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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 Proteins (15) and Ribosomal Protein S24 Kits (12) and many more products for this protein.
Showing 10 out of 29 products:
Human Polyclonal RPS24 Primary Antibody for EIA, WB - ABIN954616
Badhai, Fröjmark, J Davey, Schuster, Dahl: Ribosomal protein S19 and S24 insufficiency cause distinct cell cycle defects in Diamond-Blackfan anemia. in Biochimica et biophysica acta 2009
Show all 3 references for ABIN954616
Human Polyclonal RPS24 Primary Antibody for ICC, IF - ABIN4351177
Badhai, Fröjmark, Razzaghian, Davey, Schuster, Dahl: Posttranscriptional down-regulation of small ribosomal subunit proteins correlates with reduction of 18S rRNA in RPS19 deficiency. in FEBS letters 2009
Show all 2 references for ABIN4351177
Human Polyclonal RPS24 Primary Antibody for WB - ABIN4891476
Wang, Sui, Li, Cao, He, Yang, Zhu, Sun, Pu: RPS24 knockdown inhibits colorectal cancer cell migration and proliferation in vitro. in Gene 2015
Human Polyclonal RPS24 Primary Antibody for FACS, WB - ABIN653681
Robledo, Idol, Crimmins, Ladenson, Mason, Bessler: The role of human ribosomal proteins in the maturation of rRNA and ribosome production. in RNA (New York, N.Y.) 2008
Cow (Bovine) Polyclonal RPS24 Primary Antibody for WB - ABIN2778735
Choesmel, Fribourg, Aguissa-Touré, Pinaud, Legrand, Gazda, Gleizes: Mutation of ribosomal protein RPS24 in Diamond-Blackfan anemia results in a ribosome biogenesis disorder. in Human molecular genetics 2008
findings suggest that two rare heterozygous truncating variations (RPS24 Q191X and CD300LF (show IREM1 Antibodies) 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 Antibodies) mutations.
Primary fibroblasts from Diamond-Blackfan anemia patients with truncating mutations in RPS19 (show RPS19 Antibodies) 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