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anti-Human RPS19 Antibodies:
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Human Monoclonal RPS19 Primary Antibody for ELISA, WB - ABIN562734
Rey, Duffy, Brown, Kennedy, Dick, Dror, Tailor: Enhanced alternative splicing of the FLVCR1 gene in Diamond Blackfan anemia disrupts FLVCR1 expression and function that are critical for erythropoiesis. in Haematologica 2008
Show all 5 Pubmed References
Human Polyclonal RPS19 Primary Antibody for ELISA, WB - ABIN250880
Léger-Silvestre, Caffrey, Dawaliby, Alvarez-Arias, Gas, Bertolone, Gleizes, Ellis: Specific Role for Yeast Homologs of the Diamond Blackfan Anemia-associated Rps19 Protein in Ribosome Synthesis. in The Journal of biological chemistry 2005
The results show that RPS19, RPS21 (show RPS21 Antibodies) or RPS24 (show RPS24 Antibodies) are upregulated in malignant tissue and may serve as putative biomarkers for prostate cancer.
Study of genetic risk of prevalent hrHPV infections in Nigerian women found significant associations with SNPs on ribosomal protein gene S19 (RPS19) and Thymidylate Synthase (show TYMS Antibodies) gene (TYMS (show TYMS Antibodies)), in an allelic model. This risk remained significant, after adjusting for age, body mass index, smoking, age at menarche, age at sexual debut, lifetime total number of sexual partners and the total number of pregnancies.
Reducing RPS19 in tumor cells or blocking the C5a receptor 1-RPS19 interaction decreases RPS19-mediated immunosuppression, impairs tumor growth, and delays the development of tumors in a transgenic model of breast cancer
RPS19-downregulated erythroleukemia cells show reduced FLVCR1a and FLVCR1b mRNA levels associated with heme overload.
Loss of RPS19 expression is associated with Diamond-Blackfan anemia.
Mutations R62W and R101H impair RPS19 ability to associate with the ribosome.
Data indicate that GATA1 (show GATA1 Antibodies) transcription factor is downregulated in ribosomal protein S19 (RPS19)-deficient cells through upregulation of TNF-alpha (show TNF Antibodies) and p38 MAPK (show MAPK14 Antibodies).
RPS19 mutation is associated with Diamond Blackfan Anemia.
A binding domain for RPS19 was identified and characterized in the N-terminus.
increase of autophagy in cells derived from DBA patients, in CD34 (show CD34 Antibodies)+ erythrocyte progenitor cells with RPS19 knock down, in the red blood cells of zebrafish embryos with RP-deficiency, and in cells from patients with Shwachman-Diamond syndrome
Mutation of the key residue for extraribosomal function of ribosomal protein S19 cause increased grooming behaviors in mice. Results suggest an involvement of RP S19 (show ASAP1 Antibodies) oligomers in some anxiety-like behavior, especially grooming behavior.
Rps19 mutant shows behavioural phenotypes resembling that of the human Diamond-Blackfan anaemia syndrome.
indicate the importance of the RP S19 (show ASAP1 Antibodies) oligomer-induced macrophage recruitment in coagulum resorption
Rps19 mutant embryonic stem cells showed significant increase in p53 (show TP53 Antibodies) protein expression.
We report the generation of mouse models for RPS19-deficient Diamond Blackfan anemia using transgenic RNA interference that allows an inducible and graded down-regulation of Rps19.
generated a transgenic model expressing an RPS19 mutation in which an arginine residue is replaced with a tryptophan residue at codon 62 as a model of Diamond-Blackfan anemia
Combined Rps19 insufficiency and Pim-1 (show PIM1 Antibodies) deficiency promote murine myeloid cell growth through a deregulation of c-Myc (show MYC Antibodies) and a simultaneous up-regulation of anti-apoptotic Bcl proteins.
RPS19 mRNA and protein expression were shown to decrease during terminal erythroid differentiation.
Results indicate that ribosomal protein S19 (-/-) zygotes do not form blastocysts, whereas one normal Rps19 allele in mice is sufficient to maintain normal ribosomal and possibly extraribosomal functions.
presence of an RP S19 (show ASAP1 Antibodies) dimer- and C5a receptor-mediated autocrine-type augmentation mechanism during Mn II-induced apoptosis in the mouse fibroblastic cell line
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 S19E family of ribosomal proteins. It is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia (DBA), a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors, in a subset of patients. This suggests a possible extra-ribosomal function for this gene in erythropoietic differentiation and proliferation, in addition to its ribosomal function. Higher expression levels of this gene in some primary colon carcinomas compared to matched normal colon tissues has been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.
ribosomal protein S19
, 40S ribosomal protein S19