The largest database of trusted experimental protocols

Su 8 2050 negative photoresist

Manufactured by MicroChem
Sourced in United States

SU-8 2050 is a negative photoresist designed for microelectronic applications. It is a high contrast, epoxy-based photoresist suitable for micromachining and other microelectronic applications. The product is formulated to provide excellent chemical and thermal stability.

Automatically generated - may contain errors

4 protocols using su 8 2050 negative photoresist

1

Micro Electroforming Mold Fabrication

Check if the same lab product or an alternative is used in the 5 most similar protocols
In this paper, SU-8 2050 negative photoresist and propylene glycol methyl ether acetate (PGMEA, 1-methoxy-2-propanol acetate) developer (MicroChem Corp., Westborough, MA, USA) were used to prepare the micro electroforming mold. Polished 1 mm thick stainless steel (1Cr18Ni9Ti) sheet was employed as the substrate. An n-methyl pyrrolidinone solution was used to remove the cross-linked SU-8 structure after micro electroforming. The structures and roughness were examined using a confocal laser scanning microscope (CSLM, Olympus LEXT OLS4000, Olympus Corporation, Tokyo, Japan).
+ Open protocol
+ Expand
2

Fabrication of Microfluidic Device Layers

Check if the same lab product or an alternative is used in the 5 most similar protocols
The entire microfluidic device consists of three layers: the sample layer, the buffer layer, and the top microchannel layer. The sample layer and buffer layer were fabricated by molding processed polymethyl methacrylate (PMMA) templates. The microchannels were fabricated by standard photolithography techniques [38 (link)]. The patterns of the chip were designed using AutoCAD 2022 (Autodesk, San Francisco, CA, USA), and SU-8 2050 negative photoresist (Microchem, Newton, MA, USA) was spin-coated onto the pretreated silicon wafer to create a 40 μm high photoresist layer. After spin coating, the baked wafer was exposed to 365 nm UV. The patterned wafer was baked again and developed using a SU-8 developer (Microchem). The polydimethylsiloxane (PDMS, Dow Corning Sylgard 184) was mixed with a curing agent at a 10:1 ratio, poured onto the PMMA templates and patterned wafer, and cured at 80 °C for 2 h. The cured PDMS replicas were peeled off. A puncher with a 1.00 mm inner diameter was used to punch inlet holes for the microchannel of the PDMS device. After plasma treatment, the cured PDMS chips were brought into contact and heated in an oven at 80 °C to achieve an irreversible bonding. For more details see Supplementary Materials (Figure S1).
+ Open protocol
+ Expand
3

Microfabrication and Biofilm Staining

Check if the same lab product or an alternative is used in the 5 most similar protocols
Luria Bertani (LB) broth are composed of 0.5% yeast extract, 1% peptone, 1% NaCl and deionized water, all of which were purchased from Beijing Ao Xing Bio-tech (Beijing, China). Ethanol and amoxicillin were obtained from Sigma-Aldrich (Shanghai, China). SU-8 2050 negative photoresist was purchased from Micro Chem Corp. (Newton, MA, USA). Polydimethylsiloxane (PDMS) Sylgard 184 was obtained from Dow Corning (Midland, MI, USA). Borosilicate glass was achieved from Matsunami (Kyoto, Japan). FilmTracer TM SYPRO® Ruby Biofilm Matrix Stain was purchased from Invitrogen (Waltham, MA, USA).
+ Open protocol
+ Expand
4

Fabrication of PDMS Microchip for Cell Culture

Check if the same lab product or an alternative is used in the 5 most similar protocols
The PDMS microchip was designed in AutoCAD software and fabricated using standard soft lithography fabrication technology.[23] SU‐8 2050 negative photoresist (MicroChem) was used to fabricate 40 µm thick micropillars and 100 µm thick micropattern on silicon wafers. A closed microchannel on the top layer had 1 mm width, 100 µm depth, and 10 mm length. The wafers were then treated with tridecafluoro‐(1,1,2,2‐tetrahydrooctyl)‐1‐trichlorosilane saline (Sigma‐Aldrich). Next, PDMS (10A: 1B; Dow Coring) was poured onto the photoresist masters and heated at 70 °C for 1 h to achieve a fully cross‐linked PDMS replica‐molded. The two pieces of PDMS were peeled off, holes punched, and plasma bonded irreversibly (Harrick Plasma, PDC‐32G) to form the microfluidic chip. It is believed that the microchip would be suitable for long‐term cell culture with high viability due to biocompatible PDMS material.[49, 50]
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!