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• Start
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  • Laccases
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For measuring the Laccase activity we detected the level of oxidized ABTS via optical density at 420nm. The device we were able to use was a [http://www.tecan.com/platform/apps/product/index.asp?MenuID=1812&ID=1916&Menu=1&Item=21.2.10.1 Tecan Infinite Reader M200]. The program setup was in some parts adapted to the needs of our probes (like duration of the measurement) and in some parts standardized.
Used setup for Laccase activity measurements: Temperature: 25°C; Orbital shaking before each measuring cycle (time depends on duration of each cycle); Number of flashes: 30

Maldi-TOF

Matrix-assisted Laser Desorption/Ionization – Time of flight (MALDI-TOF) is a procedure to analyze large biomolecules by their mass.

Before measurement, the analyte is co-crystallized on a metal plate within a solid matrix. 3,5-dimethoxy-4-hydroxycinnamic acid (sinapinic acid) and 2,5-dihydroxybenzoic acid (DHB) are most commonly used. Desorption of the analyte is taken by a laser beam, commonly with a wavelength of 337 nm. The matrix absorbs the laser light and the upper layer explosively vaporizes, ejecting both, matrix and analyte molecules. In addition to this vaporization, the laser beam also leads to an ionization of the analytes. The mass analysis is performed by the TOF (time of flight)-analysator. The evaporated ions are accelerated in an electric field. Typical acceleration voltages for this are 10-30 kV. The velocity of an ion depends on its mass and the charge. An ion detector converts the incoming ions into an electrical signal. The advantage of this method is the rapid analysis of a relatively large mass range.

The MALDI-TOF analysis was performed with the [http://www.bdal.com/products/maldi/ultraflextreme-series/overview.html ultrafleXtreme™] by Bruker Daltonics.

We used the MALDI-TOF Analysis to characterize the following BioBricks: ???????????

ÄKTAprime plus Chromatographiesystem

ÄKTA is a Swedish word that means true, genuine, or real. ÄKTAprime plus is a compact pumping system which can be used for a range of columns, chromatography media, and filters. This device is ease-of-use and present a high flexibility of liquid handling and minimizing the problem of sample loss.This system can record pH-value, pressure, conductivity, UV-absorption and the flowrate. Different programms are available like PrimeView™ software to evaluate the recorded data.

We used this system to purify our produced laccases with a Immobilized Metal Ion Affinity Chromatography strategy.

The Precellys® 24 homogenizer

[http://www.peqlab.de/wcms/en/pdf/91-PCS24.pdf The Precellys® 24] is an effective and efficient sample homogenisation to enable effective DNA, RNA or protein extraction. To disrup tumor tissues, hair, cartilages, bones, plant materials, yeasts, bacterium and fungi the samples are loaded in beads containing 2 ml tubes. The tubes can be supplied with steel, ceramic or glass beads. The homogenization effect takes place during a 3-dimensional figure of eight motion. This lead to strong acceleration of the used beads. The forces between the beads and the collisions induce the disruption of cell or the homogenisation of samples.

The first cell disruptions ot the iGEM-team Bielefeld were made by this system.

Bioreactors

For the production of the different laccases we used three different variations of bioreactors. These Bioreactors includes different kinds of sonsors:

• pO₂
• pCO₂
• pH
• airflow
• agitation
• temperatur
• antifoam/level

The process could be monitored and controlled by a bioreactor specific programm.

Infors labfors fermenter

Device specifications:

• Vessel: 3.6; total volume
• Speed range: 100–1200 rpm magnetic drive
• Temperature range: ~5°C above coolant to 60°C (water jacket)
• Pump flow rate: 0.001–1.4 mL/min (small-size tubing)
• Special features: autoclavable fermenter
• Standard parameters:
• Stirrer speed, temperature, pH, pO2, antifoam/level, feed, gas

mix, gas flow

Biostat B Bioreactor (3 L) by Braun

Device specifications:

• Vessel: 3,5; total volume
• Speed range: 100–1200 rpm magnetic drive
• Temperature range: ~5°C above coolant to 90°C (water jacket)
• Pump flow rate: 0.001–1.4 mL/min
• Special features: autoclavable fermenter
• Standard parameters:
• Stirrer speed, temperature, pH, pO2, antifoam/level, feed, gas

mix, gas flow

Bioreactor NLF (7L) by BIOENGINEERING

Device specifications:

