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Conducted a 32 cycle PCR amplification of the PCR constructs. Cleaned with the kit and nanodropped. The results were then digested with miniprepped pSB1C3 and cleaned again after a 2 hour incubation. The PCR constructs were then ligated with the digested pSB1C3 and incubated overnight.
 
Conducted a 32 cycle PCR amplification of the PCR constructs. Cleaned with the kit and nanodropped. The results were then digested with miniprepped pSB1C3 and cleaned again after a 2 hour incubation. The PCR constructs were then ligated with the digested pSB1C3 and incubated overnight.
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Revision as of 20:52, 18 September 2015

NOTEBOOK

May June July August September

Notebook

Format

Month Day, Year

Name

Protocol

Description

May 18th, 2015

Connor and Sean

Transformation

Resuspended parts BBa_E1010 and BBa_I716120 on plate 3 well 11n and plate 3 well 11m, respectively. Transformed both and placed in 37 degree incubator *Note: parts left in 37 degree incubator too long (>24 hours) and overgrew

May 21st, 2015

May 21st, 2015

Elliot and Danny

Transformation

Resuspended part BBa_K118011 on plate 3 well 20c. Transformed this part along with BBa_E1010 again.

June 3rd, 2015

Connor and Sean

Transformation

Resuspended parts BBa_K1033916 and BBa_K592009 on plate 4 well 6m and plate 1 well 15e, respectively. Transformed those parts and BBa_E1010.

*Note: BBa_K1033916 plate was thrown out due to suspicion of LBKanR mislabeling and the two other chromoproteins appear to have been switched.

Elliot and Danny

Transformation

Transformed parts BBa_E1010, BBa_K1033916, BBa_K592009, BBa_K861171 and BBa_K118011.

Will and Jerry

ZR Plasmid Miniprep Classic

Miniprepped parts BBa_K861171 and BBa_K118011. Prepared 1x TAE Buffer from stock.

June 4th, 2015

Will

Transformation

Did overall inventory and plated BBa_K861171

Connor and Sean

Liquid Cultures

Created liquid cultures of BBa_E1010 (2), BBa_K592009 (2), and BBa_K1033916 and placed in 37 degree shaking incubator overnight.

*Note: Liquid cultures spent >24 hours in 37 degree incubator, so thrown out. Also, BBa_K118011 failed to grow.

June 5th, 2015

Elliot and Danny

Liquid Cultures

Created liquid cultures of BBa_E1010 (2), BBa_K592009 (2), and BBa_K1033916 and placed in 37 degree shaking incubator overnight. LB was autoclaved and placed in 4 degree fridge.

June 6th, 2015

Elliot and Danny

ZR Plasmid Miniprep Classic

Miniprepped BBa_E1010 (2), BBa_K592009 (2), and BBa_K1033916 and nanodropped for concentrations.

June 8th, 2015

Will

Did overall inventory and made a 1L DI water stock

June 10th, 2015

Will and Jerry

PCR

Received and reconstituted MLC Parts and MLC primers. Performed PCR amplification on the MLC parts.

June 11th, 2015

Will and Jerry

Agarose Gel Electrophoresis, DNA Clean + Concentrator Prep, PCR

Ran a gel verifying the MLC parts, concentrated the PCR-generated plasmids and nanodropped. After determining that concentrations were insufficient, ran another PCR for MLC amplification. Also conducted inventory.

Connor and Sean

DNA Clean + Concentrator Prep, Transformation

Prepped the DNA and transformed BBa_J4450, which was reconstituted from plate 4 well 4b. Made a glycerol stock.

Elliot and Danny

Transformation

Created ampicillin plates and reconstituted BBa_J61100 on plate 4 well b4. Transformed BBa_J61100 on the ampicillin plates.

June 12th, 2015

Connor, Sean and Elliot

Liquid Cultures, DNA Clean and Concentrator Prep

Made 2 liquid cultures of BBa_J61100 (LBAmp) and 4 liquid cultures of BBa_J4450 (LBCam). Prepped the new MLC PCR mixes and nanodropped for concentrations.

June 13th, 2015

Elliot and Danny

ZR Plasmid Miniprep Classic

Miniprepped the liquid cultures of BBa_J61100 and BBa_J4450 (6 in total). Stored in the -20 degrees freezer.

June 14th, 2015

Elliot and Danny

Liquid Cultures

Created 3 liquid cultures of BBa_J4450 (LBCam) and 6 liquid cultures of BBa_J61100 (LBAmp).

