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See iGEM:Help for useful help pages for iGEM teams! Please add to the list.

2009

OpenWetWare:IGEM Teams/2009

2008

Brown University
Caltech
Cambridge
Chiba University
Harvard
HKUSTers
Imperial College London
Johns Hopkins University
Kyoto University
Melbourne
Mexico UNAM-IPN
Michigan
MIT
National Yang Ming University
Nanyang Technological University
Newcastle University
Peking University
Penn State
Purdue
TU Delft
UC Berkeley
University of Hawaii
University of Warsaw
University of Washington
Valencia
Virginia
Tsinghua
Cornell University

2007

Brown University
Caltech
Harvard
Imperial
MIT
NYMU
Peking
Penn State
Tianjin University
Tsinghua
Turkey
Virginia
UCSF
Davidson/Missouri Western State University

2006

UC Berkeley
MIT
Harvard
Penn State
Imperial

iGEM is the international genetically engineered machines competition. The objective of the competition is to design and build an engineered biological system using DNA. Systems will be constructed from standard biological parts. You can read more about last year's competition here.

Useful pages for inter-team collaboration

Good Lab Citizenship

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Wiki tips

  1. To easily add a link to a part's Registry page, use the <bbpart></bbpart> tags. For instance, <bbpart>BBa_R0011</bbpart> gives <bbpart>BBa_R0011</bbpart>.

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History

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2 May 2024

     14:21  Biophysics Lab:Reprints‎‎ 4 changes history +539 [Elizabeth Suesca‎ (4×)]
     
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14:20 (cur | prev) +140 Elizabeth Suesca talk contribs
     
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12:54 (cur | prev) +78 Elizabeth Suesca talk contribs
     14:04  UA Biophysics:Protocols‎‎ 5 changes history +1,141 [Elizabeth Suesca‎ (5×)]
     
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14:03 (cur | prev) +316 Elizabeth Suesca talk contribs
     
13:17 (cur | prev) +848 Elizabeth Suesca talk contribs
     
08:13 (cur | prev) +65 Elizabeth Suesca talk contribs (→‎BUFFERS)
     
08:07 (cur | prev) −42 Elizabeth Suesca talk contribs
     14:04  UA Biophysics:Microscopes‎‎ 3 changes history +818 [Elizabeth Suesca‎ (3×)]
     
14:04 (cur | prev) −44 Elizabeth Suesca talk contribs
     
13:12 (cur | prev) +864 Elizabeth Suesca talk contribs
     
09:34 (cur | prev) −2 Elizabeth Suesca talk contribs
     14:04  UA Biophysics:Equipment‎‎ 2 changes history +34 [Elizabeth Suesca‎ (2×)]
     
14:04 (cur | prev) −44 Elizabeth Suesca talk contribs
     
12:54 (cur | prev) +78 Elizabeth Suesca talk contribs
     13:19  BioMicroCenter:Covaris‎‎ 8 changes history −69 [Noelani Kamelamela‎ (8×)]
     
13:19 (cur | prev) +2 Noelani Kamelamela talk contribs
     
13:18 (cur | prev) −74 Noelani Kamelamela talk contribs
     
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13:15 (cur | prev) −3 Noelani Kamelamela talk contribs (→‎E220 Evolution)
     
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12:57 (cur | prev) +4 Noelani Kamelamela talk contribs
     12:55  Biophysics Lab:Contact diffhist +78 Elizabeth Suesca talk contribs
     12:53  Biophysics Lab:Lab Members‎‎ 3 changes history +1,050 [Elizabeth Suesca‎ (3×)]
     
12:53 (cur | prev) +77 Elizabeth Suesca talk contribs
     
12:50 (cur | prev) +3 Elizabeth Suesca talk contribs
     
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     12:52  Biophysics diffhist +78 Elizabeth Suesca talk contribs
     12:44  Biophysics Lab:In the lab‎‎ 3 changes history +78 [Elizabeth Suesca‎ (3×)]
     
