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Mouse anti rtfdc1 antibody clone 1e8

Manufactured by LifeSpan BioSciences

The Mouse anti-RTFDC1 antibody (clone 1E8) is a laboratory tool designed for the detection and study of the RTFDC1 protein. It is a monoclonal antibody produced in mice and can be used in various immunoassay techniques.

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2 protocols using mouse anti rtfdc1 antibody clone 1e8

1

Antibody Panel for Influenza and Immune Proteins

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The following antibodies were used: from EMD Millipore, anti-influenza A virus HA (1:200; catalog number AB1074); from Abcam, anti-IFITM1 (1:2,000; catalog number ab224063) and mouse anti-β-actin antibody (1:15,000; catalog number ab6276); from Thermo Fisher, Alexa Fluor 488-conjugated donkey anti-goat IgG (1:500; catalog number A11055), a rabbit anti-mouse IgG (H+L) secondary antibody Alexa Fluor 488 conjugate (1:500; catalog number A-11059), and mouse anti-alpha-tubulin antibody (1:2,000; clone DM1A; catalog number 14-4502-82); from Cell Signaling Technology, anti-IFITM3 (1:2,000; catalog number 59212T), anti-STING (1:2,000; catalog number 13647), anti-pSTAT1 (1:2,000; clone Y701; catalog number 9167), and anti-TATA-binding protein (1:2,000; catalog number 8515s); and from LifeSpan Biosciences, mouse anti-RTFDC1 antibody (clone 1E8; 1:2,000; catalog number LS-C340588).
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2

Cell Fractionation and Protein Analysis

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The cell fractionation protocol was adapted from the Ficoll-digitonin protocol previously described (44 (link)). Briefly, 1.5 × 106 trypsinized WT A549 cells were washed with PBS twice and resuspended in 600 μl of HEPES-sucrose-Ficoll (HSF) solution (20 mM HEPES-KOH, 6.25% Ficoll, 0.27 M sucrose, 3 mM CaCl2, 2 mM MgCl2) with 50-μg/ml digitonin and EDTA-free protease inhibitor cocktail (Roche). The cells were kept on ice for 10 min, before they were spun down at 1,000 × g for 3 min. The supernatant was collected and then further centrifuged at 15,000 × g for 10 min to generate the cytosol fraction. The nucleus pellet from the first centrifugation was rinsed with HSF buffer once and spun down again at 1,000 × g for 3 min. The supernatant was collected as the washed fraction, and the pellet was then lysed in 50 μl of RIPA buffer with EDTA-free protease inhibitor cocktail (Roche) on ice for 20 min. The lysed nuclei were then centrifuged at 10,000 × g for 10 min, before the supernatant was collected as the nuclear fraction for Western blot analysis. The antibodies used for this experiment included mouse anti-alpha-tubulin antibody (clone DM1A; catalog number 14-4502-82; Thermo Fisher), anti-TATA-binding protein (catalog number 8515s; Cell Signaling Technology), and mouse anti-RTFDC1 antibody (clone 1E8; catalog number LS-C340588; LifeSpan Biosciences).
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