June 15th, 2015

Connor

ZR Plasmid Miniprep Classic

Miniprepped 2 BBa_J4450 cultures and 5 BBa_J61100 cultures. Nanodropped and stored in the -20 degrees freezer.

Elliot and Danny

3A Assembly, Agarose Gel Electrophoresis

Conducted 3A Assembly with the following components: pSB1C3 (from BBa_J4450), BBa_K1033916/BBa_E1010/BBa_K592009 (downstream component) and BBa_J61100 (upstream component). Made a 1% agarose gel with the following wells: 1: 1 kb ladder; 2: BBa_E1010 #3; 3. BBa_E1010 #2; 4. BBa_K1033916 #3; 5. BBa_K592009 #2; 6. BBa_K861171 # 3; 7. 1 kb ladder. Made another 1% agarose gel: 1: 1 kb ladder; 2: 100 bp ladder; 3. BBa_K1033916 #3; 4. BBa_K592009 #2; 5. BBa_K1033916 #1; 6. BBa_K861171 #1; 7. BBa_K861171 #2; 8. BBa_K861171 #3

June 16th, 2015

Elliot + Danny + Jerry

Agarose Gel Electrophoresis

Ran a diagnostic 2% gel for the repressible.

Will + Jerry

Agarose Gel Electrophoresis

Ran a 1% gel with the following specifications: 1: 1 kb ladder; 2: 100 bp ladder; 3: BBa_K1033916 #1; 4: BBa_K1033916 #2; 5: BBa_K1033916 #3; 6: BBa_K592009 #2; 7: BBa_K861171 #1; 8: BBa_K861171 #2; 9: BBa_K861171 #3

Connor + Will

3A Assembly, Simple Recombination

Conducted a 3A assembly with the following components: pSB1C3, BBa_E1010/BBa_K592009, BBa_J1100. Conducted simple recombination (cutting a backbone and “part” with the same enzymes) with the following components: MLC1/2/3/4, pSB1C3.

Will

Transformation

Transformed the two 3A plasmids and four simple recombination plasmids.

*Note: all MLC plates failed to grow

June 17th, 2015

Will

PCR, Transformation

Conducted another PCR amplification procedure for the order MLC parts (1-4). Transformed the MLC + pSB1C3 constructs that failed to grow once more.

June 18th, 2015

Will

Agarose Gel Electrophoresis, Gel DNA Recovery Prep

Made glycerol stocks of BBa_K1033916#3/pSB1C3/BBa_J61100 (pink, so actually BBa_J4450), BBa_K592009#2/pSB1C3/BBa_J61100, BBa_E1010#2/pSB1C3/BBa_J61100. Then ran a 1% gel with the following specifications: 1: 1 kb ladder; 2: 100 bp ladder; 3: MLC1: 4: MLC2; 5: MLC3; 6: MLC4; 7: MasterMix; 8: USP H20. Then ran a DNA gel recovery prep and nanodropped. *Note: MLC remainders from the gel were not enough, so another PCR is recommended.

Connor

Zyppy Plasmid Miniprep, Transformation

Miniprepped BBa_K592009/BBa_J61100/pSB1C3 and BBa_E1010/BBa_J61100/pSB1C3 liquid cultures. Nanodropped the results. Transformed the BBa_1033916 #1/#2 3A results.

Jerry, Danny, Elliot

3A Assembly, Transformation, Agarose Gel Electrophoresis

Conducted a 3A with the following components: BBa_J4450 (pSB1C3), BBa_J61100, BBa_K1033916 #1/2. Ran a 1% digest gel with the following specifications: 1: 1 kb ladder; 2: BBa_K1033916 #1, undigested; 3: BBa_K1033916 #1, EcoRI digested; 4: BBa_K1033916 #1, SpeI digested; 5: BBa_K1033916 #1, double digest; 6: BBa_K1033916 #2, undigested; 7: BBa_K1033916 #2, EcoRI digested; 8: BBa_K1033916 #2, SpeI digested; 9: BBa_K1033916 #2, double digest; 10: BBa_K861171 #1, undigested; 11: BBa_K861171 #1, EcoRI digested; 12: BBa_K861171 #1, SpeI digested; 13: BBa_K861171 #1, double digest; 14: 100 bp ladder.

June 19th, 2015

Connor, Sean

PCR, DNA Clean + Concentration Prep, Simple Recombination, Liquid Culture

Redid PCR amplification for MLC parts and prepped the PCR mix with the concentrator kit. Conducted the following simple recombination: pSB1C3 + MLC1/2/3/4. Made a liquid culture for the BBa_K1033916/BBa_J61100/pSB1C3 plasmid.

