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       <li><span class="spantitle2">Biosafety level: </span> de ouf.</li>

      <li><span class="spantitle2">Gros caca: </span> precautions and containment rules for safely working with biological agents in laboratory facilities.</li>

       <li><span class="spantitle2">Cloning: </span>recombinant DNA molecules inserted into a plasmid or virus "vector." The vector must then be introduced into a host cell without killing it.</li>

      <li><span class="spantitle2">Device: </span>an engineered genetic object that produces a human-defined function under specified conditions. Devices are produced by combining one or more standard biological parts.</li>

       <li><span class="spantitle2">Gel electrophoresis: </span>the use of current to draw a polymer (like DNA or proteins) through a sieving matrix, separating the polymers by size. Most often agarose is the matrix used for DNA electrophoresis, and polyacrylamide is the matrix used for proteins.</li>

       <li><span class="spantitle2">iGEM: </span> the international Genetically Engineered Machine competition in which teams of undergraduates build living systems from standardized, biological parts.</li>

       <li><span class="spantitle2">Part: </span>a nucleic acid-encoded biological function.</li>

       <li><span class="spantitle2">PCR: </span>a technique for amplifying DNA of known or unknown sequence. The reactions require only 4 components: DNA to be amplified, oligonucleotide primers to bind sequences flanking the target, dNTPs to polymerize into new DNA chains, and a heat stable polymerase in a buffered solution to carry out the synthesis reaction.</li>

       <li><span class="spantitle2">Plasmid: </span>a circular, double-stranded DNA molecule typically containing a few thousand base pairs that replicates within a cell independently of the chromosomal DNA. Plasmid DNA is easily purified from cells, manipulated using common lab techniques and incorporated into cells.</li>

       <li><span class="spantitle2">Promoter: </span>sequence of DNA to which RNA polymerase binds for initiation of transcription.</li>

       <li><span class="spantitle2">Recombinase: </span>Recombinases are genetic recombination enzymes. DNA recombinases are widely used in multicellular organisms to manipulate the structure of genomes, and to control gene expression. These enzymes, derived from bacteria and fungi, catalyze directionally sensitive DNA exchange reactions between short (30–40 nucleotides) target site sequences that are specific to each recombinase. These reactions enable four basic functional modules, excision/insertion, inversion, translocation and cassette exchange, which have been used individually or combined in a wide range of configurations to control gene expression.</li>

       <li><span class="spantitle2">Riboswitch: </span>Riboswitch is a regulatory segment of a messenger RNA molecule that binds a small molecule, resulting in a change in production of the proteins encoded by the mRNA. Thus, an mRNA that contains a riboswitch is directly involved in regulating its own activity, in response to the concentrations of its effector molecule. The discovery that modern organisms use RNA to bind small molecules, and discriminate against closely related analogs, expanded the known natural capabilities of RNA beyond its ability to code for proteins, catalyze reactions, or to bind other RNA or protein macromolecules.</li>

       <li><span class="spantitle2">Standardization: </span>a series of assembly and characterization rules. In time, these standards may allow the reliable physical and functional assembly of genetic parts into devices, and devices into systems.</li>

       <li><span class="spantitle2">Transcription: </span> the reaction that converts of DNA-templated information to RNA. This reaction is catalyzed by one of several RNA polymerases.</li>

       <li><span class="spantitle2">Transcriptional Terminator: </span>a sequence of DNA that signals the RNA polymerase to cease the synthesis of RNA. Terminator sequences are often inverted repeats in the DNA that fold into stem-loop structures, leading the RNA polymerase to pause and leave the DNA it is transcribing.</li>

       <li><span class="spantitle2">Translation: </span> the reaction that converts RNA-templated information to protein. This reaction is catalyzed by ribosomes.</li>