Difference between revisions of "Team:BGU Israel/Notebook"

 
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           <h1 class="animated fadeInUp">Notebook</h1>
 
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<h1>February</h1>
 
<h1>February</h1>
 
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<p>In this example we have added a "plus" sign to each button. When the user clicks on the button, the "plus" sign is replaced with a "minus" sign.</p>
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<p>We began working in our brand-new lab space! When we first arrived, the lab was nothing but two work benches. We had to collect and organize the equipment, materials, cell culture room, and work area; all according to lab safety standards.  We also began cloning the plasmids for our experiments and learning how to work with cell culture by practicing on HEK293 cells.<br/>
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<button class="accordion">Week1 (2.2.2018 - 8.2.2018)</button>
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<br/>
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<b>Highlights:</b> clone Steap4, Timp1, F4/80 into pGL4.17 and pGL3 plasmid for Promoter Assay.
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</p>
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<button class="accordion">Week 1</button>
 
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<object data="https://static.igem.org/mediawiki/2018/a/a6/T--BGU_Israel--notebook_week1.pdf" width="100%" height="500">
 
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<button class="accordion">Week 2 (11.2.2018 - 17.2.2018)</button>
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<button class="accordion">Week 2 </button>
 
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<object data="https://static.igem.org/mediawiki/2018/f/f6/T--BGU_Israel--notebook_week2.pdf" width="100%" height="500">
 
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<button class="accordion">Week 3 (18.2.2018 - 24.2.2018)</button>
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<button class="accordion">Week 3 </button>
 
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<button class="accordion">Week 4 (25.2.2018 - 3.3.2018)</button>
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<button class="accordion">Week 4</button>
 
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<object data="https://static.igem.org/mediawiki/2018/3/36/T--BGU_Israel--notebook_week4.pdf" width="100%" height="500">
 
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<h1>March</h1>
 
<h1>March</h1>
 
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<p>In this example we have added a "plus" sign to each button. When the user clicks on the button, the "plus" sign is replaced with a "minus" sign.</p>
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<p>
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<button class="accordion">Week 5 (4.3.2018 - 10.3.2018)</button>
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In March, we experienced our first little success. We cloned our promoters into the pGL3 vector and were able to begin our first experiment, the Promoter Assay. Meanwhile, so far, our practice cells were alive and well.
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<br/>
 +
<br/>
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<b>Highlights:</b> A decision was made to concentrate our efforts on the pGL3 plasmid expression assay. Because, then we could compare the expression among the promoters and we wouldn’t have to use two sets of luciferase kits.
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</p>
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<button class="accordion">Week 5</button>
 
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<object data="https://static.igem.org/mediawiki/2018/8/83/T--BGU_Israel--notebook_week5.pdf" width="100%" height="500">
 
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</div>
 
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<button class="accordion">Week 6 (11.3.2018 - 17.3.2018)</button>
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<button class="accordion">Week 6</button>
 
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<object data="https://static.igem.org/mediawiki/2018/1/10/T--BGU_Israel--notebook_week6.pdf" width="100%" height="500">
 
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</div>
 
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<button class="accordion">Week 7 (18.3.2018 - 24.3.2018)</button>
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<button class="accordion">Week 7</button>
 
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<object data="https://static.igem.org/mediawiki/2018/9/97/T--BGU_Israel--notebook_week7.pdf" width="100%" height="500">
 
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<button class="accordion">Week 8 (25.3.2018 - 31.3.2018)</button>
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<button class="accordion">Week 8</button>
 
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<object data="https://static.igem.org/mediawiki/2018/d/de/T--BGU_Israel--notebook_week8.pdf" width="100%" height="500">
 
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<h1>April</h1>
 
<h1>April</h1>
 
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<p>In this example we have added a "plus" sign to each button. When the user clicks on the button, the "plus" sign is replaced with a "minus" sign.</p>
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<p>
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<button class="accordion">Week 9 (1.4.2018 -7.4.2018)</button>
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Our long-awaited microglia and astrocytes arrived! While our cell lines were getting used to their new home, we began cloning our crisper and gRNA plasmids for our two-component system.
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<br/>
 +
<br/>
 +
<b>Highlights:</b> Received microglia and astrocytes cell lines, px601, H1, H2 CMV-dCas9-VPR, building plasmids with Gibson assembly.
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</p>
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<button class="accordion">Week 9</button>
 
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<button class="accordion">Week 10 (8.4.2018 -14.4.2018)</button>
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<button class="accordion">Week 11 (15.4.2018 -21.4.2018)</button>
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<object data="https://static.igem.org/mediawiki/2018/7/78/T--BGU_Israel--notebook_week11.pdf" width="100%" height="500">
 
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<button class="accordion">Week 12 (22.4.2018 -30.4.2018)</button>
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<object data="https://static.igem.org/mediawiki/2018/d/db/T--BGU_Israel--notebook_week12.pdf" width="100%" height="500">
 
