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14:39, 31 May 2023 ‎UA Biophysics:Protocols:Carotenoid Extration ESP (hist | edit) ‎[2,813 bytes] ‎Elizabeth Suesca (talk | contribs) (Created page with "==Materiales para 6 gramos de célula== * Preparar centrífuga a 4 grados * 200 ml Metanol. Opcional: Agregar 2,6-Di-tert-butyl-4-methylphenol 0.1 % w/V (250 mg/250 ml) Para la extracción de carotenos, ya que los protegen de oxidación * 500 NaCl 1,7 M (99.348 g/1 L) * 200 Acetato de etilo (Mejor si esta destilado ya que tiende a ser muy hidrófilo) * Opcional Na2SO4 anhidro (1 g/ 500 ml de solución) * Cloroformo")
14:07, 31 May 2023 ‎UA Biophysics:Protocols:Elution Buffer (hist | edit) ‎[1,055 bytes] ‎Elizabeth Suesca (talk | contribs) (Created page with " '''Buffer HEPES: 2 L a 400 mOsM pH 7.4 ==Materiales== MW (g/mol) [] mM mOsM M HEPES 238.30 20 20 9.532 g NaCl 58.44 170 340 19.869 g NaOH (1 M) 8 8 16 ml NaCl 16 32 1.870 g Colocar 1.6 litros de agua deionizada en la botella Pesar el HEPES y el NaCl, diluir en los 1,6 L de dH2O Ajustar pH usando NaOH a 7.4. Calcular la osmolaridad y completar los 400 mOsm con NaCl Completar los dos litros UA Biop...")
14:00, 31 May 2023 ‎UA Biophysics:Protocols:Calcein ESP (hist | edit) ‎[1,249 bytes] ‎Elizabeth Suesca (talk | contribs) (Created page with "'''Calceina: 400 mOsM, 50 mM, 100 ml, pH 7.4 ''' ==Materiales: == * Probeta 100 ml * 30 ml de NaOH (1M) * HCl (1M) * 3,113 g de calceina * 40 ml Buffer H: ** 5 ml de EDTA 0.2 mM (Para que quede a 0.01 mM en la solución final) ** HEPES 238.3 mg (para que quede a 10 mM en la solución final). ==Procedimiento: == # En la probeta medir 20 ml de NaOH 1M y colocar agitador # Disolver en el NaOH 3,113 g de calceina # Agregar los 40 ml del Buffer H a la calceina # A...")
08:31, 31 May 2023 ‎UA Biophysics:Protocols:Bacteria for Lipid Extraction ESP (hist | edit) ‎[1,206 bytes] ‎Elizabeth Suesca (talk | contribs) (Created page with "==Materiales para 1.4 g de célula== * Plato con SA401, máximo de un mes desde la recuperación * Frasco de vidrio con 10 ml de LB * 2 L de LB repartidos en 13 Erlenmeyer de 500 ml ==Procedimiento== '''Dia 1''' 4:00 pm ON de SA401: una colonia en el frasco con 10 ml de LB. '''Dia 2''' 8:30 am Dilución de las células: 10 ul en cada Erlenmeyer '''Dia 3''' 8:30 am Concentrar la muestra * Prepara la centrífuga a 4°C. * Refrigerar lo...")
12:57, 29 May 2023 ‎UA Biophysics:Protocols:Bacteria for Lipid Extraction (hist | edit) ‎[431 bytes] ‎Elizabeth Suesca (talk | contribs) (Created page with "==Materiales para 1.4 g de célula== * Plato con SA401, máximo de un mes desde la recuperación * Frasco de vidrio con 10 ml de LB * 2 L de LB repartidos en 13 Erlenmeyer de 500 ml ==Procedimiento== '''Dia 1''' 4:00 pm ON de SA401: una colonia en el frasco con 10 ml de LB. '''Dia 2''' 8:30 am Dilución de las células: 10 ul en cada Erlenmeyer '''Dia 3''' 8:30 am Concentrar la muestra * Prepara la centrífuga a 4°C. * Refrigerar lo...")
12:17, 29 May 2023 ‎UA Biophysics:Protocols:Erythromycin (hist | edit) ‎[1,230 bytes] ‎Elizabeth Suesca (talk | contribs) (Created page with "Erythromycin has been used as a motilin receptor agonist, to block respiratory glycoconjugate secretion in human airways in vitro, and for selecting plasmid-cured and recombinant lactococcus lactis MG1363 strains. ==STOCK SOLUTION== Erythromycin is used in the biophysics lab at a 2 ug/ml. Stock solutions are at 1 mg/mL ==PROTOCOL (STORAGE)== According to desired amount of antibiotics, calculate the amount in grams that has to be weighed. For example, for 20mL of 25mg...")