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09:35 (cur | prev) −9 Elizabeth Suesca talk contribs
     
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     09:23  UA Biophysics:Protocols:Lipid Extration ESP diffhist +53 Elizabeth Suesca talk contribs
N    08:19  UA Biophysics:Protocols:Buffer HEPES diffhist +689 Elizabeth Suesca talk contribs (Created page with "'''Buffer HEPES: 500 mL, pH 7.4 ''' '''Este buffer no puede ser usado para trabajar con Calceina, en ese caso es obligatorio usar un buffer de elución.''' ==Materiales== * HEPES 2,383 g * NaCl 3,1896 g * NaOH 1 M * HCl 1 M ==Procedimiento== # Colocar 400 ml de agua deionizada en la botella con agitador. # Diluir el HEPES y el NaCl # Ajustar pH a 7.4 usando NaOH y/o HCl. # Sacar el agitador y completar los 500 mL con agua deionizada {| class="wikitable" style="...")
N    08:04  UA Biophysics:Protocols:Elution Buffer8 mOsM ESP‎‎ 2 changes history +1,010 [Elizabeth Suesca‎ (2×)]
     
08:04 (cur | prev) +43 Elizabeth Suesca talk contribs
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07:53 (cur | prev) +967 Elizabeth Suesca talk contribs (Created page with " ==Materiales== * HEPES 9.532 g * NaCl * NaOH 1 M 30 ml * HCl 1 M ==Procedimiento== # Colocar 1.8 litros de agua deionizada en la botella con un agitador. # Diluir el HEPES (concentracion final de 20 mM) y el NaCl (concnetracion final de 170 mM). # Ajustar pH a 7.4 usando NaOH y/o HCl (Generalmente se inicia con pH de 5.4) # Determinar la concentración de HCl y NaOH. Por ejemplo, si entre los dos se agregaron 16 ml a 1M, entonces para un buffer de 2 L la concentrac...")
     07:54  UA Biophysics:Protocols:Elution Buffer ESP‎‎ 2 changes history +70 [Elizabeth Suesca‎ (2×)]
     
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     07:44  UA Biophysics:Protocols:Elution Buffer diffhist −27 Elizabeth Suesca talk contribs
     07:42  UA Biophysics:Protocols:Calcein ESP‎‎ 2 changes history +38 [Elizabeth Suesca‎ (2×)]
     
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     07:36  UA Biophysics:Protocols:Calcein8 ESP‎‎ 2 changes history +5 [Elizabeth Suesca‎ (2×)]
     
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     06:08  Beauchamp:Publications diffhist +47 Michael S Beauchamp talk contribs (→‎Peer-reviewed journal articles)

1 May 2024

     19:35  Beauchamp:Publications diffhist +88 Michael S Beauchamp talk contribs (→‎Peer-reviewed journal articles)
     19:18  Microfluidic Vasculature for Cell Culture - Lilin Zhao, Melissa Deschamps, Marissa Burgess, Matthew Tiller, Jacob Kellett, Tina Leong, Katelyn Mullen, Daniel Bell, Anna Comperchio, Evelyn Moore‎‎ 7 changes history −5 [Ejmoore‎ (7×)]
     
19:18 (cur | prev) 0 Ejmoore talk contribs (→‎Applications for Understanding Tumor Metastasis)
     
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19:17 (cur | prev) 0 Ejmoore talk contribs (→‎Mimicking Geometry of Blood Vessels)
     
19:17 (cur | prev) −1 Ejmoore talk contribs (→‎Mimicking Geometry of Blood Vessels)
     
19:16 (cur | prev) −2 Ejmoore talk contribs (→‎Introduction)
     
19:16 (cur | prev) +1 Ejmoore talk contribs (→‎Introduction)
     
19:16 (cur | prev) −1 Ejmoore talk contribs (→‎Applications for Understanding Tumor Metastasis)

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