PNISR抗体应用：WB 1:500-2000 ELISA 1:5000-20000PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,sequence caution:Contaminating sequence. Potential poly-A sequence.,similarity:Belongs to the splicing factor SR family.,subunit:Interacts with PNN.,tissue specificity:Expressed in heart, skeletal muscle, thymus, spleen, kidney, liver, placenta and leukocytes.,

PNKD抗体应用：WB 1:500-2000 ELISA 1:5000-20000paroxysmal nonkinesigenic dyskinesia(PNKD) Homo sapiens This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010],

PNKP抗体应用：WB 1:500-2000 ELISA 1:5000-20000polynucleotide kinase 3'-phosphatase(PNKP) Homo sapiens This locus represents a gene involved in DNA repair. In response to ionizing radiation or oxidative damage, the protein encoded by this locus catalyzes 5' phosphorylation and 3' dephosphorylation of nucleic acids. Mutations at this locus have been associated with microcephaly, seizures, and developmental delay.[provided by RefSeq, Sep 2010],

PNMA1抗体应用：WB 1:500-2000This gene encodes a neuron- and testis-specific protein that is also expressed in some paraneoplastic syndromes affecting the nervous system. Some patients with neurologic disorders develop antibodies against the protein encoded by this gene. The identification of the antineuronal antibodies in the sera of these patients has facilitated the diagnosis of paraneoplastic neurological disorders and the early detection of the associated tumors. [provided by RefSeq, Feb 2014],

PNMT抗体应用：WB 1:500-2000 ELISA 1:5000-20000The product of this gene catalyzes the last step of the catecholamine biosynthesis pathway, which methylates norepinephrine to form epinephrine (adrenaline). The enzyme also has beta-carboline 2N-methyltransferase activity. This gene is thought to play a key step in regulating epinephrine production. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2012],

PO3F2抗体应用：WB 1:500-2000 ELISA 1:5000-20000POU class 3 homeobox 2(POU3F2) Homo sapiens This gene encodes a member of the POU-III class of neural transcription factors. The encoded protein is involved in neuronal differentiation and enhances the activation of corticotropin-releasing hormone regulated genes. Overexpression of this protein is associated with an increase in the proliferation of melanoma cells. [provided by RefSeq, Mar 2012],

PO3F3抗体应用：WB 1:500-2000 ELISA 1:5000-20000POU class 3 homeobox 3(POU3F3) Homo sapiens This gene encodes a POU-domain containing protein that functions as a transcription factor. The encoded protein recognizes an octamer sequence in the DNA of target genes. This protein may play a role in development of the nervous system. [provided by RefSeq, Apr 2015],

PO5F2抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Transcription factor that binds preferentially to the octamer motif (5'-ATGTTAAT-3'). May exert a regulatory function in meiotic events that are required for terminal differentiation of male germ cell.,similarity:Belongs to the POU transcription factor family. Class-5 subfamily.,similarity:Contains 1 homeobox DNA-binding domain.,similarity:Contains 1 POU-specific domain.,tissue specificity:Expressed in skeletal and cardiac muscles, brain, heart and lung. Little or no detectable expression found in pancreas, kidney, liver or placenta.,

PODO抗体应用：WB 1:500-2000 ELISA 1:5000-20000NPHS2, podocin(NPHS2) Homo sapiens This gene encodes a protein that plays a role in the regulation of glomerular permeability. Mutations in this gene cause steroid-resistant nephrotic syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014],

POGZ抗体应用：WB 1:500-2000 ELISA 1:5000-20000pogo transposable element with ZNF domain(POGZ) Homo sapiens The protein encoded by this gene appears to be a zinc finger protein containing a transposase domain at the C-terminus. This protein was found to interact with the transcription factor SP1 in a yeast two-hybrid system. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Aug 2010],