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Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Additionally we are shipping Ribosomal Protein S24 Antibodies (30) and Ribosomal Protein S24 Proteins (14) and many more products for this protein.
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The results show that RPS19 (show RPS19 ELISA Kits), RPS21 (show RPS21 ELISA Kits) or RPS24 are upregulated in malignant tissue and may serve as putative biomarkers for prostate cancer.
findings suggest that two rare heterozygous truncating variations (RPS24 Q191X and CD300LF (show IREM1 ELISA Kits) P261fsX266) are risk candidates for autism spectrum disorder.
RPS24 gene may be a promising biomarker for therapy in human colon cancer and may have a potential application in the diagnosis or treatment of human colon cancer.
Cells from Diamond-Blackfan anemia patients carrying mutations in RPS24 have defective pre-rRNA maturation, as in the case of RPS19 (show RPS19 ELISA Kits) mutations.
Primary fibroblasts from Diamond-Blackfan anemia patients with truncating mutations in RPS19 (show RPS19 ELISA Kits) or in RPS24 have a marked reduction in proliferative capacity.
Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S24E family of ribosomal proteins. It is located in the cytoplasm. Multiple transcript variants encoding different isoforms have been found for this gene. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. Mutations in this gene result in Diamond-Blackfan anemia.
40S ribosomal protein S24
, MRP S24