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Anti fgf21

Manufactured by Cell Signaling Technology
Sourced in United States

Anti‐FGF21 is a laboratory reagent used to detect and analyze the fibroblast growth factor 21 (FGF21) protein. FGF21 is a metabolic regulator involved in glucose and lipid homeostasis. Anti‐FGF21 can be used in various research applications such as Western blot, ELISA, and immunohistochemistry to study the expression and function of FGF21 in biological samples.

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2 protocols using anti fgf21

1

Western Blot Analysis of FGF21 Protein

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Protein samples were prepared by homogenising frozen tissue samples in RIPA buffer (Thermo Fisher®) supplemented with SIGMA FAST® EDTA‐free protease inhibitor cocktail (Sigma®). Protein concentrations were determined via the Pierce BCA Protein Assay Kit (Thermo Fisher®), and 20 μg of each sample was run on a 4%‐ to 20%‐gradient polyacrylamide gel (BioRad®). Standard western blotting protocols were followed utilising nitrocellulose membrane (BioRad®). Primary antibodies were obtained from Invitrogen® (Anti‐FGF21; MA 5–35418) and Cell Signaling® (Anti‐Beta Actin; 4970). The anti‐rabbit IgG DyLight™ 800 (Cell Signaling®; 5151) was used as the secondary antibody, and blots were scanned with the LiCor Odyssey® infrared scanner. The Odyssey software was utilised for detection and band intensity calculations. Signal intensities of FGF21 were determined relative to those of beta actin.
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2

Western Blot Analysis of Adipose and Liver Proteins

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Western blots of proteins in the adipose and liver were performed as previously described (Berg & Scherer, 2005 (link); Collins et al., 2016 (link); Hotamisligil, 2006 (link)). Primary antibodies for anti-NOV/CCN3, anti-IL-6, anti-pP65, anti-P65, anti-MMP9, anti-MMP2, anti-MT1-MMP, anti-TIMP1, anti-TIMP2, anti-PRDM16, anti-PGC-1α, anti-SOD1, anti-TWIST1, anti-SIRT1, anti-Mfn1, anti-FGF21, anti-CREG1, anti-UCP1, anti-pAKT, anti-AKT, and anti-β-actin were purchased from Cell Signaling Technology, Danvers, MA, USA. The anti-pIR tyr972 antibody was purchased from Millipore, Bedford, MA, USA. The anti-HO-1 antibody was purchased from Enzo Life Sciences, Farmingdale, NY, USA. The secondary antibodies labeled with either IRDye 680 or IRDye 800 were purchased from LICOR Biosciences, Lincoln, NE. Immunoreactivity was visualized and quantified by infrared scanning in the Odyssey system (LICOR Biosciences, Lincoln, NE) and quantified after normalization with β-actin and expressed as arbitrary units (AU).
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