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Mrps16

Manufactured by Proteintech

MRPS16 is a protein that is a component of the mitochondrial ribosome. Mitochondrial ribosomes are responsible for synthesizing proteins necessary for the function of mitochondria, the organelles that generate energy in eukaryotic cells.

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2 protocols using mrps16

1

Immunoblot Analysis of Mitochondrial Proteins

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Specific proteins were detected using rabbit polyclonal antibodies against: MRPL44 (16394-1-AP), MRPL23 (11706-1-AP), TACO1 (21147-1-AP), MRPS35 (16457-1-AP), MRPS16 (16735-1-AP) (Proteintech, diluted 1:1,000), MRPS34 (Sigma HPA042112, diluted 1:1,000), and mouse monoclonal antibodies against: β-actin (8226), porin (14734), NDUFA9 (14713), complex II (14715), complex III (14745), COXI (14705), COXII (198286), COXIV (14744) and complex V subunit a (14748; Abcam, diluted 1:1,000), in Odyssey Blocking Buffer (Li-Cor). IR Dye 800CW Goat Anti-Rabbit IgG or IRDye 680LT Goat Anti-Mouse IgG (Li-Cor) secondary antibodies were used and the immunoblots were visualized using an Odyssey Infrared Imaging System (Li-Cor). Examples of uncropped blots are shown in the Supplementary Fig. 8. Tissue-specific analysis was performed using a Proteintech mouse tissue blot (Cat. No M10005).
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2

Comprehensive Protein Detection Workflow

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Specific proteins were detected using rabbit polyclonal antibodies against: MRPL44, MRPL37, MRPL23, MRPS12, MRPS16 (Proteintech, diluted 1:1000), MRPS34 (Sigma, diluted 1:1000), GAPDH, phosphorylated and non‐phosphorylated S6, phosphorylated and non‐phosphorylated Akt, phosphorylated and non‐phosphorylated 4EBP (Cell Signalling Technology, diluted 1:500) and mouse monoclonal antibodies against: phosphorylated and non‐phosphorylated AMPKα (Cell Signalling Technology, diluted 1:500), COXII (Abcam, diluted 1:1000), phosphorylated and non‐phosphorylated YAP, AFG3L2, LC3A/B, Glut2, Glut4, and Total OXPHOS Rodent WB Antibody Cocktail (Abcam, Diluted 1:1000) in Odyssey Blocking Buffer (Li‐Cor). IR Dye 800CW Goat Anti‐Rabbit IgG or IRDye 680LT Goat Anti‐Mouse IgG (Li‐Cor) secondary antibodies were used and the immunoblots were visualized using an Odyssey Infrared Imaging System (Li‐Cor).
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