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Anti human tnf α antibody

Manufactured by Thermo Fisher Scientific

The Anti-human TNF-α antibody is a laboratory reagent used to detect and quantify the presence of human tumor necrosis factor alpha (TNF-α) in biological samples. TNF-α is a key inflammatory cytokine involved in various physiological and pathological processes. This antibody can be utilized in techniques such as ELISA, Western blotting, and immunohistochemistry to measure TNF-α levels in research applications.

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2 protocols using anti human tnf α antibody

1

Functionalizing MoS2 Transistor Sensor for TNF-α Detection

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Figure S1 in the supporting information illustrates the protocol for functionalizing the HfO2 effective layer of a MoS2 transistor sensor with anti-human TNF-α antibody receptors for detecting TNF-α molecules. First, an as-fabricated transistor biosensor is immersed in 5% (3-Aminopropyl) triethoxysilane (APTES, purchased from Sigma-Aldrich Co. LLC.) in ethanol for 1 hour. After the incubation, the sensor is rinsed with phosphate buffered saline (PBS) and blown dry by nitrogen gas. After this step, the HfO2 effective layer is silanized with an APTES monolayer. The device is subsequently immersed in 5% gluteraldehyde (GA) (purchased from Sigma-Aldrich Co. LLC.) in PBS for 2 hours followed by rinsing with PBS. Afterwards, anti-human TNF-α antibody (from eBioscience, Inc.) of 50 ug/ml concentration in DI water is dropped on the sensor and incubated for 1 hour. For studying the equilibrium-state sensor responses, the as-functionalized sensor is incubated with TNF-α solutions with incremental concentrations (i.e., n = 60 fM, 300 fM, 600 fM, 3 pM, and 6 pM; the incubation time for each of the concentrations: ~2 hours). The incubation is performed using the setup illustrated in Fig. 1(d). After each incubation process, the transfer characteristics of the transistor sensor are measured.
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2

Sensitive Multiplex Antigen Detection

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Monoplex devices were incubated with solutions containing 50 pg/mL-500 ng/mL of the target antigen (human TNF-α). Likewise, multiplex devices were incubated with solutions containing 10 pg/mL-100 ng/mL of the target antigen (mouse IL-1α). The multiplex devices also incorporated positive control (biotinylated antibody, eBioscience #13-7349) and negative control (anti-human TNF-α antibody, eBioscience #14-7348) microneedles. Signals were detected using the blotting technique. Device sensitivity was expressed as the lowest antigen concentration that produced a signal.
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