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SSX (N-16) Antibody: sc-8818

 |  Datasheet
  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping at the N-terminus of SSX2 of human origin
  • recommended for detection of SSX2, SSX2B, SSX3, SSX5, SSX7, SSX9 and, to a lesser extent, SSX4 of human origin by WB, IP, IF and ELISA
  • blocking peptide, sc-8818 P
  • TransCruz reagent for Gel Supershift and ChIP applications, sc-8818 X, 200 µg/0.1 ml
 
Additional SSX Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IP   IF   Gel Shift   ChIP  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human SSX2 6757 Xp11.22 NM_003147, NM_175698 Q16385
300192
Human SSX3 10214 Xp11.23 NM_021014, NM_175711 Q99909
300325
Human SSX2B 727837 Xp11.22 XM_001125936 Q16385
 
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
SSX (N-16) sc-8818 200 µg/ml $279
SSX (N-16) P sc-8818 P
(peptide)
100 µg/0.5 ml $61
SSX (N-16) sc-8818 X 200 µg/0.1 ml $279
 WB Positive Control Cell Lysates (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
SSX (h2): 293T Lysate sc-112491 100µg/200µl $205
HeLa Whole Cell Lysate sc-2200 500 µg/200 µl $104

SSX Background Information
The transcriptional coactivator SYT (synovial translocation protein) contains a conserved amino terminal SNH domain and a carboxy terminal QPGY domain, which is a functioning transcriptional activating sequence. Synovial sarcoma translocation (SSX) proteins, including SSX1-5, are transcriptional repressors that contain a repressor domain in their carboxy termini. SSX proteins are localized to the nucleus and expressed in testis and several types of cancers and, therefore, they are classified as C/T (cancer/testis) antigens. The t(x;18) translocation results in the fusion of the amino terminus of SYT to the carboxy terminus of either SSX1 or SSX2; both fusions result in the production of transcriptional activators. SYT-SSX chimeras are detected in most synovial sarcomas. Synovial sarcomas are responsible for up to 10% of soft issue sarcomas and are histologically characterized as either biphasic or monophasic. Genetic analysis indicates that biphasic synovial sarcomas contain SYT-SSX1 fusions, whereas SYT-SSX2 fusions are found in monophasic synovial sarcomas, providing additional distinguishing characterization of these subtypes.