BD-PT4126

Ribosomal Protein S19 Rabbit Polyclonal Antibody

RPS19; 40S ribosomal protein S19

常规抗体

RPS19

40S ribosomal protein S19

WB

Human,Mouse,Rat

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

6223

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6223

P39019

http://www.uniprot.org/uniprotkb/P39019/entry

20085

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20085

Q9CZX8

http://www.uniprot.org/uniprot/Q9CZX8

100910000

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=100910336

P17074

http://www.uniprot.org/uniprot/P17074

The antiserum was produced against synthesized peptide derived from human RPS19. AA range:81-130

Ribosomal Protein S19 Polyclonal Antibody detects endogenous levels of Ribosomal Protein S19 protein.

WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:10000.. IF 1:50-200

16kD

-20°C/1 year

Polyclonal, Rabbit,IgG

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

Higher level expression is seen in the colon carcinoma tissue than normal colon tissue.

Nucleus . Located more specifically in the nucleoli.

Ribosome;

disease:Defects in RPS19 are the cause of Diamond-Blackfan anemia type 1 (DBA1) [MIM:105650]. DBA1 is a form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40% of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies.,function:Required for pre-rRNA processing and maturation of 40S ribosomal subunits.,similarity:Belongs to the ribosomal protein S19e family.,subcellular location:Located more specifically in the nucleoli.,subunit:Interacts with RPS19BP1.,tissue specificity:Higher level expression is seen in the colon carcinoma tissue than normal colon tissue.,

现货

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.