• Vessel: 7; total volume
• Speed range: 100–3000 rpm magnetic drive
• Temperature range: up to 150°C
• Pump flow rate: 50 mL/min
• Standard parameters:
• Stirrer speed, temperature, pH, pO2, antifoam/level, feed, gas

mix, gas flow

Media, buffer and other solutions

Ampicillin stock solution

• Solubilize 100 mg mL^-1 Ampicillin
• Store at -20 °C

Chloramphenicol stock solution

• Solubilize 20 mg mL^-1 Chloramphenicol in 100 % Ethanol
• Store at -20 °C

TAE buffer

For 1 L of 50 x TAE buffer you need:

• 242.48 g Tris
• 41.02 g Sodiumacetate
• 18.612 g EDTA
• Adjust pH to 7.8 with acetic acid
• Solve in dH₂O

10 mL of the stock is diluted in 1 L dH₂O for the gel electrophoresis (0.5 x TAE buffer).

Briton Robinson Buffer

• 0,1 mM acetic acid
• 0,1 mM boric acid
• 0,1 mM phosphoric acid
• adjust to pH 5 with sodium hydroxide

DNA loading buffer

• 50 % (v/v) glycerol
• 1 mM EDTA
• 0.1 % (w/v) bromphenol blue
• Solve in ddH₂O

LB medium

For 1 L of LB medum:

• 10 g Trypton
• 5 g Yeast extract
• 10 g NaCl
• 12 g Agar-Agar (for plates)
• Adjust pH to 7.4

Autoinduction medium

The Autoinduction medium is based on LB-medium. Add the following components after heat sterilization of 900 mL LB medium.

• 5 mL of a 200 g L-1 steril L-rhamnose stock solution -> final concentration 2 g L-1
• 2.5 mL of a 200 g L-1 steril glucose stock solution -> final concentration 1 g L-1
• if necessary add antibiotics:

Cm: 1 mL or 3 mL of a 20 μg mL-1 Cm stock solution -> final concentration 20 or 60 mg L-1

Amp: 1 mL or 3 mL of a 100 μg mL-1 Amp stock solution -> final concentration 100 or 300 mg L-1

• fill up to 1 L with steril ddH2O

YPD media

For 1 L of YPD media:

• 20 g Peptone
• 10 g Yeast extract
• 20 g Dextrose (add 50 mL sterile stock solution (40% dextrose))
• Adjust pH to 6.5
• For plates: add 17 g/L agar.

Yeast Nitrogen Base (YNB) 10x stock solution

• Dissolve 69 g Yeast Nitrogen Base (without aminoacids; with ammonium sulfat) in 500 mL bidest water and filter sterilize.
• Store at 4 °C.
• Durable for one year.

Biotin 500x stock solution

• Dissolve 20 mg biotin in 100 mL of 0.05 M NaOH solution and filter sterilize.
• Store at 4 °C.
• Durable for one year.

MD agar plates for selection of recombinant His⁺ clones

For 1 L MD agar plates you need:

• Autoclave 2 g dextrose and 15 g agar
• add 100 mL sterile 10x YNB stock solution and
• 2 mL sterile 500x biotin stock solution.

BEDS buffer

For 1 L of BEDS buffer:

• 1,85 g bicine-sodium salt,
• 30 mL ethylene glycol (final concentration 3%(v/v))
• 50 mL (v/v) dimethyl sulfoxide (DMSO)(final concentration 5%(v/v))
• 182.17 g sorbitol
• Adjust pH at 8,3

Dithiothreitol-Solution (DTT)

For 50mL of DTT-Solution:

• 7.71 g Dithiothreitol

special buffers for resuspending the cell pellet

for KRX and KRX with [http://partsregistry.org/wiki/index.php?title=Part:BBa_K863015 BBa_K863015] and [http://partsregistry.org/wiki/index.php?title=Part:BBa_K863005 BBa_K863005]:

• sodium acetate 100 mM
• adjust to pH 5

for KRX with [http://partsregistry.org/wiki/index.php?title=Part:BBa_K863010 BBa_K863010]:

• sodium acetate 20 mM
• adjust to pH 5

for KRX with [http://partsregistry.org/wiki/index.php?title=Part:BBa_K863000 BBa_K863000]: [http://www.aeisner.de/rezepte/puffer1.html Mc Ilvaine buffer]

• solution A: 21,01 g/L citric acid
• solution B: 35,60 g/L disodium phosphate dihydrate
• mix 38,6 mL of solution B and 61,4 mL of solution A
• adjust to pH 4

for KRX with [http://partsregistry.org/wiki/index.php?title=Part:BBa_K863020 BBa_K863020]:

• 1 mM CuSO₄
• 15 mM PBS mit K₂HPO₄
• 100 mM NaCl
• adjust to pH 7 and shake before use

Buffers for His-Tag affinity chromatography

• Adjust pH to 7.4 - 7.6

Buffer for Ni-NTA-HisTag affinity chromatography

Buffer	Sodium phosphate [mM]	Imidazole [mM]
Binding buffer	50	20
Elution buffer	50	500

Buffer for Talon-HisTag affinity chromatography

Buffer	Sodium phosphate [mM]	NaCl [mM]	Imidazole [mM]
Binding buffer	50	300	0
Elution buffer	50	300	150

SDS-PAGE gel

The following amouts are for one gel. Stacking gel 5 %:

• 775 μL H₂O
• 1.25 mL 0,25 M Tris (pH 6,8)
• 425 μL Bis/Acrylamide (0,8 %, 30 %)
• 50 μL 5 % SDS
• 25 μL 10 % Ammonium persulfate
• 3 μL TEMED

Separating gel 12 %:

• 1.5 mL H₂O
• 2.8 mL 1 M Tris (pH 8,8)
• 3.0 mL Bis/ Acrylamide (0,8%, 30%)
• 150 μL 5% SDS
• 37.5 μL 10% Ammonium persulfate
• 5 μL TEMED

SDS running buffer

• 25 mM Tris [pH 8,3]
• 192 mM Glycerol
• 0.1 % SDS

4x Laemmli-buffer

• 250 mM Tris-HCl
• 40 % [v/v] Glycerol
• 20 % [v/v] 2-Mercapthoethanol
• 80 g L^-1 SDS
• 0.04 g L^-1 BPB

Fixer solution

• 10 % [v/v] acetic acid
• 25 % [v/v] 2-propanol
• 65 % [v/v] H₂O

Solutions for Gibson assembly

5x isothermal reaction buffer for Gibson assembly

• 3 mL of 1 M Tris-HCl (pH 7.5)
• 150 µL of 2 M MgCl2
• 60 µL of 100 mM dGTP
• 60 µL of 100 mM dATP
• 60 µL of 100 mM dTTP
• 60 µL of 100 mM dCTP
• 300 µL of 1 M DTT
• 1.5 g PEG-8000
• 300 µL of 100 mM NAD

storage -20˚C

Hanks Buffered Saline Solution (HBSS)

• 0.137 M NaCl
• 5.4 mM KCl
• 0.25 mM Na2HPO4
• 0.44 mM KH2PO4
• 1.3 mM CaCl2
• 1.0 mM MgSO4
• 4.2 mM NaHCO3

Primers

This is a list of primers we have used.

