NYMU Taipei/Protocols2
From 2007.igem.org
(Difference between revisions)
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<li><font size="2">Quantitation of Nucleic acid concentration</font> | <li><font size="2">Quantitation of Nucleic acid concentration</font> | ||
<ul> | <ul> | ||
- | <li><font size="2"> | + | <li><font size="2">[[http://en.wikipedia.org/wiki/Quantification_of_nucleic_acids">Wikipedia]]</font></li> |
- | <li><font size="2"> | + | <li><font size="2">[[http://www.piercenet.com/Objects/View.cfm?type=Page&ID=0A0A7BB1-7582-4611-A116-6F583EC01666">Pierce]]</font></li> |
- | <li><font size="2"> | + | <li><font size="2">[[http://mcbl.iisc.ernet.in/Welcome%20to%20MCBL/Faculty/Parag/microarray%20workshop%20details/quantitation.html">India]]</font></li> |
- | <li><font size="2"> | + | <li><font size="2">[[http://www.kreatech.com/pages/Focus-Areas/*-Hybridization-___-Labeling-protocols/Small-RNA-Labeling-protocol/">Kreatech Biotechnology]] </font></li> |
</ul> | </ul> | ||
</li> | </li> | ||
- | <li><font face="Arial" size="2"><span lang="EN-US" style="font-size: 9.5pt; font-family: Arial"> | + | <li><font face="Arial" size="2"><span lang="EN-US" style="font-size: 9.5pt; font-family: Arial">[[http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/setting_up_reaction.asp">Setting Up a Restriction Endonuclease Reaction]]</span></font><font size="2"> </font></li> |
<li><font size="2">DNA Analysis through Gel Electrophoresis</font></li> | <li><font size="2">DNA Analysis through Gel Electrophoresis</font></li> | ||
<li><font size="2">Ligate blunt or cohesive ends in 5 minutes at room temperature</font> | <li><font size="2">Ligate blunt or cohesive ends in 5 minutes at room temperature</font> | ||
<ul> | <ul> | ||
- | <li><font size="2"> | + | <li><font size="2">[[http://www.neb.com/nebecomm/products/productM2200.asp">Quick Ligation Kit (NEB)]]</font></li> |
- | <li><font size="2"> | + | <li><font size="2">[[http://www.ubi.ca/cart/index.php/cPath/27_163_165">Fast Ligation Kit (UBI)]]</font></li> |
- | <li><font size="2"> | + | <li><font size="2">[[http://www.epibio.com/item.asp?ID=296">Fast-Link DNA Ligation Kit (EPICENTRE Biotechnologies)]]</font></li> |
- | <li><font size="2"> | + | <li><font size="2">[[http://www.fermentas.com/catalog/kits/kitrapidligation.htm">Rapid Ligation Kit (Fermentas)]]</font></li> |
<li><font size="2">All of these are just normal ligase buffers with PEG8000 at a 10-12% concentration. The NEB catalogue gives the original reference. <br /> | <li><font size="2">All of these are just normal ligase buffers with PEG8000 at a 10-12% concentration. The NEB catalogue gives the original reference. <br /> | ||
Use of crowding agents like PEG allow 5-minute sticky end ligations.</font></li> | Use of crowding agents like PEG allow 5-minute sticky end ligations.</font></li> | ||
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<li><font size="2">Vector sequences </font> | <li><font size="2">Vector sequences </font> | ||
<ul> | <ul> | ||
- | <li> | + | <li>[[http://seq.yeastgenome.org/vectordb/"><font size="2">VectorDB - Molecular Biology Vector Sequence Database</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.shigen.nig.ac.jp/cvector/cvector.html"><font size="2">The cloning vector collection</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/dna_sequences_maps.asp"><font size="2">New England Biolabs (NEB) DNA Sequences and Maps</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.promega.com/vectors/cloning_vectors.htm"><font size="2">Promega Cloning Vectors</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.emdbiosciences.com/Products/BrowseProductsByCategory.asp?catid=1628"><font size="2">Novagen Vector Maps</font>]]<font size="2"> </font></li> |
</ul> | </ul> | ||
</li> | </li> | ||
- | <li> | + | <li>[[http://wishart.biology.ualberta.ca/PlasMapper/"><font size="2">PlasMapper Version 2.0 - automatically generates and annotates plasmid maps</font>]]<font size="2"> </font></li> |
</ul> | </ul> | ||
</li> | </li> | ||
<li><font size="2">[[Transformation]] </font></li> | <li><font size="2">[[Transformation]] </font></li> | ||
<li><font size="2">[[Production of heterologous proteins in Escherichia coli]] </font></li> | <li><font size="2">[[Production of heterologous proteins in Escherichia coli]] </font></li> | ||
- | <li> | + | <li>[[http://openwetware.org/wiki/Endy:Preparing_Antibiotic_Stocks"><font size="2">Antibiotics</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://openwetware.org/wiki/Synthetic_Biology:BioBricks/Part_fabrication"><font face="Arial" size="2">Part fabrication</font>]]<font size="2"> (</font>[[http://openwetware.org/wiki/Enzyme_selection_for_BioBricks_digest"><font size="2">Enzyme selection for BioBricks digest</font>]]<font size="2">!!) </font></li> |
