Physics307L

This is the homepage (wiki) for Physics 307L at the University of New Mexico.

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. Everything we do for the course, except confidential letter grades, are carried out in public on this wiki. This includes primary lab notebooks, summaries, formal report rough and final drafts, and all of the instructor feedback. Thus, we're carrying out open science and we're enjoying it. One of the best results of this open science course is that students have been reading and citing each other's work and learning how to be open scientists at a very early point in their careers.

If you're a visitor to the course and wondering how it works, here are some suggested links

• Physics307L:People. Since this is an open science course, the people in the course are the most important part and they create the content. From this page, you can click on a student's "my page for the course" to find their notebook, summaries, and formal reports. Most of the students have created a bunch of very good work to look at. Here is a link to one of the best students: Physics307L:People/Klimov
• Course Goals. These goals need to be revised, but you can get an idea of what we're trying to achieve here.

Course times

Lecture:           Mondays    1:00 to 1:50 pm P&A room 5
Labs (choose one): Mondays    2:00 to 4:50 pm P&A room 135
                   Wednesdays 2:00 to 4:50 P&A room 135

Syllabus

See the Prof. Gold's lab manual for information about the experiments

The Fall 2008 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 2009 Schedule

Recent updates to the course

List of abbreviations:

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6 June 2023

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5 June 2023

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User creation log User account Ruaidhri talk contribs was created by Yar talk contribs and password was sent by email ‎

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4 June 2023

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3 June 2023

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1 June 2023

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31 May 2023

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UA Biophysics:Protocols:Carotenoid Extration ESP‎ diffhist +423‎ Elizabeth Suesca talk contribs (Created page with "==Materiales para 6 gramos de célula== * Preparar centrífuga a 4 grados * 200 ml Metanol. Opcional: Agregar 2,6-Di-tert-butyl-4-methylphenol 0.1 % w/V (250 mg/250 ml) Para la extracción de carotenos, ya que los protegen de oxidación * 500 NaCl 1,7 M (99.348 g/1 L) * 200 Acetato de etilo (Mejor si esta destilado ya que tiende a ser muy hidrófilo) * Opcional Na2SO4 anhidro (1 g/ 500 ml de solución) * Cloroformo")

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			N		14:07 (cur | prev) +588‎ Elizabeth Suesca talk contribs (Created page with " '''Buffer HEPES: 2 L a 400 mOsM pH 7.4 ==Materiales== MW (g/mol) [] mM mOsM M HEPES 238.30 20 20 9.532 g NaCl 58.44 170 340 19.869 g NaOH (1 M) 8 8 16 ml NaCl 16 32 1.870 g Colocar 1.6 litros de agua deionizada en la botella Pesar el HEPES y el NaCl, diluir en los 1,6 L de dH2O Ajustar pH usando NaOH a 7.4. Calcular la osmolaridad y completar los 400 mOsm con NaCl Completar los dos litros UA Biop...")

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			N		14:00 (cur | prev) +1,143‎ Elizabeth Suesca talk contribs (Created page with "'''Calceina: 400 mOsM, 50 mM, 100 ml, pH 7.4 ''' ==Materiales: == * Probeta 100 ml * 30 ml de NaOH (1M) * HCl (1M) * 3,113 g de calceina * 40 ml Buffer H: ** 5 ml de EDTA 0.2 mM (Para que quede a 0.01 mM en la solución final) ** HEPES 238.3 mg (para que quede a 10 mM en la solución final). ==Procedimiento: == # En la probeta medir 20 ml de NaOH 1M y colocar agitador # Disolver en el NaOH 3,113 g de calceina # Agregar los 40 ml del Buffer H a la calceina # A...")

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UA Biophysics:Protocols:Bacteria for Lipid Extraction ESP‎ diffhist +1,206‎ Elizabeth Suesca talk contribs (Created page with "==Materiales para 1.4 g de célula== * Plato con SA401, máximo de un mes desde la recuperación <br> * Frasco de vidrio con 10 ml de LB<br> * 2 L de LB repartidos en 13 Erlenmeyer de 500 ml<br> ==Procedimiento== '''Dia 1''' 4:00 pm ON de SA401: una colonia en el frasco con 10 ml de LB. <br> '''Dia 2''' 8:30 am Dilución de las células: 10 ul en cada Erlenmeyer<br> '''Dia 3''' 8:30 am Concentrar la muestra <br> * Prepara la centrífuga a 4°C. <br> * Refrigerar lo...")