June 20th, 2015

Sean

Transformation

Transformed the simple recombination results (MLC1-4 + backbone).

June 21th, 2015

Sean

Transformation, Liquid Cultures

Retransformed the simple recombination results due to bad colony growth. Made liquid cultures for MLC1, MLC2 (#1 and #2) and MLC 3.

Elliot

Agarose Gel Electrophoresis

Ran a 1% gel with the following specifications: 1: 1 kb ladder; 2: BBa_E1010#1/BBa_J61100/pSB1C3, undigested; 3: BBa_E1010#1/BBa_J61100/pSB1C3, EcoRI digestion; 4: BBa_E1010#1/BBa_J61100/pSB1C3, SpeI digestion; 5: BBa_E1010#1/BBa_J61100/pSB1C3, double digest; 6: BBa_E1010#3/BBa_J61100/pSB1C3, undigested; 7: BBa_E1010#3/BBa_J61100/pSB1C3, EcoRI digestion; 8: BBa_E1010#3/BBa_J61100/pSB1C3, SpeI digestion; 9: BBa_E1010#3/BBa_J61100/pSB1C3, double digest; 10: 1 kb ladder.

June 22nd, 2015

Jerry

Agarose Gel Electrophoresis

Ran a 1% gel with the following specifications: 1: 100 bp ladder; 2: MLC1; 3: MLC2; 4: MLC3; 5: MLC4; 6: MLC2#1/BBa_J61100/pSB1C3; 7: MLC2#2/BBa_J61100/pSB1C3; 8: MLC3/BBa_J61100/pSB1C3; 9: 1 kb ladder.

June 23rd, 2015

Jerry

3A Assembly

Conducted a 3A assembly with the following components: BBa_J4450 (pSB1C3), BBa_K1033916#2+BBa_J61100/BBa_K592009+BBa_J61100, BBa_K861171/ BBa_K118011. Only managed to get to the digestion step, stored for Connors’ usage tomorrow. Connor

Zyppy Plasmid Miniprep

Miniprepped the MLC1/2(1)/2(2)/3+pSB1C3 liquid cultures. Made more LB stock.

June 24th, 2015

Connor

3A Assembly, Zyppy Plasmid Miniprep

Finished the ligation step of 3A assembly and stored the plasmids in the freezer. Made glycerol stocks for MLC 1/2/3 (1 is mislabeled as 4!). Miniprepped the MLC1+pSB1C3 construct and nanodropped for concentration determination.

June 26th, 2015

Elliot

ZR Plasmid Miniprep Classic

Miniprepped 3 BBa_K1033916/BBa_J61100/pSB1C3 construct liquid cultures

July 1st, 2015

Elliot

Liquid Cultures, Transformation

Made liquid cultures for the BBa_1033916/BBa_J61100/pSB1C3 and the BBa_K118011/BBa_K592009+BBa_J61100/pSB1C3 constructs. Also plated the BBa_K118011/BBa_K592009+BBa_J61100/pSB1C3 and BBa_K861171/BBa_1033916+BBa_J61100/pSB1C3 constructs once more.

Connor

3A Assembly

Constructed a plasmid with the following components: BBa_E1010+BBa_J61100 + BBa_K4450 + MLC1/2(1)/2(2)/3.

July 2nd, 2015

Connor

Transformation/Liquid Culture

Transformed the 3A assembly results from yesterday (BBa_E1010/BBa_J61100 + BBa_K4450 + MLC1/2(1)/2(2)/3). Also made liquid cultures of the BBa_K118011/BBa_K592009+BBa_J61100/pSB1C3 and BBa_K861171/BBa_1033916+BBa_J61100/pSB1C3 constructs. *NOTE: plates were overgrown during selection!

July 3rd, 2015

Connor

3A Assembly/Transformation/Liquid Culture

Attempted another ligation with the backbone (BBa_J4450) and MLC4 digests. Transformed the result. Made liquid cultures of MLC composite parts (BBa_E1010/BBa_J61100 + BBa_K4450 + MLC1/2(1)/2(2)/3).

*Note: The MLC4 ligation culture failed to grow.

Elliot

ZR Plasmid Miniprep Classic

Miniprepped the BBa_K118011/BBa_K592009+BBa_J61100/pSB1C3 and BBa_K861171/BBa_1033916+BBa_J61100/pSB1C3 constructs. Nanodropped and found no DNA, so discarded.

