Difference between revisions of "Team:Dundee/Part Collection"
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− | <img class="img-responsive center-block" src="./ | + | <img class="img-responsive center-block" src="https://static.igem.org/mediawiki/2015/1/17/Dundee2015characterisationBBa_K1590004.png"> |
− | <figcaption class="caption-center"> | + | <figcaption class="caption-center"><p> It was found that GFP was produced in the absence of chromate for both systems. This reason for these unexpected results could not be discerned, and further experiments are required to understand those. At this stage of the project the results indicate that ChrB might not be a repressor.</p></figcaption> |
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<img class="img-responsive center-block" src="./img/test.png"> | <img class="img-responsive center-block" src="./img/test.png"> | ||
− | <figcaption class="caption-center"> | + | <figcaption class="caption-center"><p> Successful production of GFP under the control of P<sub><i>Chr</i></sub></p></figcaption> |
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<img class="img-responsive center-block" src="./img/test.png"> | <img class="img-responsive center-block" src="./img/test.png"> | ||
− | <figcaption class="caption-center"> | + | <figcaption class="caption-center"><p> Successful production of GFP under the control of P<sub><i>Chr</i></sub></p></figcaption> |
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− | <h1>Part:BBa_K1590008 (<i> | + | <h1>Part:BBa_K1590008 (<i>LbpA</i></h1> |
<h2>Saliva Detection</h2> | <h2>Saliva Detection</h2> | ||
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<img class="img-responsive center-block" src="./img/test.png"> | <img class="img-responsive center-block" src="./img/test.png"> | ||
− | + | <figcaption class="caption-center"><p> Successful production of GFP under the control of P<sub><i>Chr</i></sub></p></figcaption> | |
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− | + | <figcaption class="caption-center"><p> Successful production of GFP under the control of P<sub><i>Chr</i></sub></p></figcaption> | |
</figure> | </figure> | ||
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<img class="img-responsive center-block" src="./img/test.png"> | <img class="img-responsive center-block" src="./img/test.png"> | ||
− | + | <figcaption class="caption-center"><p> Successful production of GFP under the control of P<sub><i>Chr</i></sub></p></figcaption> | |
</figure> | </figure> | ||
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Revision as of 02:57, 18 September 2015
Part: BBa_K1590000 (hHBA)
FluID- Blood Detection
Coding sequence for Human haemoglobin A. Haemoglobin is the tetrameric protein molecule in red blood cells that carries oxygen. It is composed of four polypeptide chains, which in adults consist of two alpha (a) globin chains and two beta (b) globin chains. In blood plasma, haptoglobin binds free haemoglobin released from red blood cells, inhibiting its oxidative activity. The haptoglobin-hemoglobin complex can then be removed by the reticuloendothelial system which is a part of the immune system. Despite this, haemoglobin is still found free in the blood plasma at a concentration of up to 0.1g/l and this is what we hope to detect. .
Part: BBa_K1590001 (hHBB)
FluID- Blood Detection
Coding sequence for Human haemoglobin B. Haemoglobin is the tetrameric protein molecule in red blood cells that carries oxygen. It is composed of four polypeptide chains, which in adults consist of two alpha (a) globin chains and two beta (b) globin chains. In blood plasma, haptoglobin binds free haemoglobin released from red blood cells, inhibiting its oxidative activity. The haptoglobin-hemoglobin complex can then be removed by the reticuloendothelial system which is a part of the immune system. Despite this, haemoglobin is still found free in the blood plasma at a concentration of up to 0.1g/l and this is what we hope to detect.
Part: BBa_K1590002 (hHBN)
FluID - Blood Detection
Coding sequence for Human haptoglobin.Haemoglobin is the tetrameric protein molecule in red blood cells that carries oxygen. It is composed of four polypeptide chains, which in adults consist of two alpha (a) globin chains and two beta (b) globin chains. In blood plasma, haptoglobin binds free haemoglobin released from red blood cells, inhibiting its oxidative activity. The haptoglobin-hemoglobin complex can then be removed by the reticuloendothelial system which is a part of the immune system. Despite this, haemoglobin is still found free in the blood plasma at a concentration of up to 0.1g/l and this is what we hope to detect.
Part: BBa_K1590003 (PChr)
Chromate Detection
Chromate responsive promoter. The promoter PChr is suspected to be inducible by chromate.
Part: BBa_K1590004 (ChrB)
Chromate Detection
Promoter sequence of chromate resistance operon of Ochrobactrum tritici 5bvl1. Regulator or Chromate responsive promoter. The protein encoded by this sequence is a putative chromate responsive repressor of PChr (BBa_K1590003).
Part:BBa_K1590006 (LSS)
Fingerprint Aging
Lanosterol Synthase catalyses the reaction from 2,3-oxido-squalene (squalene epoxide) to Lanosterol. It is one of the enzymes in the enzymatic cascade that converts squalene to cholesterol through stepwise modifications of the substrate.
Part:BBa_K1590007 (Obp2A)
Nasal Mucus Detection
Human Odorant Binding Protein 2A is a 155 amino acid (excluding the signal peptide) lipocalin of relatively low molecular weight (19318 Daltons). Structurally it forms an 8 sheet beta barrel flanked by a c-terminal alpha helix that together forms an internal hydrophobic pore known as a calix. It is secreted by the olfactory epithelial cells of the nose where it lies in high abundance within nasal mucus. Its primary function in the human body is believed to be in the transport of hydrophobic odorant proteins across the otherwise impenetrable aqueous mucus layer to the olfactory receptors of the nose. Due to its high specificity and abundance within nasal mucus, OBP2A was selected as the protein for use in nasal mucus detection.
Part:BBa_K1590008 (LbpA
Saliva Detection
Coding sequence for Lactoferrin Binding Protein A of Neisseria Meningitidis. This protein sequesters Iron for the host from Lactoferrin.
Part:BBa_K1590009 (PotD)
Semen Detection
Escherichia coli PotD sequence, encoding Spermidine/putrescine-binding periplasmic protein.
Part:BBa_K1590010 (Sbp)
Semen Detection
Murine Spermine Binding Protein Binds the carbohydrate spermine.