes<br> Add methanol vortex 5 minutes<br> Add water vortex 1 minute<br> and then vortexed every 15min for 4h(solution have to be homogeneous<br> *The samples are then allowed to stand for 2 days to separate the three phases, after which the lower phase of chloroform and lipid is drawn off by aspiration and collected in a clean...")

25 July 2024

14:22

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24 July 2024

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23 July 2024

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