SPEG抗体应用：IHC-p 1:50-300SPEG complex locus(SPEG) Homo sapiens This gene encodes a protein with similarity to members of the myosin light chain kinase family. This protein family is required for myocyte cytoskeletal development. Along with the desmin gene, expression of this gene may be controlled by the desmin locus control region. Mutations in this gene are associated with centronuclear myopathy 5. [provided by RefSeq, Jun 2016],

SPF45抗体应用：WB 1:500-2000 ELISA 1:5000-20000RNA binding motif protein 17(RBM17) Homo sapiens This gene encodes an RNA binding protein. The encoded protein is part of the spliceosome complex and functions in the second catalytic step of mRNA splicing. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 9 and 15. [provided by RefSeq, Mar 2009],

SPG7抗体应用：WB 1:500-2000 ELISA 1:5000-20000SPG7, paraplegin matrix AAA peptidase subunit(SPG7) Homo sapiens This gene encodes a mitochondrial metalloprotease protein that is a member of the AAA family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Mar 2014],

SPHAR抗体应用：IHC-p 1：50-200

SPHK1抗体应用：WB 1:500-2000 ELISA 1:5000-20000sphingosine kinase 1(SPHK1) Homo sapiens The protein encoded by this gene catalyzes the phosphorylation of sphingosine to form sphingosine-1-phosphate (S1P), a lipid mediator with both intra- and extracellular functions. Intracellularly, S1P regulates proliferation and survival, and extracellularly, it is a ligand for cell surface G protein-coupled receptors. This protein, and its product S1P, play a key role in TNF-alpha signaling and the NF-kappa-B activation pathway important in inflammatory, antiapoptotic, and immune processes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011],

SPI2抗体应用：WB 1:500-2000 ELISA 1:5000-20000serpin family I member 2(SERPINI2) Homo sapiens The gene encodes a member of a family of proteins that acts as inhibitors of serine proteases. These proteins function in the regulation of a variety of physiological processes, including coagulation, fibrinolysis, development, malignancy, and inflammation. Expression of the encoded protein may be downregulated during pancreatic carcinogenesis. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Jan 2013],

SPIT1抗体应用：WB 1:500-2000 ELISA 1:5000-20000serine peptidase inhibitor, Kunitz type 1(SPINT1) Homo sapiens The protein encoded by this gene is a member of the Kunitz family of serine protease inhibitors. The protein is a potent inhibitor specific for HGF activator and is thought to be involved in the regulation of the proteolytic activation of HGF in injured tissues. Alternative splicing results in multiple variants encoding different isoforms. [provided by RefSeq, Jul 2008],

SPIT2抗体应用：WB 1:500-2000 ELISA 1:5000-20000serine peptidase inhibitor, Kunitz type 2(SPINT2) Homo sapiens This gene encodes a transmembrane protein with two extracellular Kunitz domains that inhibits a variety of serine proteases. The protein inhibits HGF activator which prevents the formation of active hepatocyte growth factor. This gene is a putative tumor suppressor, and mutations in this gene result in congenital sodium diarrhea. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009],

SPN90抗体应用：WB 1:500-2000 ELISA 1:5000-20000NCK interacting protein with SH3 domain(NCKIPSD) Homo sapiens The protein encoded by this gene is localized exclusively in the cell nucleus. It plays a role in signal transduction, and may function in the maintenance of sarcomeres and in the assembly of myofibrils into sarcomeres. It also plays an important role in stress fiber formation. The gene is involved in therapy-related leukemia by a chromosomal translocation t(3;11)(p21;q23) that involves this gene and the myeloid/lymphoid leukemia gene. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013],

SPON1抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Cell adhesion protein that promotes the attachment of spinal cord and sensory neuron cells and the outgrowth of neurites in vitro. May contribute to the growth and guidance of axons in both the spinal cord and the PNS (By similarity). Major factor for vascular smooth muscle cell.,similarity:Contains 1 reelin domain.,similarity:Contains 1 spondin domain.,similarity:Contains 6 TSP type-1 domains.,subunit:Binds to the central extracellular domain of APP and inhibits beta-secretase cleavage of APP.,tissue specificity:Highest expression in lung, lower expression in brain, heart, kidney, liver and testis, and lowest expression in pancreas, skeletal muscle and ovary. Not expressed in spleen.,