TPC2L抗体应用：WB 1:500-2000 ELISA 1:5000-20000trafficking protein particle complex 2 like(TRAPPC2L) Homo sapiens This gene encodes a protein that interacts with the tethering factor trafficking protein particle (TRAPP complex). TRAPP complexes mediate the contact between vescicles and target membranes, and thus, are involved in vescicle-mediated transport of proteins and lipids. The encoded protein is related to the X-linked trafficking protein particle complex 2. A related pseudogene is located on the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016],

TPC6B抗体应用：WB 1:500-2000 ELISA 1:5000-20000trafficking protein particle complex 6B(TRAPPC6B) Homo sapiens TRAPPC6B is a component of TRAPP complexes, which are tethering complexes involved in vesicle transport (Kummel et al., 2005 [PubMed 16025134]).[supplied by OMIM, Mar 2008],

TPD53抗体应用：WB 1:500-2000 ELISA 1:5000-20000tumor protein D52-like 1(TPD52L1) Homo sapiens This gene encodes a member of a family of proteins that contain coiled-coil domains and may form hetero- or homomers. The encoded protein is involved in cell proliferation and calcium signaling. It also interacts with the mitogen-activated protein kinase kinase kinase 5 (MAP3K5/ASK1) and positively regulates MAP3K5-induced apoptosis. Multiple alternatively spliced transcript variants have been observed. [provided by RefSeq, Jan 2016],

STAC3抗体应用：WB 1:500-2000 ELISA 1:5000-20000SH3 and cysteine rich domain 3(STAC3) Homo sapiens The protein encoded by this gene is a component of the excitation-contraction coupling machinery of muscles. This protein is a member of the Stac gene family and contains an N-terminal cysteine-rich domain and two SH3 domains. Mutations in this gene are a cause of Native American myopathy. [provided by RefSeq, Nov 2013],

SH3L3抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Could act as a modulator of glutaredoxin biological activity.,similarity:Belongs to the SH3BGR family.,similarity:Contains 1 glutaredoxin domain.,tissue specificity:Ubiquitous.,

SHAN3抗体应用：WB 1:500-2000 ELISA 1:5000-20000SH3 and multiple ankyrin repeat domains 3(SHANK3) Homo sapiens This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar

SHBG抗体应用：WB 1:500-2000 ELISA 1:5000-20000sex hormone binding globulin(SHBG) Homo sapiens This gene encodes a steroid binding protein that was first described as a plasma protein secreted by the liver but is now thought to participate in the regulation of steroid responses. The encoded protein transports androgens and estrogens in the blood, binding each steroid molecule as a dimer formed from identical or nearly identical monomers. Polymorphisms in this gene have been associated with polycystic ovary syndrome and type 2 diabetes mellitus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014],

SHE抗体应用：WB 1:500-2000 ELISA 1:5000-20000similarity:Contains 1 SH2 domain.,

SHOX抗体应用：WB 1:500-2000 ELISA 1:5000-20000short stature homeobox(SHOX) Homo sapiens This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jul 2008],

SHPS1抗体应用：WB 1:500-2000 ELISA 1:5000-20000signal regulatory protein alpha(SIRPA) Homo sapiens The protein encoded by this gene is a member of the signal-regulatory-protein (SIRP) family, and also belongs to the immunoglobulin superfamily. SIRP family members are receptor-type transmembrane glycoproteins known to be involved in the negative regulation of receptor tyrosine kinase-coupled signaling processes. This protein can be phosphorylated by tyrosine kinases. The phospho-tyrosine residues of this PTP have been shown to recruit SH2 domain containing tyrosine phosphatases (PTP), and serve as substrates of PTPs. This protein was found to participate in signal transduction mediated by various growth factor receptors. CD47 has been demonstrated to be a ligand for this receptor protein. This gene and its product share very high similarity with several other members of the SIRP family. These related genes are located in close proximity to each other on chromosome 20p13. Multiple alternati