Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Additionally we are shipping RPL5 Proteins (25) and RPL5 Kits (9) and many more products for this protein.
Showing 10 out of 77 products:
Human Polyclonal RPL5 Primary Antibody for EIA, IHC (p) - ABIN954600
Quarello, Garelli, Carando, Brusco, Calabrese, Dufour, Longoni, Misuraca, Vinti, Aspesi, Biondini, Loreni, Dianzani, Ramenghi: Diamond-Blackfan anemia: genotype-phenotype correlations in Italian patients with RPL5 and RPL11 mutations. in Haematologica 2010
Show all 2 references for ABIN954600
Arabidopsis Polyclonal RPL5 Primary Antibody for WB - ABIN2786525
Sun, Dai, Lu: 5-fluorouracil activation of p53 involves an MDM2-ribosomal protein interaction. in The Journal of biological chemistry 2007
Human Polyclonal RPL5 Primary Antibody for ELISA, WB - ABIN1534576
Gregory, Barlow, McLay, Kaul, Swarbreck, Dunham, Scott, Howe, Woodfine, Spencer, Jones, Gillson, Searle, Zhou, Kokocinski, McDonald, Evans, Phillips, Atkinson, Cooper, Jones, Hall, Andrews, Lloyd et al.: The DNA sequence and biological annotation of human chromosome 1. ... in Nature 2006
Ribosomal proteins L11 (show RPL11 Antibodies) and L5 activate TAp73 (show TP73 Antibodies) by overcoming MDM2 (show MDM2 Antibodies) inhibition.
RPL5 mutation is associated with Diamond Blackfan Anemia.
Findings uncover a mechanism by which RPL5 and RPL11 (show RPL11 Antibodies) can co-operatively suppress c-Myc (show MYC Antibodies) expression, allowing a tightly controlled ribosome biogenesis in cells.
Unlike other tumor suppressors, RPL5 and RPL11 play essential roles in normal cell proliferation.
High frequency of RPL5 gene deletion is associated with Italian Diamond-Blackfan anemia.
Oncogenic splicing factor (show SLU7 Antibodies) SRSF1 (show SRSF1 Antibodies) stabilizes the tumor suppressor protein p53 (show TP53 Antibodies) via RPL5, inducing cell senescence.
Mutations affect the ribosomal proteins RPL5 and RPL10 (show RPL10 Antibodies) in 12 of 122 (9.8%) pediatric T-cell acute lymphoblastic leukemias.
disrupted nucleoli may provide a platform for L5- and L11 (show RPL11 Antibodies)-dependent p53 (show TP53 Antibodies) activation, implying a role for the nucleolus in p53 (show TP53 Antibodies) activation by ribosomal biogenesis stress
Data show 1 proband with an RPL5 deletion, 1 patient with an RPL35A (show RPL35A Antibodies) deletion, 3 with RPS17 (show RPS17 Antibodies) deletions, and 1 with an RPS19 (show RPS19 Antibodies) deletion.
Data show that all patients with RPS19 (show RPS19 Antibodies) and RPL5 mutations had physical abnormalities.
there is a fine tuned balance in the interaction of ribosomal proteins with the MDM2 (show MDM2 Antibodies)/p53 (show TP53 Antibodies) axis which is important in normal hematopoiesis.
There was a significant delay in the G2/M phase in Rpl5 mutant cells, unaffected by p53 (show TP53 Antibodies) knockdown.
RpL5, located in the centric heterochromatin of chromosome 2, was analyzed genetically.
eclipse might be a novel ribosome associated protein interacting with dRPL5
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 60S subunit. The protein belongs to the L18P family of ribosomal proteins. It is located in the cytoplasm. The protein binds 5S rRNA to form a stable complex called the 5S ribonucleoprotein particle (RNP), which is necessary for the transport of nonribosome-associated cytoplasmic 5S rRNA to the nucleolus for assembly into ribosomes. The protein interacts specifically with the beta subunit of casein kinase II. Variable expression of this gene in colorectal cancers compared to adjacent normal tissues has been observed, although no correlation between the level of expression and the severity of the disease has been found. This gene is co-transcribed with the small nucleolar RNA gene U21, which is located in its fifth intron. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.
60S ribosomal protein L5
, 60S ribosomal protein L5-like protein
, ribosomal protein L5
, enhancer on chromosome 2, complementation group d
, yippee interacting protein 6
, 60S ribosomal protein L5-B