RPGR1抗体应用：WB 1:500-2000 This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness. [provided by RefSeq, Oct 2008],

RPOM抗体应用：WB 1:500-2000 ELISA 1:5000-20000RNA polymerase mitochondrial(POLRMT) Homo sapiens This gene encodes a mitochondrial DNA-directed RNA polymerase. The gene product is responsible for mitochondrial gene expression as well as for providing RNA primers for initiation of replication of the mitochondrial genome. Although this polypeptide has the same function as the three nuclear DNA-directed RNA polymerases, it is more closely related to RNA polymerases of phage and mitochondrial polymerases of lower eukaryotes. [provided by RefSeq, Jul 2008],

RPR1B抗体应用：WB 1:500-2000

RPRD2抗体应用：WB 1:500-2000 ELISA 1:5000-20000PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Contains 1 CID domain.,

RPRM抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:May be involved in the regulation of p53-dependent G2 arrest of the cell cycle. Seems to induce cell cycle arrest by inhibiting CDC2 activity and nuclear translocation of the CDC2 cyclin B1 complex.,induction:By TP53/p53, following X-ray irradiation.,miscellaneous:'Reprimo' signifies stop/repress.,similarity:Belongs to the reprimo family.,

RPTOR抗体应用：WB 1:500-2000 ELISA 1:5000-20000regulatory associated protein of MTOR complex 1(RPTOR) Homo sapiens This gene encodes a component of a signaling pathway that regulates cell growth in response to nutrient and insulin levels. The encoded protein forms a stoichiometric complex with the mTOR kinase, and also associates with eukaryotic initiation factor 4E-binding protein-1 and ribosomal protein S6 kinase. The protein positively regulates the downstream effector ribosomal protein S6 kinase, and negatively regulates the mTOR kinase. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009],

RRAGD抗体应用：WB 1:500-2000 ELISA 1:5000-20000Ras related GTP binding D(RRAGD) Homo sapiens RRAGD is a monomeric guanine nucleotide-binding protein, or G protein. By binding GTP or GDP, small G proteins act as molecular switches in numerous cell processes and signaling pathways.[supplied by OMIM, Apr 2004],

RRAS抗体应用：WB 1:500-2000 ELISA 1:5000-20000related RAS viral (r-ras) oncogene homolog(RRAS) Homo sapiens The protein encoded by this gene is a small GTPase involved in diverse processes including angiogenesis, vascular homeostasis and regeneration, cell adhesion, and neuronal axon guidance. Mutations in this gene are found in many invasive cancers. [provided by RefSeq, Jul 2015],

RRAS2抗体应用：WB 1:500-2000 ELISA 1:5000-20000related RAS viral (r-ras) oncogene homolog 2(RRAS2) Homo sapiens This gene encodes a member of the R-Ras subfamily of Ras-like small GTPases. The encoded protein associates with the plasma membrane and may function as a signal transducer. This protein may play an important role in activating signal transduction pathways that control cell proliferation. Mutations in this gene are associated with the growth of certain tumors. Pseudogenes of this gene are found on chromosomes 1 and 2. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2010],

RRBP1抗体应用：WB 1:500-2000 ELISA 1:5000-20000ribosome binding protein 1(RRBP1) Homo sapiens This gene encodes a ribosome-binding protein of the endoplasmic reticulum (ER) membrane. Studies suggest that this gene plays a role in ER proliferation, secretory pathways and secretory cell differentiation, and mediation of ER-microtubule interactions. Alternative splicing has been observed and protein isoforms are characterized by regions of N-terminal decapeptide and C-terminal heptad repeats. Splicing of the tandem repeats results in variations in ribosome-binding affinity and secretory function. The full-length nature of variants which differ in repeat length has not been determined. Pseudogenes of this gene have been identified on chromosomes 3 and 7, and RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome, the result of a mutation in a nearby gene on chromosome 20p12. [provided by RefSeq, Apr 2012],