NRK抗体应用：WB 1:500-2000 ELISA 1:5000-20000Nik related kinase(NRK) Homo sapiens The mouse ortholog of this gene encodes a protein kinase required for JNK activation. The encoded protein may be involved in the induction of actin polymerization in late embryogenesis.[provided by RefSeq, Jun 2010],

NRN1抗体应用：WB 1:500-2000 ELISA 1:5000-20000neuritin 1(NRN1) Homo sapiens This gene encodes a member of the neuritin family, and is expressed in postmitotic-differentiating neurons of the developmental nervous system and neuronal structures associated with plasticity in the adult. The expression of this gene can be induced by neural activity and neurotrophins. The encoded protein contains a consensus cleavage signal found in glycosylphoshatidylinositol (GPI)-anchored proteins. The encoded protein promotes neurite outgrowth and arborization, suggesting its role in promoting neuritogenesis. Overexpression of the encoded protein may be associated with astrocytoma progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013],

NRSN2抗体应用：WB 1:500-2000 ELISA 1:5000-20000caution:It is uncertain whether Met-1 or Met-2 is the initiator.,function:May play a role in maintenance and/or transport of vesicles.,similarity:Belongs to the VMP family.,

NRX1B抗体应用：WB 1:500-2000 ELISA 1:5000-20000alternative products:A number of isoforms are produced by alternative promoter usage including the alpha-type (shown here) and beta-type (AC P58400) isoforms which differ in their N-terminus. Additional isoforms may be produced by alternative splicing,alternative products:A number of isoforms, alpha-type (AC Q9ULB1) and beta-type (shown here), are produced by alternative promoter usage. Beta-type isoforms differ from alpha-type isoforms in their N-terminus,function:Neuronal cell surface protein that may be involved in cell recognition and cell adhesion by forming intracellular junctions through binding to neuroligins. May play a role in formation or maintenance of synaptic junctions. May mediate intracellular signaling.,function:Neuronal cell surface protein that may be involved in cell recognition and cell adhesion. May mediate intracellular signaling.,PTM:Highly O-glycosylated and minor N-glycosylated.,PTM:N- and O-glycosylated.,similarity:Be

NRX3A抗体应用：WB 1:500-2000 ELISA 1:5000-20000alternative products:A number of isoforms, alpha-type (AC Q9Y4C0) and beta-type (shown here), are produced by alternative promoter usage. Beta-type isoforms differ from alpha-type isoforms in their N-terminus,alternative products:A number of isoforms, alpha-type (shown here) and beta-type (AC Q9HDB5), are produced by alternative promoter usage. Beta-type isoforms differ from alpha-type isoforms in their N-terminus. Additional isoforms produced by alternative splicing seem to exist,function:Neuronal cell surface protein that may be involved in cell recognition and cell adhesion.,function:Neuronal cell surface protein that may be involved in cell recognition and cell adhesion. May mediate intracellular signaling.,similarity:Belongs to the neurexin family.,similarity:Contains 1 laminin G-like domain.,similarity:Contains 3 EGF-like domains.,similarity:Contains 6 laminin G-like domains.,subunit:The cytoplasmic C-terminal region binds to CASK (By sim

NSA2抗体应用：WB 1:500-2000 ELISA 1:5000-20000NSA2, ribosome biogenesis homolog(NSA2) Homo sapiens This gene encodes a nucleolar protein involved in cell cycle regulation and proliferation. This gene was identified based on sequence similarity to a highly conserved Saccharomyces cerevisiae gene encoding a pre-ribosomal protein, which is involved in large ribosomal subunit biogenesis. The encoded protein is found at elevated levels in diabetic nephropathy. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified. [provided by RefSeq, Nov 2012],

NSD3抗体应用：WB 1:500-2000 This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. This protein methylates histone H3 at lysine residues 4 and 27, which represses gene transcription. Two alternatively spliced variants have been described. [provided by RefSeq, May 2015],

NSE2抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:E3 SUMO-protein ligase component of the SMC5-SMC6 complex, a complex involved in DNA double-strand breaks by homologous recombination. The complex may promote sister chromatid homologous recombination by recruiting the SMC1-SMC3 cohesin complex to double-strand breaks. Acts as a E3 ligase mediating SUMO attachment to various proteins such as SMC6L1 and TRAX, and maybe the cohesin components RAD21 and STAG2. SUMO protein-ligase activity is required for the prevention of DNA damage-induced apoptosis by facilitating DNA repair.,pathway:Protein modification; protein sumoylation.,PTM:Sumoylated, possibly via autosumoylation.,similarity:Belongs to the NSE2 family.,similarity:Contains 1 SP-RING-type zinc finger.,subunit:Component of the SMC5-SMC6 complex which consists of SMC5, SMC6, NSMCE2/MMS21 and probably NSMCE1.,

NSUN2抗体应用：WB 1:500-2000 This gene encodes a methyltransferase that catalyzes the methylation of cytosine to 5-methylcytosine (m5C) at position 34 of intron-containing tRNA(Leu)(CAA) precursors. This modification is necessary to stabilize the anticodon-codon pairing and correctly translate the mRNA. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Mar 2011],

NSUN5抗体应用：WB 1:500-2000 ELISA 1:5000-20000NOP2/Sun RNA methyltransferase family member 5(NSUN5) Homo sapiens This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013],