11:58, 29 May 2023 ‎UA Biophysics:Protocols:Calcein (hist | edit) ‎[109 bytes] ‎Elizabeth Suesca (talk | contribs) (Created page with "Receta para 100 ml, 50mM, 400 mOsM, pH 7,4 Materiales: Probeta 100 ml 30 ml de NaOH 3,113 g de calceina Procedimiento: En probeta 20 ml de NaOH 1M (colocque 21 ml) Disolver en el NaOH 3,113 g de calceina Mezclar 5 ml de EDTA 0.2 mM (Para que quede a 0.01 mM en la solución final) y HEPES 238.3 mg (para que quede a 10 mM).completar un volumen de 40 ml Agregar la mezcla a la calceina Ajustar pH con HCl 1M (2 ml) Entre HCl y NaOH se agregaron 2...")
16:34, 24 May 2023 ‎UA Biophysics:SysBio Meeting:2023-I Meetings (hist | edit) ‎[2,632 bytes] ‎Jd.marmolejol (talk | contribs) (Created page with "Stability of two competing populations in chemostat where one of the population changes its average mass of division in response to changes of its population - https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0213518 Dynamical Model of Drug Accumulation in Bacteria: Sensitivity Analysis and Experimentally Testable Predictions - https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0165899 Transcription factor specificity limits the number...")
02:24, 24 May 2023 ‎RNA samples purification (hist | edit) ‎[297 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "==Materials== * DNAse ==Protocols== * Protocol for RNA Cleanup and Concentration Using A&A Biotechnology kit [https://www.dropbox.com/s/ircnq2d06odfrog/Clean-Up-RNA-Concentrator-EN.pdf?dl=0] ==DNA purification form== [https://www.dropbox.com/s/szmyicqx8f3xlt3/RNA clean up.xlsx?dl=0]")
15:47, 23 May 2023 ‎Schumer lab: Data currently available on Oak (hist | edit) ‎[294 bytes] ‎Schumer (talk | contribs) (Created page with "==Data currently available on Oak=== We keep an up-to-date log of data currently available on Oak in the following google sheet. If you download any raw data, please make sure to update it! https://docs.google.com/spreadsheets/d/1dUBAmaz2bNa-LppWxFZ7Vymld-jxrDbh-HC_WFjXSzA/edit#gid=89601434")
16:38, 22 May 2023 ‎Schumer lab: Swordtail Dropbox quick guide (hist | edit) ‎[619 bytes] ‎Schumer (talk | contribs) (Created page with "==Swordtail Dropbox== Dropbox is home to the most important documents in the lab that aren't raw data. For ease of access, I am also linking some commonly used documents here: *Lab manual *New lab member checklist *Site codes and information *")
15:42, 22 May 2023 ‎Schumer lab: Shared resources (hist | edit) ‎[925 bytes] ‎Schumer (talk | contribs) (Created page with "==Introduction== Many people in the lab use the same shared resources and contribute to developing these resources. Resource files such as genome assemblies, annotation files, recombination maps, and files for ancestry inference can all be found in: /home/groups/schumer/shared_bin/shared_resources ===Current resources map=== This google document describes the most commonly used resources in shared_resources and provides useful info...")
10:06, 22 May 2023 ‎McClean:EMSA Protocol (hist | edit) ‎[8,975 bytes] ‎Rjszakaly (talk | contribs) (Created page with "==Overview== This is a protocol for the LightShift Chemiluminescent EMSA Kit from Thermo Scientific (cat # 20148).")
10:04, 22 May 2023 ‎Microfluidic Detection Methods- Diana Barr, Emma Abi-Younes, Xiao Fan, Jason Kim, Ryan Lodge, Nick Uvanovic, Xiaoyu Zhang (hist | edit) ‎[21,543 bytes] ‎DeBarr (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} == Introduction: Microfluidic Detection Methods == Detections, done through sensors, encompass a variety of technologies that, in response to changes that occur, produce signals sent to a transducer to convey information about a system. Sensors typically consist of three major components which include electrical circuits, a conversion element, and a sensing element. Microfluidics has allowed for microfluidic sensing to make an impact in these...")
