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MEOX1 encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. Additionally we are shipping MEOX1 Proteins (9) and many more products for this protein.
Showing 10 out of 75 products:
Human Polyclonal MEOX1 Primary Antibody for EIA, WB - ABIN359497
Vatanavicharn, Graham, Curry, Pepkowitz, Lachman, Rimoin, Wilcox: Diaphanospondylodysostosis: six new cases and exclusion of the candidate genes, PAX1 and MEOX1. in American journal of medical genetics. Part A 2007
Show all 3 references for ABIN359497
Human Polyclonal MEOX1 Primary Antibody for EIA, WB - ABIN783739
Candia, Wright: Differential localization of Mox-1 and Mox-2 proteins indicates distinct roles during development. in The International journal of developmental biology 1997
Show all 2 references for ABIN783739
Cow (Bovine) Polyclonal MEOX1 Primary Antibody for IHC, WB - ABIN2777534
Jones, Black, Brown, Griffiths, Nicolai, Chambers, Bonjardim, Xu, Boyd, McFarlane: The detailed characterisation of a 400 kb cosmid walk in the BRCA1 region: identification and localisation of 10 genes including a dual-specificity phosphatase. in Human molecular genetics 1995
Human Polyclonal MEOX1 Primary Antibody for WB - ABIN1881549
Petropoulos, Gianakopoulos, Ridgeway, Skerjanc: Disruption of Meox or Gli activity ablates skeletal myogenesis in P19 cells. in The Journal of biological chemistry 2004
study reveals the molecular basis for a novel somite lineage restriction mechanism (controlled by meox1) and defines a new paradigm in induction of definitive hematopoietic stem cells
The G > A p.Q84X mutation in the MEOX1 is identified in Klippel-Feil syndrome (show GDF6 Antibodies).
We describe a multiplex consanguineous family in which isolated KFS (show GDF6 Antibodies) maps to a single 17q21.31 locus that harbors a homozygous frameshift deletion in MEOX1; this deletion results in complete instability of the transcript
The results demonstrate that MEOX1 is a critical target gene and cofactor of PBX1 (show PBX1 Antibodies) in ovarian cancers.
No mutations were identified in the PAX1 (show PAX1 Antibodies) and MEOX1 exons or flanking intronic sequences, excluding them as likely causative genes for diaphanospondylodysostosis
MEOX1 and MEOX2 (show MEOX2 Antibodies) activate p16(INK4a (show CDKN2A Antibodies)) in a DNA binding dependent manner, whereas they induce p21(CIP1/WAF1 (show CDKN1A Antibodies)) in a DNA binding independent manner.
Meox1 expression is downregulated in the second arch of Hoxa2 (show HOXA2 Antibodies) mouse mutant embryos.
Results demonstrate that Meox1 and Meox2 (show MEOX2 Antibodies) genes function together and upstream of several genetic hierarchies that are required for the development of somites.
Data show that Meox1 activates the Bapx1 (show NKX3-2 Antibodies) promoter in a dose-dependent manner and that this activity is enhanced in the presence of Pax1 (show PAX1 Antibodies) and/or Pax9 (show PAX9 Antibodies).
Meox and Gli (show GLI1 Antibodies) have roles in skeletal myogenesis
Data sugges that Meox1 is part of a regulatory circuit that serves an essential, non-redundant function in the maintenance of rostro-caudal (show CAD Antibodies) sclerotome polarity and axial skeleton formation.
This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the molecular signaling network regulating somite development. Alternatively spliced transcript variants encoding different isoforms have been described.
Mox-1 related protein
, homeobox protein MOX-1
, mesenchyme homeo box 1
, mesenchyme homeobox 1
, Homeobox protein MOX-1