Fanconi Anemia Research Community
In progress
Welcome to the Fanconi Anemia Research Community <wikionly>wiki</wikionly><nonwikionly>website.</nonwikionly>. We are researchers interested in understanding how the Fanconi anemia proteins contribute to the maintenance of genomic stability with the goal of developing better treatments for Fanconi patients. |
AnnouncementsTwentieth Annual Fanconi Anemia Scientific Symposium The Twentieth Annual Fanconi Anemia Research Fund Scientific Symposium will be held from 3pm, Saturday, October 4 to Noon, Tuesday, October 7, 2008 at the Hilton Hotel and Conference Center, Eugene, Oregon. More info |
Discussion Forum |
FA Research Labs
- add your lab link! Join OWW
- Lab Wiki Tutorial
- Hoatlin Lab, Oregon Health and Science University
Getting Started with wiki and OWW
Useful links for FA research
Pub Med FA literature
Fanconi Anemia Research Fund (FARF)
Request research materials from FARF
Request research materials from the Hoatlin Lab
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4 June 2023
m 07:44 | User:Richard J. Abbott diffhist +8 Richard J. Abbott talk contribs (→Publications) |
3 June 2023
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1 June 2023
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17:46 | BioMicroCenter:Pricing diffhist −79 Stuart S. Levine talk contribs (→SHORT READ LIBRARY - RNA) |
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09:06 | UA Biophysics:Protocols:Carotenoid Extration ESP 5 changes history +2,390 [Elizabeth Suesca (5×)] | |||
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08:43 (cur | prev) +781 Elizabeth Suesca talk contribs (→Procedimiento) | ||||
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08:25 (cur | prev) +1,023 Elizabeth Suesca talk contribs (→Materiales para 6 gramos de célula) |
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08:25 Elizabeth Suesca talk contribs uploaded File:Acetato.png |
31 May 2023
N 14:39 | 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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14:24 | UA Biophysics:Protocols:K2HPO4 KH2PO4 Buffer diffhist +54 Elizabeth Suesca talk contribs |
14:23 | UA Biophysics:Protocols diffhist −7 Elizabeth Suesca talk contribs (→BUFFERS) |
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N 14:22 | UA Biophysics:Protocols:Elution Buffer 2 changes history +1,055 [Elizabeth Suesca (2×)] | |||
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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 14:03 | UA Biophysics:Protocols:Calcein ESP 3 changes history +1,249 [Elizabeth Suesca (3×)] | |||
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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...") |
12:48 | BioMicroCenter:QC diffhist −421 Stuart S. Levine talk contribs (→AGILENT BIOANALYZER 2100) |
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08:33 (cur | prev) −804 Elizabeth Suesca talk contribs (Replaced content with " Calcein_ESP<br>") Tag: Replaced |
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08:32 | UA Biophysics:Protocols:Bacteria for Lipid Extraction 4 changes history −1,049 [Elizabeth Suesca (4×)] | |||
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N 08:31 | 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...") |
06:42 | UA Biophysics:Protocols:Lipid Extraction diffhist −9 Elizabeth Suesca talk contribs |
30 May 2023
23:52 | Hexlab diffhist +440 Ximiao He talk contribs |
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