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<h1>May</h1>
 
<h1>May</h1>
 
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<p>In this example we have added a "plus" sign to each button. When the user clicks on the button, the "plus" sign is replaced with a "minus" sign.</p>
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<p>
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<button class="accordion">Week 13 (6.5.2018 - 12.5.2018)</button>
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After a tireless journey, we successfully cloned most of our system’s plasmids. Now we began attempts to transfect these plasmids into our cell lines with different transfection reagents. Additionally, we began the promoter assay and astrocyte reactivity assay.
 +
<br/>
 +
<br/>
 +
<b>Highlights:</b> Began Promoter assay, transfection attempts with reagents, ELISA for astrocyte reactivity assay.
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</p>
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<button class="accordion">Week 13</button>
 
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<object data="https://static.igem.org/mediawiki/2018/3/34/T--BGU_Israel--notebook_week13.pdf" width="100%" height="500">
 
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<button class="accordion">Week 14 (13.5.2018 - 19.5.2018)</button>
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<button class="accordion">Week 14</button>
 
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<button class="accordion">Week 15 (20.5.2018 - 26.5.2018)</button>
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<button class="accordion">Week 15</button>
 
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<button class="accordion">Week 16 (27.5.2018 - 31.5.2018)</button>
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<button class="accordion">Week 16</button>
 
<div class="panel2">
 
<div class="panel2">
 
<object data="https://static.igem.org/mediawiki/2018/2/2d/T--BGU_Israel--notebook_week16.pdf" width="100%" height="500">
 
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<h1>June</h1>
 
<h1>June</h1>
 
<div class="col-sm-8 col-sm-offset-2">
 
<div class="col-sm-8 col-sm-offset-2">
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<p>In this example we have added a "plus" sign to each button. When the user clicks on the button, the "plus" sign is replaced with a "minus" sign.</p>
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<p>
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<button class="accordion">Week 17 (1.6.2018 - 9.6.2018)</button>
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In June we had to face the music; our transfection was not working. We began exploring alternatives ways to insert our plasmids into our cells, such as electroporation, calcium phosphate transfection, and additional transfection reagents.
 +
<br/>
 +
<br/>
 +
<b>Highlights:</b> Astrocyte Western blot, Electroporation of microglia.
 +
</p>
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<button class="accordion">Week 17</button>
 
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<object data="https://static.igem.org/mediawiki/2018/6/6e/T--BGU_Israel--notebook_week17.pdf" width="100%" height="500">
 
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<button class="accordion">Week 18 (10.6.2018 - 16.6.2018)</button>
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<button class="accordion">Week 18</button>
 
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<object data="https://static.igem.org/mediawiki/2018/7/7c/T--BGU_Israel--notebook_week18.pdf" width="100%" height="500">
 
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<button class="accordion">Week 19 (17.6.2018 - 23.6.2018)</button>
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<button class="accordion">Week 19</button>
 
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<div class="panel2">
 
<object data="https://static.igem.org/mediawiki/2018/2/22/T--BGU_Israel--notebook_week19.pdf" width="100%" height="500">
 
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<button class="accordion">Week 20 (24.6.2018 - 30.6.2018)</button>
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<button class="accordion">Week 20</button>
 
<div class="panel2">
 
<div class="panel2">
 
<object data="https://static.igem.org/mediawiki/2018/7/79/T--BGU_Israel--notebook_week20.pdf" width="100%" height="500">
 
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<h1>July</h1>
 
<h1>July</h1>
 
<div class="col-sm-8 col-sm-offset-2">
 
<div class="col-sm-8 col-sm-offset-2">
−
<p>In this example we have added a "plus" sign to each button. When the user clicks on the button, the "plus" sign is replaced with a "minus" sign.</p>
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<p>
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<button class="accordion">Week 21 ( 1.7.2018 - 7.7.2018)</button>
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In July we preformed further attempts to transfect our cells and reactivity assays, and let’s not forget exams period.
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<br/>
 +
<br/>
 +
<b>Highlights:</b> Electroporation of microglia, mycoplasma assay, colony PCR after the microglia electroporation, transfection attempts with reagents, astrocyte reactivity assay using western blot.
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</p>
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<button class="accordion">Week 21</button>
 
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<div class="panel2">
 
<object data="https://static.igem.org/mediawiki/2018/4/47/T--BGU_Israel--notebook_week21.pdf" width="100%" height="500">
 
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<button class="accordion">Week 22 (8.7.2018 - 14.7.2018)</button>
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<button class="accordion">Week 22</button>
 
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<div class="panel2">
 
<object data="https://static.igem.org/mediawiki/2018/d/db/T--BGU_Israel--notebook_week22.pdf" width="100%" height="500">
 
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<button class="accordion">Week 23 (15.7.2018 - 21.7.2018)</button>
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<button class="accordion">Week 23</button>
 
<div class="panel2">
 
<div class="panel2">
 
<object data="https://static.igem.org/mediawiki/2018/8/89/T--BGU_Israel--notebook_week23.pdf" width="100%" height="500">
 
