TSACC抗体应用：WB 1:500-2000

TSG10抗体应用：WB 1:500-2000

TSH3抗体应用：WB 1:500-2000 ELISA 1:5000-20000teashirt zinc finger homeobox 3(TSHZ3) Homo sapiens This gene encodes a zinc-finger transcription factor that regulates smooth muscle cell differentiation in the developing urinary tract. Consistent with this role, mice in which this gene has been inactivated exhibit abnormal gene expression in urinary tract smooth muscle cell precursors and kidney defects including hydronephrosis. The encoded transcription factor comprises a gene silencing complex that inhibits caspase expression. Reduced expression of this gene and consequent caspase upregulation may be correlated with progression of Alzheimer's disease in human patients. [provided by RefSeq, Jul 2016],

TSHB抗体应用：WB 1:500-2000 ELISA 1:5000-20000thyroid stimulating hormone beta(TSHB) Homo sapiens The four human glycoprotein hormones chorionic gonadotropin (CG), luteinizing hormone (LH), follicle stimulating hormone (FSH), and thyroid stimulating hormone (TSH) are dimers consisting of alpha and beta subunits that are associated noncovalently. The alpha subunits of these hormones are identical, however, their beta chains are unique and confer biological specificity. Thyroid stimulating hormone functions in the control of thyroid structure and metabolism. The protein encoded by this gene is the beta subunit of thyroid stimulating hormone. Mutations in this gene are associated with congenital central and secondary hypothyroidism and Hashimoto's thyroiditis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013],

TSHR抗体应用：WB 1:500-2000 ELISA 1:5000-20000thyroid stimulating hormone receptor(TSHR) Homo sapiens The protein encoded by this gene is a membrane protein and a major controller of thyroid cell metabolism. The encoded protein is a receptor for thyrothropin and thyrostimulin, and its activity is mediated by adenylate cyclase. Defects in this gene are a cause of several types of hyperthyroidism. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008],

TSK抗体应用：WB 1:500-2000

TSN1抗体应用：WB 1:500-2000

TSP3抗体应用：WB 1:500-2000 ELISA 1:5000-20000thrombospondin 3(THBS3) Homo sapiens The protein encoded by this gene belongs to the thrombospondin family. Thrombospondin family members are adhesive glycoproteins that mediate cell-to-cell and cell-to-matrix interactions. This protein forms a pentameric molecule linked by a single disulfide bond. This gene shares a common promoter with metaxin 1. Alternate splicing results in coding and non-coding transcript variants. [provided by RefSeq, Nov 2011],

TSP50抗体应用：WB 1:500-2000 ELISA 1:5000-20000caution:Although related to peptidase S1 family, lacks the conserved active Ser residue in position 310 which is replaced by a Thr, suggesting that it has no protease activity.,miscellaneous:DNA hypomethylation is accompanied by the expression of the gene in the testis.,similarity:Belongs to the peptidase S1 family.,similarity:Contains 1 peptidase S1 domain.,tissue specificity:Testis specific. Differentially expressed in some breast cancer tissues.,

TSSC4抗体应用：WB 1:500-2000 ELISA 1:5000-20000tumor suppressing subtransferable candidate 4(TSSC4) Homo sapiens This gene is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene is located among several imprinted genes; however, this gene, as well as the pan-hematopoietic expression gene (PHEMX), escapes imprinting. This gene may play a role in malignancies and disease that involve this region. Several transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014],