*Note: Liquid cultures had a cellular deposit on the bottom for some reason

July 4th, 2015

Connor

ZR Plasmid Miniprep Classic/Liquid Cultures

Miniprepped the MLC Composite Parts (BBa_E1010/BBa_J61100 + BBa_K4450 + MLC1/2(1)/2(2)/3). Nanodropped and stored the results. Made liquid cultures of the BBa_K118011/BBa_K592009+BBa_J61100/pSB1C3 and BBa_K861171/BBa_1033916+BBa_J61100/pSB1C3 constructs

July 6th, 2015

Connor

Simple Recombination/Agarose Gel Electrophoresis/Transformation

Attempted simple recombination with MLC4 and pSB1C3. Transformed the result. Ran a 1% gel with the following specifications: 1. 1 kb ladder; 2. 100 bp ladder; 3. MLC1/BBa_E1010/pSB1C3 (E+P cut); 4. MLC2(1)/BBa_E1010/pSB1C3 (E+P cut); 5. MLC2(2)/BBa_E1010/pSB1C3 (E+P cut); 6. MLC3/BBa_E1010/pSB1C3 (E+P cut).

July 7th, 2015

Connor and Jerry

ZR Plasmid Miniprep Classic/Agarose Gel Electrophoresis

Miniprepped liquid cultures from the red and white colonie on the MLC Composite Parts plates and the BBa_K118011/BBa_K592009+BBa_J61100/pSB1C3 and BBa_K861171/BBa_1033916+BBa_J61100/pSB1C3 constructs. Ran a 1% gel with the following specifications: 1. 1 kb ladder; 2. 100 bp ladder; 3. MLC1/BBa_E1010/pSB1C3 (E+P cut) (Red); 4. MLC2(1)/BBa_E1010/pSB1C3 (E+P cut) (Red); 5. MLC2(2)/BBa_E1010/pSB1C (E+P cut) (Red)3; 6. BBa_K861171/BBa_1033916+BBa_J61100/pSB1C3 (E+P cut); 7. BBa_K118011/BBa_K592009+BBa_J61100/pSB1C3 (E+P cut); 8. MLC1/BBa_E1010/pSB1C3 (E+P cut) (White); 4. MLC2(1)/BBa_E1010/pSB1C3 (E+P cut) (White); 5. MLC2(2)/BBa_E1010/pSB1C (E+P cut) (White).

July 8th, 2015

Connor

Liquid Cultures

Made liquid cultures of the BBa_K118011/BBa_K592009+BBa_J61100/pSB1C3 and BBa_K861171/BBa_1033916+BBa_J61100/pSB1C3 constructs.

July 9th, 2015

Connor

ZR Plasmid Miniprep Classic

Miniprepped the BBa_K118011, BBa_K861171, BBa_K592009, BBa_K1033916, BBa_E1010 and BBa_E1010/BBa_J61100 constructs and nanodropped. Made glycerol stocks of all.

July 10th, 2015

Connor and Jerry

Liquid Culture/Transformation

Transformed BBa_B0034 from plate 4, well 1N with 10 uL USP water. Transformed and plated with AmpR plates. Made 4 liquid cultures with 1g/L glucose concentration and the MLC Composite Parts to check for chromoprotein expression via glucose induction.

July 11th, 2015

Connor

Liquid Culture/Simple Recombination/Transformation

Made liquid cultures of BBa_B0034 and BBa_J61100. Attempted simple recombination with MLC4(1)/MLC4(2) and pSB1C3. Transformed the ligation result.

July 12th, 2015

Connor

ZR Plasmid Miniprep Classic/Liquid Cultures

Miniprepped the BBa_J61100 and BBa_B0034. Nanodropped and made a glycerol stock of both. Made liquid cultures of the MLC4(1)/pSB1C3 and MLC4(2)/pSB1C3 constructs.

July 13th, 2015

Connor

ZR Plasmid Miniprep Classic/3A Assembly/Agarose Gel Electrophoresis/Transformation

Miniprepped the MLC4(1)/pSB1C3 and MLC4(2)/pSB1C3 constructs. Conducted 3A assembly to make the following parts: BBa_K1033916/BBa_B0034; BBa_K1033916/BBa_J61100; BBa_K592009/BBa_B0034; BBa_K592009/BBa_J61100; BBa_E1010/BBa_B0034; BBa_E1010/BBa_J61100. Transformed the ligation results. Ran a 1% gel with the following specifications: 1. 100 bp ladder; 2. 1 kb ladder; 3. MLC4(1)/pSB1C3; 4. MLC4(2)/pSB1C3; 5. pSB1C3(1); 6.pSB1C3(2).

