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STAG3 (A-15) Antibody: sc-23628

 |  Datasheet
  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping near the N-terminus of STAG3 of human origin
  • recommended for detection of STAG3 of human origin by WB, IF and ELISA
  • blocking peptide, sc-23628 P
 
Additional STAG Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IF   siRNA  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human STAG3 10734 7q22.1 NM_012447 Q9UJ98
608489
 
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
STAG3 (A-15) sc-23628 200 µg/ml $279
STAG3 (A-15) P sc-23628 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
STAG3 siRNA (h) sc-38451 10 µM $258
STAG3 (h)-PR sc-38451-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
STAG3 shRNA Plasmid (h) sc-38451-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
STAG3 shRNA (h) Lentiviral Particles sc-38451-V 200 µl $625

STAG3 Background Information
Stromalins are a group of highly conserved proteins that are characterized by the stromalin conservative domain. Stromal antigen 3 (STAG3) is a nuclear protein that is expressed specifically in germinal cells. STAG3 associates with the synaptonemal complex (SC) via immunolocalization. The SC is a meiotic protein structure that aids in the pairing of homologous chromosomes. In mammals, STAG3 associates with the SC and assists in sister chromatid cohesion, which keeps the homologous chromosomes appropriately aligned during the pachytene stage of prophase I. STAG3 appears to be located at the interchromatid domain during metaphase I, but is undetectable in ana-phase I or any of the later stages of meiosis. The human STAG3 gene maps to 7q22. There have been six additional STAG3-related genes mapped in humans. Two of these genes flank the chromosomal breakpoints associated with the Williams-Beuren syndrome (WBS), a microdeletion syndrome with varied clinical presentations.