- | <li> | + | <li>[[http://openwetware.org/wiki/BioBricks_construction_tutorial"><font size="2">BioBricks construction tutorial</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://openwetware.org/wiki/Silver:_BB_Strategy"><font size="2">Fusion protein</font>]]<font size="2"> </font></li> |
<li><font size="2">Glucose assay </font> | <li><font size="2">Glucose assay </font> | ||
<ul> | <ul> | ||
- | <li><font color="#000000" size="2"> | + | <li><font color="#000000" size="2">[[http://en.wikipedia.org/wiki/Blood_sugar">Blood sugar (from Wikipedia)]]</font><font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.genengnews.com/articles/chtitem.aspx?tid=1624&chid=3"><font size="2">Glucose Measurement for Cell Culture</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.sigmaaldrich.com/Area_of_Interest/Life_Science/Metabolomics/Product_Highlights/Enzymatic_Kits.html"><font size="2">Glucose Assay Kits from SigmaAldrich</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.bioassaysys.com/Order.html"><font size="2">Glucose Assay Kit from QuantiChrom</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.rpbiotech.com/Biochem_diag_kits/Glucose_Diagnostic_Kit.htm"><font size="2">Biochemical glucose kit from rpbiotech</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.anilinepharma.com/products.php?catg=ds&id=1"><font size="2">Glucose Meter from AnilinePharma</font>]]<font size="2"> </font></li> |
</ul> | </ul> | ||
</li> | </li> | ||
<li><font size="2">Mammalian Gene Collection (MGC) Full-length cDNA clones </font> | <li><font size="2">Mammalian Gene Collection (MGC) Full-length cDNA clones </font> | ||
<ul> | <ul> | ||
- | <li> | + | <li>[[http://mgc.nci.nih.gov/"><font size="2">at National Cancer Institute of NIH</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://genome.ym.edu.tw/libres/MGC_clones/index.htm"><font size="2">at Genome Research Center of NYMU</font>]]<font size="2"> </font></li> |
- | <li> | + | <li>[[http://www.ncbi.nlm.nih.gov/FLC/getmgc.cgi"><font size="2">NCBI MGC retrieval</font>]]<font size="2"> </font></li> |
</ul> | </ul> | ||
</li> | </li> | ||
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<h3>Dry-Lab Protocols</h3> | <h3>Dry-Lab Protocols</h3> | ||
<ul> | <ul> | ||
- | <li> | + | <li>[[http://serialbasics.free.fr/Serial_Cloner.html">serial cloner]]</li> |
<li>Protein Fusion Design | <li>Protein Fusion Design | ||
<ul> | <ul> | ||
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<ul> | <ul> | ||
<li>[[Properties of TAT Signal Peptides]]</li> | <li>[[Properties of TAT Signal Peptides]]</li> | ||
- | <li> | + | <li>[[http://www.jic.bbsrc.ac.uk/staff/tracy-palmer/signals.htm">A link to a list of Tat signal sequences provided by Tracy Palmer]]</li> |
<li>[[29 putative signal peptides]] </li> | <li>[[29 putative signal peptides]] </li> | ||
<li>[[Selected TAT signal peptides]]</li> | <li>[[Selected TAT signal peptides]]</li> | ||
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<h3>General references</h3> | <h3>General references</h3> | ||
<ul> | <ul> | ||
- | <li> | + | <li>[[http://www.neb.com/nebecomm/tech_reference/default.asp">New England Biolab (NEB) technical references]]</li> |
</ul> | </ul> | ||
[https://2007.igem.org/NYMU_Taipei/Welcome Back] | [https://2007.igem.org/NYMU_Taipei/Welcome Back] |
Revision as of 16:44, 19 October 2007
Wet-Lab Protocols
- [http://www.protocol-online.org/ Protocol online]
- PCR (7/20)
- RT-PCR
- Q-PCR
- Quantitation of Nucleic acid concentration
- [[http://en.wikipedia.org/wiki/Quantification_of_nucleic_acids">Wikipedia]]
- [[http://www.piercenet.com/Objects/View.cfm?type=Page&ID=0A0A7BB1-7582-4611-A116-6F583EC01666">Pierce]]
- [[http://mcbl.iisc.ernet.in/Welcome%20to%20MCBL/Faculty/Parag/microarray%20workshop%20details/quantitation.html">India]]
- [[http://www.kreatech.com/pages/Focus-Areas/*-Hybridization-___-Labeling-protocols/Small-RNA-Labeling-protocol/">Kreatech Biotechnology]]
- [[http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/setting_up_reaction.asp">Setting Up a Restriction Endonuclease Reaction]]
- DNA Analysis through Gel Electrophoresis
- Ligate blunt or cohesive ends in 5 minutes at room temperature
- [[http://www.neb.com/nebecomm/products/productM2200.asp">Quick Ligation Kit (NEB)]]
- [[http://www.ubi.ca/cart/index.php/cPath/27_163_165">Fast Ligation Kit (UBI)]]
- [[http://www.epibio.com/item.asp?ID=296">Fast-Link DNA Ligation Kit (EPICENTRE Biotechnologies)]]
- [[http://www.fermentas.com/catalog/kits/kitrapidligation.htm">Rapid Ligation Kit (Fermentas)]]
- All of these are just normal ligase buffers with PEG8000 at a 10-12% concentration. The NEB catalogue gives the original reference.
