REL1抗体应用：WB 1:500-2000 ELISA 1:5000-20000relaxin 1(RLN1) Homo sapiens Relaxins are known endocrine and autocrine/paracrine hormones, belonging to the insulin gene superfamily. In humans there are three non-allelic relaxin genes, RLN1, RLN2 and RLN3, where RLN1 and RLN2 share high sequence homology. The protein encoded by this gene is synthesized as a single-chain polypeptide but the active form consists of an A chain and a B chain linked by disulfide bonds. Relaxin is produced by the ovary, and targets the mammalian reproductive system to ripen the cervix, elongate the pubic symphysis and inhibit uterine contraction. It may have additional roles in enhancing sperm motility, regulating blood pressure, controlling heart rate and releasing oxytocin and vasopressin. [provided by RefSeq, Jan 2013],

REL2抗体应用：WB 1:500-2000 ELISA 1:5000-20000relaxin 2(RLN2) Homo sapiens This gene encodes a member of the relaxin subfamily and insulin superfamily of peptide hormones. In humans there are three non-allelic relaxin genes. This gene encodes multiple protein isoforms, at least one of which undergoes proteolytic processing. This processing generates relaxin A and B chains that are linked by disulfide bonds to form the mature peptide hormone. This hormone plays a role in the male and female reproductive systems and was initially noted for its role in pregnancy. This protein also plays broader roles in the cardiovascular system, including in the regulation of blood pressure and control of heart rate, and data from animal models shows that this protein may have anti-fibrotic and cardioprotective effects. [provided by RefSeq, Jul 2016],

RELN抗体应用：IHC-p 1:50-300reelin(RELN) Homo sapiens This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008],

REM1抗体应用：WB 1:500-2000 ELISA 1:5000-20000RRAD and GEM like GTPase 1(REM1) Homo sapiens The protein encoded by this gene is a GTPase and member of the RAS-like GTP-binding protein family. The encoded protein is expressed in endothelial cells, where it promotes reorganization of the actin cytoskeleton and morphological changes in the cells. [provided by RefSeq, Jul 2008],

REM2抗体应用：WB 1:500-2000 ELISA 1:5000-20000caution:It is uncertain whether Met-1 or Met-59 is the initiator.,function:Binds GTP saturably and exhibits a low intrinsic rate of GTP hydrolysis.,similarity:Belongs to the small GTPase superfamily. RGK family.,

REPI1抗体应用：WB 1:500-2000

REPS2抗体应用：WB 1:500-2000 ELISA 1:5000-20000RALBP1 associated Eps domain containing 2(REPS2) Homo sapiens The product of this gene is part of a protein complex that regulates the endocytosis of growth factor receptors. The encoded protein directly interacts with a GTPase activating protein that functions downstream of the small G protein Ral. Its expression can negatively affect receptor internalization and inhibit growth factor signaling. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

PYGO2抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Involved in signal transduction through the Wnt pathway.,sequence caution:Sequencing errors.,similarity:Contains 1 PHD-type zinc finger.,subunit:Binds to BCL9 via the PHD-type zinc finger motif, and thereby becomes part of the nuclear beta-catenin/TCF complex.,

PZP抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Is able to inhibit all four classes of proteinases by a unique 'trapping' mechanism. This protein has a peptide stretch, called the 'bait region' which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change is induced in the protein which traps the proteinase. The entrapped enzyme remains active against low molecular weight substrates (activity against high molecular weight substrates is greatly reduced). Following cleavage in the bait region a thioester bond is hydrolyzed and mediates the covalent binding of the protein to the proteinase.,similarity:Belongs to the protease inhibitor I39 (alpha-2-macroglobulin) family.,subunit:Homotetramer, which consists of two pairs of disulfide-linked chains.,tissue specificity:Plasma. Prominent constituent of late-pregnancy sera.,

QSER1抗体应用：WB 1:500-2000 ELISA 1:5000-20000PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,