July 14th, 2015

Jerry

PCR

Amplified the MLC4 fragment

July 15th, 2015

Elliot

Transformation

Plated BBa_K1033931, BBa_K1073023, and BBa_K1033929.

July 16th, 2015

Connor and Jerry

DNA Clean and Concentrator Prep

Prepped the MLC4 PCR results and nanodropped.

Jerry

Agarose Gel Electrophoresis/PCR

Ran a 1% gel with the following specifications: 1. 100 bp ladder; 2. 1 kb ladder; 3. MLC4; 4. BBa_K1033931; 5. BBa_E1010. Amplified the MLC1-3 fragments with PCR.

July 17th, 2015

Connor

DNA Clean and Concentrator Prep/Agarose Gel Electrophoresis

Prepped the MLC1-3 PCR Results and nanodropped. Ran a 1% gel with the following specifications: 1. 1 kb ladder; 2. 100 bp ladder; 3. MLC1; 4. MLC2; 5. MLC3; 6. MLC4.

Jerry/Elliot

Liquid Culture

Made 2 liquid cultures of BBa_K1073025, BBa_K1073023 and BBa_K1073021 each. Also made liquid cultures of each of the MLC+pSB1C3 constructs.

July 18th, 2015

Elliot

ZR Plasmid Miniprep Classic/3A Assembly

Miniprepped BBa_K1033931, BBa_K1033929, and BBa_K1073023. Nanodropped and created the following constructs with 3A: BBa_K118011/BBa_K1073023 and BBa_K861171/BBa_K1033929.

Connor

Transformation

Transformed the following constructs: BBa_K861171/BBa_K1033929; BBa_K118011/BBa_K1073023; MLC1/pSB1C3; MLC2/pSB1C3; MLC3/pSB1C3; MLC4/pSB1C3.

July 20th, 2015

Connor

Liquid Culture/Agarose Gel Electrophoresis

Made liquid cultures for each of the MLC Constructs in backbones. Ran a 1% gel with the following specifications: 1. 100 bp ladder; 2. 1 kb ladder; 3. BBa_K118011/BBa_K1073023 (1) (White); 4. BBa_K118011/BBa_K1073023 (2) (White); 5. BBa_K118011/BBa_K1073023 (1) (Red); 6. BBa_K118011/BBa_K1073023 (2) (Red); 7. BBa_K861171/BBa_K1033929 (1); 8. BBa_K861171/BBa_K1033929 (2).

July 21st, 2015

Connor/Elliot

Agarose Gel Electrophoresis

Ran a 1% gel with the following specifications: 1. 1 kb ladder; 2. 100 bp ladder; 3. BBa_K118011/BBa_K1073023 (1) (White) (E+P cut); 4. BBa_K118011/BBa_K1073023 (2) (White) (E+P cut); 5. BBa_K118011/BBa_K1073023 (1) (Red) (E+P cut); 6. BBa_K118011/BBa_K1073023 (2) (Red) (E+P cut); 7. BBa_K861171/BBa_K1033929 (1) (E+P cut); 8. BBa_K861171/BBa_K1033929 (2) (E+P cut).

July 23rd, 2015

Jerry

Agarose Gel Electrophoresis

Ran a 1% gel with the following specifications (all E+P cut): 1. 1 kb ladder; 2. 100 bp ladder; 3. MLC1/pSB1C3 (a); 4. MLC1/pSB1C3 (b); 5. MLC1/pSB1C3 (c); 6. MLC2/pSB1C3 (b); 7. MLC2/pSB1C3 (c); 8. MLC3/pSB1C3 (b); 9. MLC4/pSB1C3 (a); 10. MLC4/pSB1C3 (b); 11. BBa_K861171/BBa_K1033929; 12. BBa_K118011/BBa_K1073023; 13. 100 bp ladder; 14. 1 kb ladder.

July 29th, 2015

Jerry

Liquid Culture

Made liquid cultures of BBa_K118011 and BBa_K861171. Also plated the BBa_K1073023, BBa_K1033929, and BBa_K1033931 sent from the registry.

July 30th, 2015

Jerry

ZR Plasmid Miniprep Classic

Miniprepped the BBa_K118011 and BBa_K861171 cultures. Nanodropped the result.