primer name	length	sequence
F	28	GTTTCTTCGAATTCGCGGCCGCTTCTAG
R	29	GTTTCTTCCTGCAGCGGCCGCTACTAGTA
pSB1C3-5aox1-f	60	CGCTAAGGATGATTTCTGGAATTCGCGGCCGCTTCTAGAGAGATCTAACATCCAAAGACG
pSB1C3-5aox1-r	30	GGTGGCGGCGGGCGTTTCGAATAATTAGTT
5aox1-mfalpha1-f	68	AGAAGATCAAAAAACAACTAATTATTCGAAACGCCCGCCGCCACCATGAGATTTCCTTCAATTTTTAC
5aox1-mfalpha1-r	20	AGCTTCAGCCTCTCTTTTCT
mfalpha1-aarI-taox1-f	80	GTATCTCTCGAGAAAAGAGAGGCTGAAGCTACACGCAGGTGGTATGTATCACCTGCGTGTCT TGCTAGATTCTAATCAAG
mfalpha1-aarI-taox1-r	20	TAAGCTTGCACAAACGAACT
taox1-phis4-f	60	GTACAGAAGATTAAGTGAGAAGTTCGTTTGTGCAAGCTTATCATGCCATGGACAAGATTC
taox1-phis4-r	20	GGCCGCTCGAGTATTCAGAA
phis4-kozak-his4-f	72	AATAGTTTACAAAATTTTTTTTCTGAATACTCGAGCGGCCCCCGCCGCCACCATGACATTTCCCTTGCTACC
phis4-kozak-his4-r	30	TTATTATTTCTCCATACGAACCTTAACAGC
his4-3aox1-f	60	TCACCGCAATGCTGTTAAGGTTCGTATGGAGAAATAATAACGAGTATCTATGATTGGAAG
his4-3aox1-r	20	AAAACAAGATAGTGCCCCTC
3aox1-pSB1C3-f	60	AGTCTGATCCTCATCAACTTGAGGGGCACTATCTTGTTTTTACTAGTAGCGGCCGCTGCA
3aox1-pSB1C3-r	20	CTCTAGAAGCGGCCGCGAAT
taox-his4-f	61	GTACAGAAGATTAAGTGAGAAGTTCGTTTGTGCAAGCTTAAGATCTCCTGATGACTGACTC
taox-his4-r	27	CTCGGATCTATCGAATCTAAATGTAAG
his4-3aox1-f02	60	TTATTTAGAGATTTTAACTTACATTTAGATTCGATAGATCCGAGTATCTATGATTGGAAG
his4_gi537483_f	46	ACGTgaattcgcggccgcttctagagAGATCTCCTGATGACTGACT
his4_gi537483_r	41	ctgcagcggccgctactagtaGATCTATCGAATCTAAATGT
5'AOX_FW	45	ACGTgaattcgcggccgcttctagagAGATCTAACATCCAAAGACG
5'AOX_RV	41	CTGCAGCGGCCGCTACTAGTACGTTTCGAATAATTAGTTGT
3'AOX_FW	45	ACGTgaattcgcggccgcttctagagCGAGTATCTATGATTGGAA
3'AOX_RV	41	CTGCAGCGGCCGCTACTAGTAAAAACAAGATAGTGCCCCTC
pAOX1_FW	44	ACGTgaattcgcggccgcttctagagcatccgacatccacaggtc
pAOX1_RV	45	CTGCAGCGGCCGCTACTAGTATTCTCAAGTTGTCGTTAAAAGTCG
tAOX1_FW	45	ACGTGAATTCGCGGCCGCTTCTAGAGCTTGCTAGATTCTAATCAA
tAOX1_RV	41	CTGCAGCGGCCGCTACTAGTATAAGCTTGCACAAACGAACT
Ko_alpha_FW	58	ACGTgaattcgcggccgcttctagagcccgccgccaccATGAGATTTCCTTCAATTTT
Ko_alpha_RV	41	CTGCAGCGGCCGCTACTAGTAAGCTTCAGCCTCTCTTTTCT
B.pumi_LAC_FW	44	ACGTGAATTCGCGGCCGCTTCTAGATGAACCTAGAAAAATTTGT
B.pumi_LAC_RV	41	CTGCAGCGGCCGCTACTAGTATTACTGGATGATATCCATCG
B.halo_FW	44	ACGTGAATTCGCGGCCGCTTCTAGATGAAAAAATCATATGGAGT
B.halo_RV	41	CTGCAGCGGCCGCTACTAGTATTACTCAGGCATATTTGGAA
T.thermo_LAC_FW	44	ACGTGAATTCGCGGCCGCTTCTAGATGCTGGCGCGCAGGAGCTT
T.thermo_LAC_RV	41	CTGCAGCGGCCGCTACTAGTACTAACCCACCTCGAGGACTC
E.coli_LAC_FW_T7	79	ACGTGAATTCGCGGCCGCTTCTAGAGtaatacgactcactatagggagagaggagaaaaATGCAACGTCGTGATTTCTT
E.coli_LAC_RV_HIS	62	CTGCAGCGGCCGCTACTAGTATTATTAGTGATGGTGATGGTGATGTACCGTAAACCCTAACA
Xcc_LAC_FW_T7	79	ACGTGAATTCGCGGCCGCTTCTAGAGtaatacgactcactatagggagagaggagaaaaATGTCATTCGATCCCTTGTC
Xcc_LAC_RV_HIS	62	CTGCAGCGGCCGCTACTAGTATTATTAGTGATGGTGATGGTGATGTGCCTCCACCCGCACTT
B.pumi_LAC_FW_T7	79	ACGTGAATTCGCGGCCGCTTCTAGAGtaatacgactcactatagggagagaggagaaaaATGAACCTAGAAAAATTTGT
B. pumi_LAC_RV_HIS	62	CTGCAGCGGCCGCTACTAGTATTATTAGTGATGGTGATGGTGATGCTGGATGATATCCATCG
