User:Ricardo Vidal/sandbox

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Tables

  • By simplye adding {{table}} to your tables, you achieve a nice thin grey border on your tables
{|{{table}} width="400px"
|+ Table 1 - This is a nice simple outlined table.
! style="background-color:#EEE;"|name !! style="background-color:#EEE;"|number
|-
| John || 2
|-
| Jill || 3
|-
| Jack || 4
|-
| Joseph || 5
|-
| Jenny || 6
|}
Table 1 - This is a nice simple outlined table.
name number
John 2
Jill 3
Jack 4
Joseph 5
Jenny 6

Playground

DPL



Recent Changes

List of abbreviations:
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26 July 2024

     14:07  UA Biophysics:Equipment‎‎ 3 changes history +48 [Elizabeth Suesca‎ (3×)]
     
14:07 (cur | prev) −6 Elizabeth Suesca talk contribs
     
14:06 (cur | prev) −5 Elizabeth Suesca talk contribs
     
12:32 (cur | prev) +59 Elizabeth Suesca talk contribs
     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
N    12:42  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  UA Biophysics: Lyophilizer diffhist +17 Elizabeth Suesca talk contribs
N    09:33  UA Biophysics:Protocols:YPD 1L‎‎ 2 changes history +486 [Elizabeth Suesca‎ (2×)]
     
09:33 (cur | prev) +363 Elizabeth Suesca talk contribs
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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×)]
     
09:30 (cur | prev) +1 Elizabeth Suesca talk contribs
     
09:29 (cur | prev) +8 Elizabeth Suesca talk contribs
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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×)]
     
09:18 (cur | prev) +53 Elizabeth Suesca talk contribs (→‎MEDIA)
     
08:24 (cur | prev) +22 Elizabeth Suesca talk contribs
     
08:22 (cur | prev) +48 Elizabeth Suesca talk contribs (→‎VESICLES)
N    09:14  UA Biophysics:Protocols:Glass Cleaning ESP‎‎ 2 changes history +1,259 [Elizabeth Suesca‎ (2×)]
     
09:14 (cur | prev) −9 Elizabeth Suesca talk contribs
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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×)]
     
09:13 (cur | prev) +511 Elizabeth Suesca talk contribs
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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

24 July 2024

23 July 2024

     19:16  Hu:Publications‎‎ 2 changes history −4 [Hugangqing‎ (2×)]
     
19:16 (cur | prev) −12 Hugangqing talk contribs
     
18:57 (cur | prev) +8 Hugangqing talk contribs
     18:56  Hu diffhist +19 Hugangqing talk contribs