17:21, 16 May 2023 ‎SIMPLE paper pumps - Raymond Pho (hist | edit) ‎[6,652 bytes] ‎Raymondpho (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} =General Overview= Self-powered Imbibing Microfluidic Pump by Liquid Encapsulation (SIMPLE) is a microfluidic platform that was developed by MeBioS groups at KU Leuven, Belgium. This platform aims to address the need for cost efficient, robust, easy to use, and autonomous for point of care (POC) devices. SIMPLE mainly utilizes difference in pressure from one end of the device to the other to drive fluid flow within the microchannel structure...")
04:53, 16 May 2023 ‎Manual protocol (hist | edit) ‎[1,698 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with " מאמר 1 dx.doi.org/10.17504/protocols.io.2yfgftn אנא זכרו לצטט עם הפרוטוקול- https://www.ncbi.nlm.nih.gov/pubmed/28856640 ציטוט פרוטוקול- Benjamin Schwessinger 2019. High quality DNA from Fungi for long read sequencing e.g. PacBio. protocols.iohttps://dx.doi.org/10.17504/protocols.io.2yfgftn הפקת DNA באיכות גבוה לרצף PacBio מותאם להפקת DNA מנבגי חלודה מחיטה ומשעורה. הכי...")
04:52, 16 May 2023 ‎QiaGen's kit protocol (hist | edit) ‎[15,732 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "מידע מהhandbook: הקיט מיועד לבידוד DNA כרומוזומלי בגדול של 20-150 kb (איור 1 עמוד 8) מתוך עמוד 13- הקיט מכיל בופרים שממיסים את מרכיבי התא, הכל קורה על גבי המסננת של הטיפ 20/G שעשוי שרף וקושר את הDNA בתנאי מלח וPH מתאימים, לכן יש להימנע מייבוש המסננת. חלבונים וזיהומים בעלי משקל...")
04:49, 16 May 2023 ‎DNA extraction for genome sequencing (hist | edit) ‎[53 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "==Manual protocol== ==QiaGen's kit protocol==")
04:44, 16 May 2023 ‎DNA samples purification (hist | edit) ‎[492 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "==Protocols== * Protocol for DNA Cleanup and Concentration Using the Monarch [https://www.dropbox.com/s/fh441z99va5h54y/Monarch_PCRDNA_Cleanup.pdf?dl=0] * Wizard® SV Gel and PCR Clean-Up System [https://www.dropbox.com/s/0iekonqwxtny5np/Wizard SV Gel and PCR Clean-up System Quick Protocol FB072.pdf?dl=0]")
10:44, 13 May 2023 ‎Extraction of RNA (hist | edit) ‎[329 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "===Safety measures=== * '''After adding the chloroform, the work should be conducted in the chemical hood''' ==RNA extraction protocol== * Hybrid-R [https://www.dropbox.com/s/6s5yniyuq3sfrmu/Hybrid-R protocol.pdf?dl=0] ==RNA extraction form== * [https://www.dropbox.com/s/6s5yniyuq3sfrmu/Hybrid-R protocol.pdf?dl=0]")
21:30, 10 May 2023 ‎Amino acids composition (hist | edit) ‎[567 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "* The samples should be freeze-dried (4-10 mg of dried sample) * An account should be open at the Research Core Facilities Program at UC Davis [https://ppms.us/ucdavis/login/?pf=8] * Please print out this e-mail and include it with your samples. If you have a IOC/Recharge # (UC) or a PO # please note, or if you would rather be invoiced (and pay by credit card) please indicate here Please do not hesitate to call (530-752-7327 ) or e-mail (msf@ucdavis.edu) if you h...")
22:19, 8 May 2023 ‎Extraction of DNA (hist | edit) ‎[396 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "==Protocols of extraction kits== * QiaGen")
11:49, 8 May 2023 ‎McClean:Spectinomycin (hist | edit) ‎[1,458 bytes] ‎Rjszakaly (talk | contribs) (Created page with "==Overview== Protocol for making 20mL of 100mg/mL Spectinomycin stock solution ==Materials== # sterile De-Ionized Water # Spectinomycin # 0.22um syringe filter # 30ml syringe # sterile 1.5ml eppie tubes ==Procedure== * Fill a 50mL centrifuge tube with 20mL of sterile, DI water. * Weigh out 2g Spectinomycin. Insert this into the tube. * Vortex the tube vigorously until it is well-mixed. * Filter sterilize the solution by pushing through a 0.22um syringe filter. * Aliquo...")
