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FOXD3 (C-20) Antibody: sc-27888

 |  Datasheet
  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping at the C-terminus of FOXD3 of human origin
  • recommended for detection of FOXD3 of mouse, rat and human origin by WB, IF and ELISA; also reactive with additional species, including bovine
  • blocking peptide, sc-27888 P
  • TransCruz reagent for Gel Supershift and ChIP applications, sc-27888 X, 200 µg/0.1 ml
 
Additional FOX Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IF   Gel Shift   ChIP   siRNA  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human FOXD3 27022 1p31.3 NM_012183 Q9UJU5
611539
Mouse Foxd3 15221 4 C6 Q61060
N/A
 
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 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
FOXD3 (C-20) sc-27888 200 µg/ml $279
FOXD3 (C-20) P sc-27888 P
(peptide)
100 µg/0.5 ml $61
FOXD3 (C-20) X sc-27888 X 200 µg/0.1 ml $279
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
FOXD3 siRNA (h) sc-43768 10 µM $258
FOXD3 siRNA (m) sc-145222 10 µM $258
FOXD3 (h)-PR sc-43768-PR 10 µM $23
FOXD3 (m)-PR sc-145222-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
FOXD3 shRNA Plasmid (h) sc-43768-SH 20 µg $520
FOXD3 shRNA Plasmid (m) sc-145222-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
FOXD3 shRNA (h) Lentiviral Particles sc-43768-V 200 µl $625
FOXD3 shRNA (m) Lentiviral Particles sc-145222-V 200 µl $625

FOXD3 Background Information
Embryonic stem cells require the forkhead transcriptional regulator FoxD3 for survival. Following gastrulation, FoxD3 generally gets downregulated, except in the neural crest. A variety of growth factors induce FoxD3 expression, including FGF8 and SNAIL, maintaining the effected cells in an undifferentiated state. Thus defects in FoxD3 induction may cause premature differentiation and/or migration-asociated birth defects.