santa cruz biotechnology, inc.
SCBT Logo

Welcome!        Items in Cart     Quick Order

Mds1 (N-20) Antibody: sc-48274

 |  Datasheet
  • goat polyclonal IgG, 200µg/ml
  • epitope mapping at the N-terminus of Mds1 of human origin
  • recommended for detection of Mds1 and Mds1-Evi-1 fusion protein of human origin by WB, IF and ELISA; also reactive with additional species, including equine and porcine
  • TransCruz reagent for Gel Supershift and ChIP applications, sc-48274 X, 200 µg/0.1 ml
  • blocking peptide, sc-48274 P
 
Additional EVI Antibodies ...
 
Ordering Information
Recommended Support Products:
(click button of application of choice)
WB   IF   Gel Shift   ChIP  
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human MDS1 4197 3q26.2 NM_004991 Q13465
n/a
Mouse Mds1 17251 3 A3 Q9Z1L8
N/A
 
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
Mds1 (N-20) sc-48274 200 µg/ml $279
Mds1 (N-20) P sc-48274 P
(peptide)
100 µg/0.5 ml $61
Mds1 (N-20) X sc-48274 X 200 µg/0.1 ml $279

Evi-1 Background Information
The Mds1 and Evi-1 genes located on human chromosome 3q26.2 form a complex locus that encodes three different proteins: Mds1, Evi-1 and a Mds1-Evi-1 fusion protein. Mds1 is a 169 amino acid protein that has lower expression levels than either Mds1-Evi-1 fusion protein or Evi-1. The Mds1-Evi-1 fusion protein is expressed in both normal and leukemic tissues and contains several zinc finger domains. Evi-1 contains two zinc finger domains, the second of which is essential for transactivation of the c-Fos promoter and for AP-1 activation. The first zinc finger domain in Evi-1 binds to Smad3, suppressing its activity and inhibiting TGF∫ signaling. The t(3;21) (q26;q22) chromosomal translocation of Evi-1 produces a chimeric transcription factor, AML-1/Evi-1, that appears to suppress the transactivation of AML-1, which is a stimulator of myeloid cell differentiation. Inappropriate Evi-1 gene expression in hemato-poietic cells has been shown to be associated with acute myelogenous leukemia (AML) and myelodysplastic syndromes.