Use of crowding agents like PEG allow 5-minute sticky end ligations.
- Vector construction
- Vector sequences
- [[http://seq.yeastgenome.org/vectordb/">VectorDB - Molecular Biology Vector Sequence Database]]
- [[http://www.shigen.nig.ac.jp/cvector/cvector.html">The cloning vector collection]]
- [[http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/dna_sequences_maps.asp">New England Biolabs (NEB) DNA Sequences and Maps]]
- [[http://www.promega.com/vectors/cloning_vectors.htm">Promega Cloning Vectors]]
- [[http://www.emdbiosciences.com/Products/BrowseProductsByCategory.asp?catid=1628">Novagen Vector Maps]]
- [[http://wishart.biology.ualberta.ca/PlasMapper/">PlasMapper Version 2.0 - automatically generates and annotates plasmid maps]]
- Vector sequences
- Transformation
- Production of heterologous proteins in Escherichia coli
- [[http://openwetware.org/wiki/Endy:Preparing_Antibiotic_Stocks">Antibiotics]]
- [[http://openwetware.org/wiki/Synthetic_Biology:BioBricks/Part_fabrication">Part fabrication]] ([[http://openwetware.org/wiki/Enzyme_selection_for_BioBricks_digest">Enzyme selection for BioBricks digest]]!!)
- [[http://openwetware.org/wiki/BioBricks_construction_tutorial">BioBricks construction tutorial]]
- [[http://openwetware.org/wiki/Silver:_BB_Strategy">Fusion protein]]
- Glucose assay
- [[http://en.wikipedia.org/wiki/Blood_sugar">Blood sugar (from Wikipedia)]]
- [[http://www.genengnews.com/articles/chtitem.aspx?tid=1624&chid=3">Glucose Measurement for Cell Culture]]
- [[http://www.sigmaaldrich.com/Area_of_Interest/Life_Science/Metabolomics/Product_Highlights/Enzymatic_Kits.html">Glucose Assay Kits from SigmaAldrich]]
- [[http://www.bioassaysys.com/Order.html">Glucose Assay Kit from QuantiChrom]]
- [[http://www.rpbiotech.com/Biochem_diag_kits/Glucose_Diagnostic_Kit.htm">Biochemical glucose kit from rpbiotech]]
- [[http://www.anilinepharma.com/products.php?catg=ds&id=1">Glucose Meter from AnilinePharma]]
- Mammalian Gene Collection (MGC) Full-length cDNA clones
- [[http://mgc.nci.nih.gov/">at National Cancer Institute of NIH]]
- [[http://genome.ym.edu.tw/libres/MGC_clones/index.htm">at Genome Research Center of NYMU]]
- [[http://www.ncbi.nlm.nih.gov/FLC/getmgc.cgi">NCBI MGC retrieval]]
Dry-Lab Protocols
- [[http://serialbasics.free.fr/Serial_Cloner.html">serial cloner]]
- Protein Fusion Design
- rcsC-envZ cimaera design
- Twin-Arginine Translocation Pathway Signal Peptide
- Lee et al., 2006. The Bacterial Twin-Arginine Translocation Pathway. Annu. Rev. Microbiol., 60, p373-395
- Properties of TAT Signal Peptides
- [[http://www.jic.bbsrc.ac.uk/staff/tracy-palmer/signals.htm">A link to a list of Tat signal sequences provided by Tracy Palmer]]
- 29 putative signal peptides
- Selected TAT signal peptides
- Signal peptides and insulin A, B chain
- Signal peptides and IDE coding sequence
- Lee et al., 2006. The Bacterial Twin-Arginine Translocation Pathway. Annu. Rev. Microbiol., 60, p373-395
General references
- [[http://www.neb.com/nebecomm/tech_reference/default.asp">New England Biolab (NEB) technical references]]