July 31st, 2015

Jerry

3A Assembly/Simple Recombination/Agarose Gel Electrophoresis

Conducted a 3A to create the following constructs: BBa_K861171/BBa_K1033929 and BBa_K118011/BBa_K1073023. Attempted to recombine the MLC fragments into the pSB1C3 backbone. Ran a 1% gel with the following specifications: 1. 1 kb ladder; 2. 100 bp ladder; 3. pSB1C3 (E cut); 4. pSB1C3 (P cut); 5. pSB1C3; 6. MLC1 (E+S cut); 7. MLC2 (E+S cut); 8. MLC3 (E+S cut); 9. MLC4 (E+S cut); 10. pSB1C3 (E+S cut); 11. BBa_K1073023 (P+X cut); 12. BBa_K107029 (P+X cut); 13. BBa_K861171 (P+S cut); 14. BBa_K118011 (P+S cut).

August 1st, 2015

Connor

Transformation

Transformed all the MLC/pSB1C3 constructs with one of the BBa_K118011/BBa_K1073023 (Red) and BBa_K861171/BBa_K1033929 constructs.

August 2nd, 2015

Jerry

Liquid Culture

Made 2 liquid cultures each of the MLC constructs with pSB1C3, BBa_K118011/BBa_K1073023, and BBa_K861171/BBa_K1033929.

August 3rd, 2015

Jerry

Transformation

Transformed the reconstituted BBa_J23119 (plate 3, well 17) along with two of the BBa_K118011/BBa_K1073023 constructs and one of the BBa_K861171/BBa_K1033929 constructs.

Jerry and Sean

ZR Plasmid Miniprep Classic

Prepped the MLC+pSB1C3, BBa_K118011/BBa_K1073023, and BBa_K861171/BBa_K1033929 constructs. Nanodropped the results.

August 4th, 2015

Connor

3A Assembly/ZR Plasmid Miniprep Classic

Attempted a 3A to make the following constructs: MLC1/BBa_K1033931; MLC2/BBa_K1033931; MLC3/BBa_K1033931; MLC4/BBa_K1033931. Miniprepped the pSB1C3 liquid cultures and nanodropped.

Sean

Elongated Digestion/DNA Clean and Concentrator Prep/Elongated Ligation

Digested BBa_J23119, BBa_K1033931, BBa_K1073023, and BBa_K1033929 for 2 hours. Prepped the digestion results and nanodropped. Ligated and left overnight.

Elliot

Transformation

Transformed MLC1-4+pSB1C3.

August 5th, 2015

Connor/Elliot

Liquid Culture/Transformation/Agarose Gel Electrophoresis

Made 4 liquid cultures of the MLC/BBa_K1033931 Constructs. Transformed the constitutive promoter (BBa_J23119)+chromoprotein constructs. Ran a 1% gel with the following specifications: 1. 1 kb ladder; 2. 100 bp ladder; 3. BBa_K118011/BBa_K1073023 (1); 4. BBa_K118011/BBa_K1073023 (2); 5. BBa_K861171/BBa_K1033929 (1); 6. BBa_K861171/BBa_K1033929 (2).

August 6th, 2015

Elliot

ZR Plasmid Miniprep Classic

Miniprepped the MLC1-4/pSB1C3/BBa_K1033931 liquid cultures and nanodroppped.

Sean DNA Clean and Concentrator Prep/Elongated Ligation

Prepped the digestion results of BBa_K861171, BBa_K118011, BBa_K1033929, and BBa_K1073023. Ligated and left overnight.

August 7th, 2015

Connor

Transformation

Transformed 2 uL of reconstituted pSB1A3 from plate 4, well 2H.

August 1th, 2015

Connor

Liquid Culture

Made a liquid culture of pSB1A3.

August 10th, 2015

Elliot

Transformation

Transformed 2 uL of reconstituted pSB1A3 from plate 4, well 2H.

August 11th, 2015

Elliot

Liquid Culture

Made a liquid culture of pSB1A3.

August 12th, 2015

Jerry/Sean

Elongated Digestion/Agarose Gel Electrophoresis

Digested MLC+pSB1C3, BBa_K861171, and BBa_K118011 at S+P. Digested BBa_K1033929, BBa_K1073023 and BBa_K1033931 at X+P. Digested for 3 hours in total. Ran a 1% gel with the following specifications: 1. 1 kb ladder; 2. BBa_K1073023; 3. BBa_K1033929; 4. BBa_K1033931; 5. BBa_K118011; 6. BBa_K861171; 7. MLC1+pSB1C3; 8. MLC2+pSB1C3; 9. MLC+pSB1C3; 10. BBa_J23119.