11:27, 8 May 2023 ‎McClean:Hygromycin B (hist | edit) ‎[1,535 bytes] ‎Rjszakaly (talk | contribs) (Created page with " Stock is 50 mg/mL (166X) Final concentration 300 ug/mL Use 6ul of stock per ml of media")
11:21, 8 May 2023 ‎McClean:ClonNat (hist | edit) ‎[1,508 bytes] ‎Rjszakaly (talk | contribs) (Created page with "==Overview== Protocol for making 20mL of 50mg/mL ClonNat stock solution ==Materials== # sterile De-Ionized Water # ClonNat # 0.22um syringe filter # 30ml syringe # sterile 1.5ml eppie tubes ==Procedure== * Fill a 50mL centrifuge tube with 20mL of sterile, DI water. * Weigh out 1g ClonNat. Insert this into the tube. * Vortex the tube vigorously until it is well-mixed. * Filter sterilize the solution by pushing through a 0.22um syringe filter. * Aliquot 1ml of the soluti...")
11:02, 8 May 2023 ‎McClean:Gentamicin (hist | edit) ‎[1,449 bytes] ‎Rjszakaly (talk | contribs) (Protocol for making the 50mg/ml stock solution of Gentamicin)
06:13, 3 May 2023 ‎Sample preparation for LCMS (hist | edit) ‎[5,175 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "# 10 BSF larvae from each replicate and treatment should ground with liquid nitrogen. 2. The larval powder should be freezed immediately in -80°C until lyophilization. 3. After lyophilization, 100 mg of larval powder dissolved in 700 microliters of precooled metabolite extraction buffer (80% methanol and 0.1% formic acid), resuspended by vortex, incubated on ice for 5 min at 4 °C. (Metabolite extraction buffer: To prepare working stock for 50 ml of extraction buffer,...")
06:09, 3 May 2023 ‎Sample dilution (hist | edit) ‎[573 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "===Equipment=== * Brown veils and cups * Inserts ===Materials=== * benzophenone * Petroleum ether ==Protocol== ===Solutions A=== For 30 ml - 29.7 ml petroleum ether + 300 ul benzophenone ===Solution B=== For 30 ml - 25 ml '''solution A''' + 25 ml petroleum ether ===Sample dilution=== * Each sample should be diluted to two concentrations: 1:125 and 1:5000 * From each sample 8 ul will be dilutes with 992 ul '''solution B''' (for 1:125 dilution) * From each sample 25 ul...")
05:56, 3 May 2023 ‎Calibration curve (hist | edit) ‎[873 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "===Equipment=== * Brown veils and cups * Inserts ===Materials=== * benzophenone * Petroleum ether ==Protocol== ===Solutions A=== for 30 ml - 29.7 ml petroleum ether + 300 ul benzophenone ===Solution B===")
05:51, 2 May 2023 ‎Fatty acids composition (hist | edit) ‎[1,449 bytes] ‎Insect Nutrition and Metabolism (talk | contribs) (Created page with "===Safety measures=== * '''When preparing the Sulfuric acid - to do it the chemical hood (with lowered glass) with safety glasses and thick gloves''' * '''Pour the acid into the methanol in cooled (with ice) bucket''' * '''The work should be conducted in chemical hood''' * '''When dealing with hot equipment and sulfuric acid - wear thick gloves''' ===Equipment=== * '''before working with the Gooch make sure the clean them in the dish washer, burn them in 600 degrees an...")
14:48, 29 April 2023 ‎Octobots (hist | edit) ‎[4,864 bytes] ‎Joebijujosep (talk | contribs) (Created page with "The Octobot is a 3-D printed, fully autonomous microfluidic robot. The robot is made completely out of soft materials such as polydimethylsiloxane (PDMS) and Pluronic F127, SE 1700, and Sylgard 184, which are soft, silicone-based materials. In place of a rigid control center, the octobot is powered by a microfluidic logic circuit alongside a decomposition reaction that generates gas <ref name="Michael" /> Several different fabrication techniques are used to produce the...")
