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SETBP1 encodes a protein which contains a several motifs including a ski homology region and a SET-binding region in addition to three nuclear localization signals. Additionally we are shipping SETBP1 Proteins (4) and many more products for this protein.
Showing 10 out of 27 products:
Cow (Bovine) Polyclonal SETBP1 Primary Antibody for WB - ABIN2780976
Ott, Schmidt, Schwarzwaelder, Stein, Siler, Koehl, Glimm, Kühlcke, Schilz, Kunkel, Naundorf, Brinkmann, Deichmann, Fischer, Ball, Pilz, Dunbar, Du, Jenkins, Copeland, Lüthi, Hassan, Thrasher, Hoelzer, von Kalle, Seger, Grez: Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1. in Nature medicine 2006
Human Polyclonal SETBP1 Primary Antibody for IF, WB - ABIN525557
Filges, Shimojima, Okamoto, Röthlisberger, Weber, Huber, Nishizawa, Datta, Miny, Yamamoto: Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndrome. in Journal of medical genetics 2011
SETBP1 is a major oncogene (show RAB1A Antibodies) in myeloid neoplasms, which cooperates with various genetic events and causes distinct phenotypes of myelodysplastic/myeloproliferative neoplasms and secondary acute myeloid leukemia (show BCL11A Antibodies).
Results indicate a genotype-phenotype correlation in germline SET binding protein 1 (SETBP1) mutations spanning a molecular, cellular and clinical phenotype.
AML (show RUNX1 Antibodies) with RUNX1 (show RUNX1 Antibodies)/RUNX1T1 (show RUNX1T1 Antibodies) rearrangement displayed c.2903C>T alteration in the mutational hotspot of SETBP1.
Data describe a new recurrent chromosome translocation, t(12;18)(q14-q15;q12-21), in lipomas and osteochondrolipoma resulting in HMGA2-SETBP1 fusion which suggest a close developmental relationship between the two tumor types.
we described a patient not fulfilling the clinical criteria and showing mutation in SETBP1, we suggest that the facial gestalt associated with neurological involvement would be sufficient to indicate molecular analysis of this particular gene.
Correlation of myelodysplastic syndromes with i(17)(q10 (show EIF2C2 Antibodies)) and TP53 (show TP53 Antibodies) and SETBP1 mutations.
The SETBP1 and ASXL1 (show ASXL1 Antibodies) mutations have pathogenetic roles in CSF3R (show CSF3R Antibodies)-mutated chronic neutrophilic leukemia.
SETBP1 mutation might not be involved in the leukemogenisis of acute lymphoblastic leukemia
SETBP1 mutations are critical drivers of ASXL1 (show ASXL1 Antibodies)-mutated myelodysplastic syndrome.
mutation analysis of CSF3R (show CSF3R Antibodies), SETBP1 and CALR (show CALR Antibodies) should be included in the diagnostic criteria for chronic neutrophilic leukemia
We demonstrated that Nup98 (show NUP98 Antibodies)-TopIIbeta and Nup98 (show NUP98 Antibodies)-SETBP1 negatively regulate the XPO1 (show XPO1 Antibodies)-mediated protein export. Our results will contribute to the understanding of the molecular mechanism by which the Nup98 (show NUP98 Antibodies)-fusion proteins induce tumorigenesis.
Setbp1 overexpression also causes transcriptional repression of critical hematopoiesis regulator gene Runx1 (show RUNX1 Antibodies)
Setbp1 promotes the self-renewal of murine myeloid progenitors via activation of Hoxa9 (show HOXA9 Antibodies) and Hoxa10 (show HOXA10 Antibodies).
This gene encodes a protein which contains a several motifs including a ski homology region and a SET-binding region in addition to three nuclear localization signals. The encoded protein has been shown to bind the SET nuclear oncogene which is involved in DNA replication. Mutations in this gene are associated with Schinzel-Giedion midface retraction syndrome. Multiple transcript variants encoding different isoforms have been found for this gene.
A20-binding inhibitor of NF-kappaB activation 2
, SET binding protein 1
, SET-binding protein-like
, SET-binding protein