Sean

Gel Purification Prep/Elongated Ligation

Ran the digestion results on a gel and purified. Nanodropped and made ligation mixes for 3 hour incubation.

Elliot

Transformation

Transformed the final ligation mixtures, including BBa_K118011/BBa_K1073023, BBa_K861171/BBa_K1033931, and MLC1-4/BBa_K1033929.

August 13th, 2015

Elliot

Transformation

Retransformed the final ligation mixtures, including BBa_K118011/BBa_K1073023, BBa_K861171/BBa_K1033931, and MLC1-4/BBa_K1033929.

August 14th, 2015

Jerry and Sean

Elongated Digestion

Digested MLC+pSB1C3, BBa_K861171, and BBa_K118011 at S+P. Digested BBa_K1033929, BBa_K1073023 and BBa_K1033931 at X+P. Digested for 3 hours in total.

August 18th, 2015

Sean

DNA Clean and Concentrator/Gel Purification Prep/Elongated Ligation

Prepped the promoter parts with the concentrator kit and selected for the correct chromoproteins with the gel purification prep. Ligated BBa_J23119 and BBa_K118011 with BBa_K1073023 and left for 3 hours.

Connor

Transformation/Liquid Culture

Transformed the red chromoprotein+constitutive promoter construct and the BBa_K118011/BBa_K1073023 construct. Made liquid cultures of all of the MLC/pSB1C3 constructs, BBa_1033931, and BBa_K1033929.

August 19th, 2015

Connor

ZR Plasmid Miniprep Classic/Liquid Culture

Miniprepped BBa_J23119 and BBa_K1073023. Made liquid cultures of BBa_K118011, BBa_K861171, BBa_K1073023, BBa_K1033931, BBa_K1033929, the MLC1-4+pSB1C3 constructs and BBa_J23119.

August 20th, 2015

Connor

ZR Plasmid Miniprep Classic

Miniprepped BBa_K118011, BBa_K861171, BBa_K1073023, BBa_K1033931, BBa_K1033929, the MLC1-4+pSB1C3 constructs and BBa_J23119 and nanodropped for concentration.

August 21st, 2015

Connor

Elongated Digestion/Gel Purification Prep/Elongated Ligation

Digested 2500 ng of BBa_K118011, BBa_K861171, BBa_K1073023, BBa_K1033931, BBa_K1033929, the MLC1-4+pSB1C3 constructs and BBa_J23119 each for 3 hours. Ran on a 1% gel and purified with the kit. Ligated overnight.

August 22nd, 2015

Connor

Transformation

Transformed the ligation mixes of BBa_K118011, BBa_K861171, BBa_K1073023, BBa_K1033931, BBa_K1033929, the MLC1-4+pSB1C3 constructs and BBa_J23119. Incubated overnight.

August 26th, 2015

Connor

ZR Plasmid Miniprep

Miniprepped BBa_K118011/BBa_K1073023, BBa_K861171/BBa_K1073023, and the MLC2 construct/BBa_K1033931.

Jerry

PCR

Amplified the PCR Constructs with a 32 cycle PCR.

August 27th, 2015

Sean

PCR

Amplified the PCR Constructs with a 35 cycle PCR and left overnight in the freezer.

August 28th, 2015

Sean and Jerry

DNA Clean and Concentrate Prep/Elongated Digestion

Cleaned the completed PCR solutions with the prep. Nanodropped for concentrations. Digested the PCR constructs with pSB1C3 and incubated for three hours.

Connor

DNA Clean and Concentrator Prep/Ligation

Prepped the digested PCR constructs and ligated into the digested pSB1C3 backbone. Incubated overnight.

August 29th, 2015

Connor

Transformation

Transformed the ligated PCR+pSB1C3 constructs. Incubated overnight.

August 30th, 2015

Elliot

Transformation

Transformed pSB1C3 stocks and plated. Incubated overnight.

August 31st, 2015

Connor

PCR/DNA Clean and Concentrator Kit/Elongated Digestion/Elongated Ligation

Conducted a 32 cycle PCR amplification of the PCR constructs. Cleaned with the kit and nanodropped. The results were then digested with miniprepped pSB1C3 and cleaned again after a 2 hour incubation. The PCR constructs were then ligated with the digested pSB1C3 and incubated overnight.