13:49, 28 April 2023 ‎3D Paper Microfluidics - Peiyao Zhao, Adaline Nuesse, Lucas Rozanski (hist | edit) ‎[26,636 bytes] ‎Rfan (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} =Introduction= As a core of point-of-care diagnostics, microfluidics paper-based analytical devices(μPADs) are crucial for preventing the spread of infectious diseases and the improvement of global healthcare through more affordability and feasibility to be implemented in remote locations and developing regions. Current μPADs are low cost, require small amounts of sample volume and can be used easily without requiring intense training and s...") originally created as "3D Microfluidics Paper-based Analytical Device - Peiyao Zhao, Adaline Nuesse, Lucas Rozanski"
09:41, 28 April 2023 ‎3D microfluidics paper-based analytical device - Peiyao Zhao, Adaline Nuesse, Lucas Rozanski (hist | edit) ‎[26,610 bytes] ‎Rfan (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} ==Introduction and Motivation== 175px|thumb|upright=1.5|Fig. 1. Manufacturing of multilayered paper microfluidic device using tape to adhere between layers.[[https://doi.org/10.1073/pnas.0810903105 1 Martinez, A. W., Phillips, S. T., & Whitesides, G. M. Three-dimensional microfluidic devices fabricated in layered paper and tape. Proceedings of the National Academy of Sciences 2008. Cop...")
13:00, 26 April 2023 ‎Micromolding in Capillaries (MIMIC) - Wen-Wei Wong (hist | edit) ‎[11,548 bytes] ‎Wwwong (talk | contribs) (Created page with "mimic")
13:14, 19 April 2023 ‎3D Cell Culture - McLean Taggart, Emma Villares, Maximillian Marek, Scott LeBlanc, and Adam Lyons (hist | edit) ‎[18,717 bytes] ‎Sleblanc (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}}")
18:41, 17 April 2023 ‎Microfluidic Sensing- Diana Barr, Emma Abi-Younes, Xiao Fan, Jason Kim, Ryan Lodge, Nick Uvanovic, Xiaoyu Zhang (hist | edit) ‎[18,728 bytes] ‎DeBarr (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} == Introduction: Microfluidic Sensing == Sensors encompass a variety of technologies that, in response to changes that occur, produce signals sent to a transducer to convey information about a system. Sensors typically consist of three major components which include electrical circuits, conversion element, and a sensing element. Microfluidics has allowed for microfluidic sensing to make an impact in these technologies with a range of applicati...")
12:23, 17 April 2023 ‎Microfluidic Sensing- Diana Barr (hist | edit) ‎[15,928 bytes] ‎DeBarr (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}}")
18:34, 16 April 2023 ‎"Pick and Place" Assembly of Parts Using PDMS - Amy Lim (hist | edit) ‎[14,382 bytes] ‎Amylim (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} =What is PDMS? = thumb|Fig. 1 Chemical Structure of Polydimethylsiloxane.[https://www.acs.org/molecule-of-the-week/archive/p/polydimethylsiloxane.html [1] ] Polydimethylsiloxane (PDMS) is a silicone elastomer, being the simplest kind of silicone polymer at that. https://www.acs.org/molecule-of-the-week/archive/p/polydimethylsiloxane.html 1 PDMS is made up of a monomer and cross...")
18:28, 16 April 2023 ‎Microfluidic Sensing- Liquid Metal Sensors - Jason Kim (hist | edit) ‎[11,874 bytes] ‎Jasonkim (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} =Liquid Metal Sensors= Liquid metal sensors are sensors that utilize liquid metal in their circuits. Typically liquid metal is used for properties such as flexibility, ability to be stretched, ease of application and various other magnetic, thermal, or electrochemical properties. https://pubs.acs.org/doi/10.1021/acssensors.1c02606 1 Typical sensors use solid metal in their circuits and so have limited geometry as well as a static...")
18:26, 16 April 2023 ‎Microfluidic Gradient Generators - Greg Schneider (hist | edit) ‎[10,334 bytes] ‎Gjschneider (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} = Nonlinear Gradients = In order to generate solutions which do not mix linearly along a concentration gradient, nonlinear (e.g., exponential, logarithmic, or sigmoidal) mixing gradients can be creating using microfluidic mixing techniques. This is primarily achieved by varying fluid channel length or by designing asymmetrical microfluidic channels. As opposed to traditional gradient generation devices, such as Microwell plates, the gradient ac...") originally created as "Gradients - Greg Schneider"
16:49, 16 April 2023 ‎SIMPLE paper pumps (KU Leuven) - Raymond Pho (hist | edit) ‎[5,501 bytes] ‎Raymondpho (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} =General Overview=")
13:26, 16 April 2023 ‎"Pick and Place" assembly of parts using PDMS - Amy Lim (hist | edit) ‎[11,101 bytes] ‎Amylim (talk | contribs) (Created blank page)
13:24, 16 April 2023 ‎Applications of 3D Printing (hist | edit) ‎[8,334 bytes] ‎Joebijujosep (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} ==Tissue Engineering== Let's say Mike Tyson bit off more then just a chunk of your ear. 3D bioprinting has the potential to customize a new ear for you. {{clear}} Image:LukeRuks5.png|thumb|left|780px|A 3D bioprinting system (a) The ITOP system consists of three major units: (i) 3-axis stage/controller, (ii) dispensing module including multi-cartridge and pneumatic pressure controller and (iii) a closed acrylic chamber with temperature contro...")