E.coli_LAC_FW_T7	79	ACGTGAATTCGCGGCCGCTTCTAGAGtaatacgactcactatagggagagaggagaaaaATGCAACGTCGTGATTTCTT
E.coli_LAC_RV_HIS	62	CTGCAGCGGCCGCTACTAGTATTATTAGTGATGGTGATGGTGATGTACCGTAAACCCTAACA
T.thermo_LAC_FW_T7	79	ACGTGAATTCGCGGCCGCTTCTAGAGtaatacgactcactatagggagagaggagaaaaATGCTGGCGCGCAGGAGCTT
T.thermo_LAC_RV_HIS	62	CTGCAGCGGCCGCTACTAGTATTATTAGTGATGGTGATGGTGATGACCCACCTCGAGGACTC
Tv_lac5_FW_oS	38	acgtcacctgcgtgtagctggtatcggtcctgtcgccg
Tv_lac5_RV	39	acgtcacctgcgtgtcaagTTACTGGTCGCTCGGGTCGC
Tv_lac5.P.FW	43	gaattcgcggccgcttctagATGTCGAGGTTTCACTCTCTTCT
Tv_lac5.S.RV	41	CTGCAGCGGCCGCTACTAGTATTACTGGTCGCTCGGGTCGC
Pc_lac35.P.FW	43	gaattcgcggccgcttctagATGTCGAGGTTCCAGTCCCTCTT
Pc_lac35.S.RV	41	CTGCAGCGGCCGCTACTAGTATCAGAGGTCGCTGGGGTCAA
Pc_lac35_FW_oS	38	acgtcacctgcgtgtagctgccatagggcctgtggcgg
Pc_lac35_RV	39	acgtcacctgcgtgtcaagTCAGAGGTCGCTGGGGTCAA
GFP_FW_SV	39	acgtcacctgcgtgtagctCGTAAAGGAGAAGAACTTTT
GFP_RV_SV	41	acgtcacctgcgtgtcaagTTATTTGTATAGTTCATCCATG
J23117_RBS_FW	70	aattcgcggccgcttctagagttgacagctagctcagtcctagggattgtgctagcaaagaggagaaata
J23117_RBS_RV	70	ctagtatttctcctctttgctagcacaatccctaggactgagctagctgtcaactctagaagcggccgcg
J23103_RBS_FW	70	aattcgcggccgcttctagagctgatagctagctcagtcctagggattatgctagcaaagaggagaaata
J23103_RBS_RV	70	ctagtatttctcctctttGCTAGCATAATCCCTAGGACTGAGCTAGCTATCAGctctagaagcggccgcg
J23110_RBS_FW	70	aattcgcggccgcttctagagtttacggctagctcagtcctaggtacaatgctagcaaagaggagaaata
J23110_RBS_RV	70	ctagtatttctcctctttgctagcattgtacctaggactgagctagccgtaaactctagaagcggccgcg
J23103_K_FW	25	CTGACAGCTAGCTCAGTCCTAGGTA
J23110/117_K_FW	25	TTTACGGCTAGCTCAGTCCTAGGTA
T7_K_FW	26	TAATACGACTCACTATAGGGAAAGAG
CBDcex_2AS-Link_Frei	56	CTGCAGCGGCCGCTACTAGTATTAACCGGTGCTGCCGCCGACCGTGCAGGGCGTGC
CBDcex_Freiburg-Prefix	54	GCTAGAATTCGCGGCCGCTTCTAGATGGCCGGCGGTCCGGCCGGGTGCCAGGTG
CBDcex_T7RBS	80	TGAATTCGCGGCCGCTTCTAGAGTAATACGACTCACTATAGGGAAAGAGGAGAAATAATGGGT CCGGCCGGGTGCCAGGT
CBDclos_2ASlink_compl	63	CTGCAGCGGCCGCTACTAGTATTAACCGGTGCTGCCTGCAAATCCAAATTCAACATATGTATC
CBDclos_Freiburg-Prefix	57	GCTAGAATTCGCGGCCGCTTCTAGATGGCCGGCTCATCAATGTCAGTTGAATTTTAC
CBDclos_T7RBS	73	CCGCTTCTAGAGTAATACGACTCACTATAGGGAAAGAGGAGAAATAATGTCAGTTGAATTTTACAACTCTAAC
Cex_Freiburg_compl	54	ACGTCTGCAGCGGCCGCTACTAGTATTAACCGGTGCCGACCGTGCAGGGCGTGC
Clos_Freiburg_compl	56	ACGTCTGCAGCGGCCGCTACTAGTATTAACCGGTTGCAAATCCAAATTCAACATAT
Eco_Freiburg	53	ACGTGAATTCGCGGCCGCTTCTAGATGGCCGGCCAACGTCGTGATTTCTTAAA
Eco_Freiburg_compl	53	ACGTCTGCAGCGGCCGCTACTAGTATTAACCGGTTACCGTAAACCCTAACATC
GFP_Freiburg	54	ACGTGAATTCGCGGCCGCTTCTAGATGGCCGGCCGTAAAGGAGAAGAACTTTTC
GFP_Freiburg_compl	61	ACGTCTGCAGCGGCCGCTACTAGTATTAACCGGTTTTGTATAGTTCATCCATGCCATGTGT
GFP_His6_compl	74	CTGCAGCGGCCGCTACTAGTATTAACCGGTGTGATGGTGATGGTGATGTTTGTATAGTTCATCCATGCCATGTG
GFP_FW	48	ATGCGAATTCGCGGCCGCTTCTAGAGTCCCTATCAGTGATAGAGATTG
S3N10_Cex_compl	40	TTGTTGTTGTTCGAGCTCGAGCCGACCGTGCAGGGCGTGC
S3N10_Clos_compl	40	TTGTTGTTGTTCGAGCTCGAGCTGCCGCCGACCGTGCAGG
S3N10_GFP	40	CAATAACAATAACAACAACCGTAAAGGAGAAGAACTTTTC

