SIR4抗体应用：WB 1:500-2000 ELISA 1:5000-20000sirtuin 4(SIRT4) Homo sapiens This gene encodes a member of the sirtuin family of proteins, homologs to the yeast Sir2 protein. Members of the sirtuin family are characterized by a sirtuin core domain and grouped into four classes. The functions of human sirtuins have not yet been determined; however, yeast sirtuin proteins are known to regulate epigenetic gene silencing and suppress recombination of rDNA. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity. The protein encoded by this gene is included in class IV of the sirtuin family. [provided by RefSeq, Jul 2008],

SIVA抗体应用：WB 1:500-2000 ELISA 1:5000-20000SIVA1 apoptosis inducing factor(SIVA1) Homo sapiens This gene encodes a protein with an important role in the apoptotic (programmed cell death) pathway induced by the CD27 antigen, a member of the tumor necrosis factor receptor (TFNR) superfamily. The CD27 antigen cytoplasmic tail binds to the N-terminus of this protein. Two alternatively spliced transcript variants encoding distinct proteins have been described. [provided by RefSeq, Jul 2008],

SIX3抗体应用：WB 1:500-2000 ELISA 1:5000-20000SIX homeobox 3(SIX3) Homo sapiens This gene encodes a member of the sine oculis homeobox transcription factor family. The encoded protein plays a role in eye development. Mutations in this gene have been associated with holoprosencephaly type 2. [provided by RefSeq, Oct 2009],

SIX4抗体应用：WB 1:500-2000 ELISA 1:5000-20000SIX homeobox 4(SIX4) Homo sapiens This gene encodes a member of the homeobox family, subfamily SIX. The drosophila homolog is a nuclear homeoprotein required for eye development. Studies in mouse show that this gene product functions as a transcription factor, and may have a role in the differentiation or maturation of neuronal cells. [provided by RefSeq, May 2010],

SKAP1抗体应用：WB 1:500-2000 ELISA 1:5000-20000src kinase associated phosphoprotein 1(SKAP1) Homo sapiens This gene encodes a T cell adaptor protein, a class of intracellular molecules with modular domains capable of recruiting additional proteins but that exhibit no intrinsic enzymatic activity. The encoded protein contains a unique N-terminal region followed by a PH domain and C-terminal SH3 domain. Along with the adhesion and degranulation-promoting adaptor protein, the encoded protein plays a critical role in inside-out signaling by coupling T-cell antigen receptor stimulation to the activation of integrins. [provided by RefSeq, Jul 2008],

SKI抗体应用：WB 1:500-2000 ELISA 1:5000-20000SKI proto-oncogene(SKI) Homo sapiens This gene encodes the nuclear protooncogene protein homolog of avian sarcoma viral (v-ski) oncogene. It functions as a repressor of TGF-beta signaling, and may play a role in neural tube development and muscle differentiation. [provided by RefSeq, Oct 2009],

SKOR1抗体应用：WB 1:500-2000

SL9A1抗体应用：WB 1:500-2000 ELISA 1:5000-20000solute carrier family 9 member A1(SLC9A1) Homo sapiens This gene encodes a Na+/H+ antiporter that is a member of the solute carrier family 9. The encoded protein is a plasma membrane transporter that is expressed in the kidney and intestine. This protein plays a central role in regulating pH homeostasis, cell migration and cell volume. This protein may also be involved in tumor growth. [provided by RefSeq, Sep 2011],

SL9A2抗体应用：WB 1:500-2000 ELISA 1:5000-20000solute carrier family 9 member A2(SLC9A2) Homo sapiens This gene encodes a member of the sodium-hydrogen exchanger (NHE) protein family. These proteins are involved in sodium-ion transport by exchanging intracellular hydrogen ions to external sodium ions and help in the regulation of cell pH and volume. The encoded protein is localized to the apical membrane and is involved in apical absorption of sodium. [provided by RefSeq, Jun 2016],

SL9A3抗体应用：WB 1:500-2000 ELISA 1:5000-20000solute carrier family 9 member A3(SLC9A3) Homo sapiens The protein encoded by this gene is an epithelial brush border Na/H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in this gene are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22. [provided by RefSeq, Mar 2016],