GRHPR抗体应用：WB 1:500-2000 This gene encodes an enzyme with hydroxypyruvate reductase, glyoxylate reductase, and D-glycerate dehydrogenase enzymatic activities. The enzyme has widespread tissue expression and has a role in metabolism. Type II hyperoxaluria is caused by mutations in this gene. [provided by RefSeq, Jul 2008],

GRIF-1抗体应用：Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. PTM:O-glycosylated.,similarity:Contains 1 HAP1 N-terminal domain.,subunit:Interacts with GABA-A receptor and O-GlcNAc transferase (By similarity). Interacts with RHOT1/Miro-1 and RHOT2/Miro-2.,tissue specificity:Widely expressed, with highest expression in heart.,

GRIK3抗体应用：WB 1:500-2000 Glutamate receptors are the predominant excitatory neurotransmitter receptors in the mammalian brain and are activated in a variety of normal neurophysiologic processes. This gene product belongs to the kainate family of glutamate receptors, which are composed of four subunits and function as ligand-activated ion channels. It is not certain if the subunit encoded by this gene is subject to RNA editing as the other 2 family members (GRIK1 and GRIK2). A Ser310Ala polymorphism has been associated with schizophrenia, and there are conflicting reports of its association with the pathogenesis of delirium tremens in alcoholics. [provided by RefSeq, Jul 2008],

GRIN1抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/40000. function:May be involved in neurite outgrowth.,PTM:Palmitoylation on Cys-999 and/or Cys-1000 is required for membrane targeting.,subcellular location:Highly enriched in growth cone.,subunit:Interacts with activated forms of GNAI1, GNAO1 and GNAZ.,tissue specificity:Widely expressed in the central nervous system, with highest levels in spinal cord.,

GRIN1抗体应用：WB 1:500-2000, ELISA 1:10000-20000 glutamate ionotropic receptor NMDA type subunit 1(GRIN1) Homo sapiens The protein encoded by this gene is a critical subunit of N-methyl-D-aspartate receptors, members of the glutamate receptor channel superfamily which are heteromeric protein complexes with multiple subunits arranged to form a ligand-gated ion channel. These subunits play a key role in the plasticity of synapses, which is believed to underlie memory and learning. Cell-specific factors are thought to control expression of different isoforms, possibly contributing to the functional diversity of the subunits. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2008],

GRIN2抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. function:May be involved in neurite outgrowth.,subunit:Interacts with activated forms of GNAO1 and GNAZ.,tissue specificity:Expressed specifically in the cerebellum.,

GRIN2D抗体应用：WB 1:500-2000, ELISA 1:10000-20000 glutamate ionotropic receptor NMDA type subunit 2D(GRIN2D) Homo sapiens N-methyl-D-aspartate (NMDA) receptors are a class of ionotropic glutamate receptors. NMDA channel has been shown to be involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. NMDA receptor channels are heteromers composed of the key receptor subunit NMDAR1 (GRIN1) and 1 or more of the 4 NMDAR2 subunits: NMDAR2A (GRIN2A), NMDAR2B (GRIN2B), NMDAR2C (GRIN2C), and NMDAR2D (GRIN2D). [provided by RefSeq, Mar 2010],

GRIN3抗体应用：Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. function:May be involved in neurite outgrowth.,

GRIP-1抗体应用：Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. nuclear receptor coactivator 2(NCOA2) Homo sapiens The protein encoded by this gene functions as a transcriptional coactivator for nuclear hormone receptors, including steroid, thyroid, retinoid, and vitamin D receptors. The encoded protein acts as an intermediary factor for the ligand-dependent activity of these nuclear receptors, which regulate their target genes upon binding of cognate response elements. This gene has been found to be involved in translocations that result in fusions with other genes in various cancers, including the lysine acetyltransferase 6A (KAT6A) gene in acute myeloid leukemia, the ETS variant 6 (ETV6) gene in acute lymphoblastic leukemia, and the hes related family bHLH transcription factor with YRPW motif 1 (HEY1) gene in mesenchymal chondrosarcoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016],

GRK 1抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. G protein-coupled receptor kinase 1(GRK1) Homo sapiens This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates rhodopsin and initiates its deactivation. Defects in GRK1 are known to cause Oguchi disease 2 (also known as stationary night blindness Oguchi type-2). [provided by RefSeq, Jul 2008],