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<button class="accordion">Week 24 (22.7.2018 - 31.7.2018)</button>
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<button class="accordion">Week 24</button>
 
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<div class="panel2">
 
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<h1>August</h1>
 
<h1>August</h1>
 
<div class="col-sm-8 col-sm-offset-2">
 
<div class="col-sm-8 col-sm-offset-2">
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<p>In this example we have added a "plus" sign to each button. When the user clicks on the button, the "plus" sign is replaced with a "minus" sign.</p>
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<p>
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<button class="accordion">Week 25 (1.8.2018 - 11.8.2018)</button>
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The summer was in full swing and with it our iGEM team. Each team member worked full force on experiments to reach a proof of concept.
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<br/>
 +
<br/>
 +
<b>Highlights:</b> continued reactive astrocyte experiments.
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</p>
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<button class="accordion">Week 25</button>
 
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<button class="accordion">Week 26 (12.8.2018 - 18.8.2018)</button>
 
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<button class="accordion">Week 27 (19.8.2018 - 25.8.2018)</button>
 
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<button class="accordion">Week 28 (26.8.2018 - 31.8.2018)</button>
 
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<h1>Experiments</h1>
 
<h1>Experiments</h1>
 
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<div class="col-sm-8 col-sm-offset-2">
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<p>In this example we have added a "plus" sign to each button. When the user clicks on the button, the "plus" sign is replaced with a "minus" sign.</p>
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<button class="accordion">Calcium Phosphate Transfection</button>
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<button class="accordion">Exp1 (4.3.2018 - 10.3.2018)</button>
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                         <embed src="https://static.igem.org/mediawiki/2018/3/34/T--BGU_Israel--notebook_exp_calcium_phosphate.pdf" type="application/pdf" width="100%" height="600" />
 
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<button class="accordion">Exp2</button>
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<button class="accordion">Cytokine Inhibition</button>
 
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                         <embed src="https://static.igem.org/mediawiki/2018/3/36/T--BGU_Israel--notebook_week4.pdf" type="application/pdf" width="100%" height="600" />
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                         <embed src="https://static.igem.org/mediawiki/2018/d/da/T--BGU_Israel--notebook_exp_qpcr.pdf" type="application/pdf" width="100%" height="600" />
 
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<button class="accordion">Exp3</button>
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Latest revision as of 16:34, 17 October 2018

OriginALS

OriginALS

Notebook

February March April May
June July August Experiments

February

We began working in our brand-new lab space! When we first arrived, the lab was nothing but two work benches. We had to collect and organize the equipment, materials, cell culture room, and work area; all according to lab safety standards. We also began cloning the plasmids for our experiments and learning how to work with cell culture by practicing on HEK293 cells.

Highlights: clone Steap4, Timp1, F4/80 into pGL4.17 and pGL3 plasmid for Promoter Assay.

March

In March, we experienced our first little success. We cloned our promoters into the pGL3 vector and were able to begin our first experiment, the Promoter Assay. Meanwhile, so far, our practice cells were alive and well.

Highlights: A decision was made to concentrate our efforts on the pGL3 plasmid expression assay. Because, then we could compare the expression among the promoters and we wouldn’t have to use two sets of luciferase kits.

April

Our long-awaited microglia and astrocytes arrived! While our cell lines were getting used to their new home, we began cloning our crisper and gRNA plasmids for our two-component system.

Highlights: Received microglia and astrocytes cell lines, px601, H1, H2 CMV-dCas9-VPR, building plasmids with Gibson assembly.

May

After a tireless journey, we successfully cloned most of our system’s plasmids. Now we began attempts to transfect these plasmids into our cell lines with different transfection reagents. Additionally, we began the promoter assay and astrocyte reactivity assay.

Highlights: Began Promoter assay, transfection attempts with reagents, ELISA for astrocyte reactivity assay.

June

In June we had to face the music; our transfection was not working. We began exploring alternatives ways to insert our plasmids into our cells, such as electroporation, calcium phosphate transfection, and additional transfection reagents.

Highlights: Astrocyte Western blot, Electroporation of microglia.

July

In July we preformed further attempts to transfect our cells and reactivity assays, and let’s not forget exams period.

Highlights: Electroporation of microglia, mycoplasma assay, colony PCR after the microglia electroporation, transfection attempts with reagents, astrocyte reactivity assay using western blot.

August

The summer was in full swing and with it our iGEM team. Each team member worked full force on experiments to reach a proof of concept.

Highlights: continued reactive astrocyte experiments.

Experiments

OriginALS

About Us


The BGU-iGEM team “OriginALS” hopes to develop an innovative therapeutic approach to prolong the life expectancy of ALS patients, using Synthetic Biology. We are dedicated to promoting ALS awareness and research in Israel through public engagement and educational activities.

    Keep in Touch

  • @iGEMBGU
  • @igem_2018_bgu
  • @originalsbgu
  • originalsbgu@gmail.com

    Address

  • Ben-Gurion University of the Negev
    Ben Gurion 1, Beer Sheva 8410501, Israel