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Norland optical adhesive 81

Manufactured by Norland Products
Sourced in United States

Norland Optical Adhesive 81 is a single-component, ultraviolet-curable adhesive. It is designed for bonding various materials, including glass, metals, and plastics. The adhesive cures upon exposure to ultraviolet light, forming a strong, durable bond.

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4 protocols using norland optical adhesive 81

1

Fabrication of Colloidal Silicon Nitride AFM Probes

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Custom colloidal silicon nitride AFM probes were constructed from tipless AFM cantilevers (spring constant 0.08 N/m; NanoAndMore USA, Soquel, CA, USA). Borosilicate microspheres (5.20 µm in diameter; Bangs Laboratories, Fishers, IN, USA) were attached near the free end of the AFM cantilever with Norland optical adhesive #81 (Norland Products, Cranbury, NJ, USA). The spherical probe serves as a model of a single asperity and as such the contact area during sliding is known (Coles et al. 2008 (link)). To ensure uniformity, cantilevers were coated with 40 nm of gold over a 5-nm adhesion layer of chromium in a thermal evaporator. The mounted probe was submerged in PBS for at least 20 min prior to imaging to allow for thermal equilibration at room temperature.
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2

Covalent Antibody Immobilization on AFM Beads

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6.1 µm carboxylate beads (Polysciences, Inc, USA) were dried on a cleaned coverslip coated in tetra-chlorosilane (Gilest, USA). Using the AFM head manual z translation stage (Asylum Research MFP3D, Oxford Instruments, UK), a tipless cantilever (Nanoworld TL1-Arrow-50; Nanoworld, Switzerland) was lowered onto a droplet of UV polymerizing glue (Norland optical adhesive 81; Norland Products, USA) on the same coverslip. The cantilever was lowered onto a suitable bead and a UV flashlight was used to slightly cure the glue before raising the beaded cantilever off the surface of the coverslip. The entire chip was placed under a UV lamp for 5 minutes to cure the glue completely.
The beaded cantilever was then placed in the chip holder and onto the AFM head. The tip was then dipped into a series of four droplets on a UV-cleaned coverslip: (1) a droplet of 10 mg/mL EDAC (1-ethyl-3-(-3-dimethylaminopropyl) carbodimide; Fisher Scientific) in PBS for 2 min; (2) PBS, 2 min; (3) 33 ug/mL Goat anti-Mouse IgG-AlexaFluor488 (ab150113, Abcam) for 5 min; (4) PBS, >2 min and submerged until used. IgG was centrifuged for 5 min at 10,000 g before use in functionalization steps.
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3

Hydrogel Fabrication in Custom Chambers

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Hydrogels were made in custom sample chambers in a glass-bottomed Petri dish (d = 35 mm, no. 1.5 glass coverslip, MatTek Corporation). A polydimethylsiloxane (PDMS, Sylgard) cylindrical chamber with a 10 mm outer diameter and 8 mm inner diameter was made using biopsy punches (Integra Biosciences). The PDMS chamber was then loosely attached to the bottom of the glass-bottomed Petri dish using ultraviolet (UV) curing adhesive (Norland Optical Adhesive 81, Norland Products Inc.), which was cured with UV light at 365 nm for 3 min. This adhesive allows for sufficient attachment to the Petri dish but also allows for removal of the PDMS chamber. The PDMS chamber was used to hold the polymer precursor solution during the gelation process and was removed following gelation to enable equal swelling (in growth medium) in the axial and radial directions.
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4

Norland Optical Adhesive 81 Protocol

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Norland Optical Adhesive 81 (NOA81) was purchased from Norland Products (Cranbury, NJ, USA), and used as received. This adhesive was reported as a mixture of mercapto-esters (50–70 wt %) and triallyl isocyanurate (30–50 wt %). Perfluoromethyldecalin (85% pure) was purchased from ABCR (Karlsruhe, Germany), acetone (99.8% pure) was purchased from Daejung (Seoul, South Korea), and polyethylene glycol (PEG) with an average molecular weight of 4000 g/mol was purchased from Fisher Chemical (Loughborough, England). All of the chemicals were used without further purification. De-ionized water (~18 MΩ) was provided from an inhouse source.
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