Used enzymes

Enzyme	Producer
AarI	[http://www.fermentas.de/product_info.php?info=p166&language=de Fermentas]
AgeI	[http://www.fermentas.de/product_info.php?info=p247 Fermentas]
DpnI	[http://www.fermentas.de/product_info.php?info=p296 Fermentas]
EcoRI	[http://www.fermentas.de/product_info.php?info=p336 Fermentas]
GoTaq DNA-polymerase	[http://www.promega.com/products/pcr/routine-pcr/gotaq-pcr-core-systems/ Promega]
NgoMIV	[http://www.neb.com/nebecomm/products/productR0564.asp NEB]
lysozym	[http://www.carlroth.com/catalogue/catalogue.do;jsessionid=488EF42170F5810F6A64C9ED26264DD7?favOid=000000010000a36800020023&act=showBookmark&lang=de-de&market=AT Carl Roth]
Pfu DNA-polymerase	[http://www.promega.com/products/pcr/routine-pcr/pfu-dna-polymerase/ Promega]
PstI	[http://www.fermentas.de/product_info.php?info=p458 Fermentas]
Phusion HF DNA-polymerase	[http://www.finnzymes.com/pcr/phusion_high_fidelity_dna_polymerase.html Finnzymes]
Shrimp alkaline phosphatase	[http://www.fermentas.de/product_info.php?info=p592 Fermentas]
SpeI	[http://www.fermentas.de/product_info.php?info=p202 Fermentas]
T4-DNA-Ligase	[http://www.fermentas.de/product_info.php?info=p580 Fermentas]
BIOTAQ DNA-polymerase	[http://www.bioline.com/h_prod_detail.asp?itemid=219 Bioline]
XbaI	[http://www.fermentas.de/product_info.php?info=p247 Fermentas]
T5 exonuclease	[http://www.neb.com/nebecomm/products/productM0363.asp NEB]
taq DNA Ligase	[http://www.neb.com/nebecomm/products/productM0208.asp NEB]
PvuII	[http://www.neb.com/nebecomm/products/productr0151.asp NEB]
HindIII	[http://www.neb.com/nebecomm/products/productr0104.asp NEB]

Used Kits

Function	Name
Plasmid purification	[http://www.fermentas.de/product_info.php?info=p874 Fermentas GeneJET™ Plasmid Miniprep Kit]
Plasmid purification	[http://www.promega.com/b/de/minis/default.aspx?utm_source=Promega&utm_medium=Online&utm_campaign=Online_DEPureYield100Preps_Promega_HP_Banner Promega PureYield™ Plasmid Preps]
PCR Cleanup	[http://www.promega.com/products/dna-and-rna-purification/dna-fragment-purification/wizard-sv-gel-and-pcr-clean_up-system/ Promega Wizard® SV Gel and PCR Clean-Up]
PCR core system	[http://www.promega.com/products/pcr/routine-pcr/gotaq-pcr-core-systems/ Promega GoTaq® PCR Core System I]

Substrates

Hormones

• Estradiol
• Estrone
• [http://www.tcichemicals.com/eshop/en/eu/commodity/E0037/ Ethinyl estradiol]

Analgesics

• Diclofenac
• Ibuprofen
• Naproxen

Polycyclic aromatic hydrocarbons

• Naphthalin
• Acenaphthen
• Phenanthren
• Anthracen

Used chemicals

• Acetonitril
• Methanol