SUGP1抗体应用：WB 1:500-2000 ELISA 1:5000-20000SURP and G-patch domain containing 1(SUGP1) Homo sapiens SF4 is a member of the SURP family of splicing factors.[supplied by OMIM, Sep 2003],

SUH抗体应用：WB 1:500-2000 ELISA 1:5000-20000recombination signal binding protein for immunoglobulin kappa J region(RBPJ) Homo sapiens The protein encoded by this gene is a transcriptional regulator important in the Notch signaling pathway. The encoded protein acts as a repressor when not bound to Notch proteins and an activator when bound to Notch proteins. It is thought to function by recruiting chromatin remodeling complexes containing histone deacetylase or histone acetylase proteins to Notch signaling pathway genes. Several transcript variants encoding different isoforms have been found for this gene, and several pseudogenes of this gene exist on chromosome 9. [provided by RefSeq, Oct 2013],

SUMO2抗体应用：WB 1:500-2000 ELISA 1:5000-20000small ubiquitin-like modifier 2(SUMO2) Homo sapiens This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitin which targets proteins for degradation, this protein is involved in a variety of cellular processes, such as nuclear transport, transcriptional regulation, apoptosis, and protein stability. It is not active until the last two amino acids of the carboxy-terminus have been cleaved off. Numerous pseudogenes have been reported for this gene. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008],

SUMO3抗体应用：WB 1:500-2000 ELISA 1:5000-20000small ubiquitin-like modifier 3(SUMO3) Homo sapiens This gene encodes a member of the small ubiquitin-related modifier (SUMO) family of eukaryotic proteins. The encoded protein is covalently conjugated to other proteins via a post-translation modification known as sumoylation. Sumoylation may play a role in a wide variety of cellular processes, including nuclear transport, DNA replication and repair, mitosis, transcriptional regulation, and signal transduction. Alternatively spliced transcript variants encoding distinct proteins have been described. [provided by RefSeq, Feb 2014],

SUMO4抗体应用：WB 1:500-2000 ELISA 1:5000-20000small ubiquitin-like modifier 4(SUMO4) Homo sapiens This gene is a member of the SUMO gene family. This family of genes encode small ubiquitin-related modifiers that are attached to proteins and control the target proteins' subcellular localization, stability, or activity. The protein described in this record is located in the cytoplasm and specifically modifies IKBA, leading to negative regulation of NF-kappa-B-dependent transcription of the IL12B gene. A specific polymorphism in this SUMO gene, which leads to the M55V substitution, has been associated with type I diabetes. The RefSeq contains this polymorphism. [provided by RefSeq, Jul 2008],

SUN5抗体应用：WB 1:500-2000 ELISA 1:5000-20000similarity:Contains 1 Unc84 (SUN) domain.,tissue specificity:Widely expressed.,

SUOX抗体应用：WB 1:500-2000Sulfite oxidase is a homodimeric protein localized to the intermembrane space of mitochondria. Each subunit contains a heme domain and a molybdopterin-binding domain. The enzyme catalyzes the oxidation of sulfite to sulfate, the final reaction in the oxidative degradation of the sulfur amino acids cysteine and methionine. Sulfite oxidase deficiency results in neurological abnormalities which are often fatal at an early age. Alternative splicing results in multiple transcript variants encoding identical proteins. [provided by RefSeq, Jul 2008],

SUV91抗体应用：WB 1:500-2000 ELISA 1:5000-20000suppressor of variegation 3-9 homolog 1(SUV39H1) Homo sapiens This gene encodes an evolutionarily-conserved protein containing an N-terminal chromodomain and a C-terminal SET domain. The encoded protein is a histone methyltransferase that trimethylates lysine 9 of histone H3, which results in transcriptional gene silencing. Loss of function of this gene disrupts heterochromatin formation and may cause chromosome instability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013],

SV2A抗体应用：WB 1:500-2000 ELISA 1:5000-20000synaptic vesicle glycoprotein 2A(SV2A) Homo sapiens The protein encoded by this gene is one of three related synaptic vesicle proteins. The encoded protein may interact with synaptotagmin to enhance low frequency neurotransmission in quiescent neurons. [provided by RefSeq, Jun 2016],

SV2B抗体应用：WB 1:500-2000 ELISA 1:5000-20000synaptic vesicle glycoprotein 2B(SV2B) Homo sapiens This gene encodes a member of the synaptic vesicle proteins 2 (SV2) family and major facilitator superfamily of proteins. This protein and other members of the family are localized to synaptic vesicles and may function in the regulation of vesicle trafficking and exocytosis. Studies in mice suggest that the encoded protein may act as a protein receptor for botulinum neurotoxin E in neurons, and that this protein may be important for the integrity of the glomerular filtration barrier. This gene shows reduced expression in areas of synaptic loss in the hippocampus of human temporal lobe epilepsy patients. [provided by RefSeq, Sep 2016],