September 1st, 2015

Jerry

Transformation/PCR

Transformed the PCR Construct ligation mixes and incubated overnight. Set a 32 cycle PCR to amplify more of the base PCR constructs.

September 2nd, 2015

Connor

Liquid Culture

Made liquid cultures of the MLC/BBa_K1033931 PCR constructs, the BBa_J23119/BBa_K1073023 PCR construct, the BBa_K861171/BBa_K1073023 PCR construct, the BBa_K118011/BBa_K1033929 PCR construct and the tripart constructs.

September 3rd, 2015

Connor

ZR Plasmid Miniprep Classic

Miniprepped the MLC/BBa_K1033931 PCR constructs, the BBa_J23119/BBa_K1073023 PCR construct, the BBa_K861171/BBa_K1073023 PCR construct, the BBa_K118011/BBa_K1033929 PCR construct and the tripart constructs.

September 4th, 2015

Jerry

ZR Plasmid Miniprep Classic

Miniprepped the viable PCR Construct liquid cultures and nanodropped.

Connor

PCR/DNA Clean and Concentrator Kit/Elongated DIgestion/Elongated Ligation

Conducted a 32 cycle PCR amplification of the PCR constructs. Cleaned with the kit and nanodropped. The results were then digested with miniprepped pSB1C3 and cleaned again after a 2 hour incubation. The PCR constructs were then ligated with the digested pSB1C3 and incubated overnight.

September 5th, 2015

Will

DNA Clean and Concentrator Prep/Elongated Ligation

Prepped the BBa_J23119/BBa_K1033931 and BBa_J23119/BBa_K1033929 PCR constructs. Ligated with digested pSB1C3 and incubated overnight.

Connor

Transformation

Transformed the ligated PCR constructs+pSB1C3. Incubated overnight.

September 6th, 2015

Elliot

Liquid Cultures/Transformation

Created liquid cultures of the viable PCR constructs and transformed the BBa_J23119/BBa_K1033931 and BBa_J23119/BBa_K1033929 PCR constructs. Incubated overnight.

September 7th, 2015

Elliot

ZR Plasmid Miniprep Classic

Miniprepped the liquid cultures of the viable PCR constructs.

September 8th, 2015

Connor

PCR/Transformation

Transformed the the ligated PCR constructs+pSB1C3. Incubated overnight. Also ran a 32 cycle PCR amplification of the BBa_J23119/BBa_K1033931 and BBa_J23119/BBa_K1033929 PCR constructs.

September 10th, 2015

Connor

ZR Plasmid Miniprep Classic/PCR/Liquid Cultures/DNa Clean and Concentrator Prep

Miniprepped the three MLC PCR Constructs. Amplified the BBa_J23119/BBa_K1033931, BBa_J23119/BBa_K1033929, BBa_J23119/BBa_K1073023, BBa_K861171/BBa_K1073023, MLC1/BBa_K1033931, and Tripart PCR constructs with a 32 cycle PCR. Made liquid cultures of pSB1C3 and BBa_B0034 and used the clean kit to prep the PCR products.

September 11th, 2015

Connor

ZR Plasmid Miniprep Classic/Elongated Ligation/Elongated Digestion/Transformation

Miniprepped the pSB1C3 and BBa_B0034 cultures. Digested the PCR constructs, pSB1C3 and BBa_B0034 stocks and incubated for two hours. Ligated the PCR constructs together with the backbones and incubated for 3 hours. Transformed and incubated overnight.

September 12th, 2015

Connor

Liquid Cultures

Prepared liquid cultures of the BBa_J23119/BBa_K1073023, BBa_J23119/BBa_K1033929, and BBa_K118011/BBa_K1033929 PCR constructs.

September 13th, 2015

Jerry

Characterized the sensitivity parts by varying the amount of glucose concentrations in liquid cultures and monitoring their growth and changes in absorbance over time and with based on glucose concentrations.

Connor

ZR Plasmid Miniprep Classic

Miniprepped pSB1C3 liquid cultures and the BBa_K861171/BBa_K1073023 stocks. Nanodropped and stored.

September 14th, 2015

Connor

Elongated Digestion/Elongated Ligation/Transformation

Digested three pSB1C3 stocks and one BBa_B0034 stock along with 500 ng of purified PCR constructs. Incubated for three hours. Ligated together to insert the constructs into the backbone and incubated for 3 hours. Transformed and incubated overnight.

September 15th, 2015

Connor

Liquid Culture

Made liquid cultures of all of the viable PCR constructs, excluding the MLC1 construct and the full constructs.