10:49, 16 April 2023 ‎Common 3D Printing Materials (hist | edit) ‎[7,559 bytes] ‎Joebijujosep (talk | contribs) (Created page with "==Polydimethylsiloxane (PDMS)== 3D printing is widely used to print polydimethylsiloxane ('''PDMS''') based microfluidic devices. 3D rapid prototyping fabrication technique maintains the desirable permeability and bio-compatibility of PDMS. The ink for 3D printing PDMS can be prepared by blending a shear thinning PDMS material, and a low-viscosity PDMS material. After desired mixing, the final PDMS inks were loaded into a syringe barrel at room temperature. Using a 3D bi...")
08:59, 16 April 2023 ‎Nonlinear Gradients - Greg Schneider (hist | edit) ‎[4,478 bytes] ‎Gjschneider (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} = Background = In order to generate solutions which do not mix completely, nonlinear (e.g., exponential, logarithmic, or sigmoidal) mixing gradients can be creating using microfluidic mixing techniques. This is primarily achieved using asymmetrical microfluidic channel designs, or channels of varying length. As opposed to traditional gradient generation devices, such as Microwell plates, the gradient across a microfluidic device can be quantifi...")
08:38, 16 April 2023 ‎Types of 3D Printing (hist | edit) ‎[13,484 bytes] ‎Joebijujosep (talk | contribs) (Created page with "==Types of Printing== There are many different technologies to do 3D printing. Since 2010, the American Society for Testing and Materials ('''ASTM''') carried out the “ASTM F42 – Additive Manufacturing” standards[2]. Those standards are used to classify the additive manufacturing processes into 7 categories[2]. Those 7 categories are[2] [https://3dprinting.com/what-is-3d-printing/]: # Vat Photopolymerisation ##Stereolithograph...")
08:37, 16 April 2023 ‎3D Printing Overview (hist | edit) ‎[5,987 bytes] ‎Joebijujosep (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} ==Terminology== thumb|right|250px|Figure 1: CAD image of a teacup; additional rendering shows differences in final build due to differences in layer thicknesses<ref name="gibson" /> 3D printing is the colloquial term for the rapid prototyping process formally known as additive manufacturing or rapid prototyping<ref name="gibson">Gibson, I., Rosen, D. & Stucker, B. Additive Manufacturing Technology. in Additive Man...")
17:26, 15 April 2023 ‎Gradient Trees - Greg Schneider (hist | edit) ‎[10,845 bytes] ‎Gjschneider (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} = Paperfuge Background = 300px|right|thumb|'''Figure 1''' Paperfuge being pulled to rapidly spin. Note the supercoiling as the string winds up. Reproduced with permission. Copyright 2017 Nature Biomedical Engineering.[[https://doi.org/10.1038/s41551-016-0009 1]] A paperfuge (“paper-centrifuge”) is a portable, inexpensive, human-powered centrifuge designed by Manu Prakash and his team at Stanford Univers...")
19:47, 12 April 2023 ‎3D Printing - Joe (hist | edit) ‎[6,151 bytes] ‎Joebijujosep (talk | contribs) (Created page with "{{Template:CHEM-ENG590E}} ==Terminology== thumb|right|250px|Figure 1: CAD image of a teacup; additional rendering shows differences in final build due to differences in layer thicknesses<ref name="gibson" /> 3D printing is the colloquial term for the rapid prototyping process formally known as additive manufacturing or rapid prototyping<ref name="gibson">Gibson, I., Rosen, D. & Stucker, B. Additive Manufacturing Technology. in Additive Man...")
05:08, 28 March 2023 ‎BioMicroCenter:News2017+ (hist | edit) ‎[7,710 bytes] ‎Stuart S. Levine (talk | contribs) (Created page with "{{BioMicroCenter}} ===MARCH 2020=== The MIT BioMicro Center is pleased to announce the addition of the NovaSeq 6000 to its wide range of Illumina Sequencing Instruments. The NovaSeq 6000 uses patterned flow cell technology and is capable of delivering up to 10 billion reads per run, and is promising for high-throughput single-cell sequencing, exome sequencing, and applications that can benefit from high coverage. === JULY 2017 === We have several exciting developm...")

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