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MEIS2 encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins. Additionally we are shipping MEIS2 Proteins (6) and many more products for this protein.
Showing 10 out of 90 products:
Human Monoclonal MEIS2 Primary Antibody for IF, IHC (p) - ABIN561794
García-Moreno, Pedraza, Di Giovannantonio, Di Salvio, López-Mascaraque, Simeone, De Carlos: A neuronal migratory pathway crossing from diencephalon to telencephalon populates amygdala nuclei. in Nature neuroscience 2010
Show all 3 references for ABIN561794
Chicken Polyclonal MEIS2 Primary Antibody for IHC, WB - ABIN2775951
Yang, Hwang, DSouza, Lee, Junn, Mouradian: Three-amino acid extension loop homeodomain proteins Meis2 and TGIF differentially regulate transcription. in The Journal of biological chemistry 2000
Show all 2 references for ABIN2775951
Chicken Polyclonal MEIS2 Primary Antibody for WB - ABIN2775124
Shim, Kim, Shin, Kim, Park: Regulation of EphA8 gene expression by TALE homeobox transcription factors during development of the mesencephalon. in Molecular and cellular biology 2007
Human Polyclonal MEIS2 Primary Antibody for ICC, IF - ABIN4333477
He, Ebarasi, Zhao, Guo, Ojala, Hultenby, De Val, Betsholtz, Tryggvason: Lmx1b and FoxC combinatorially regulate podocin expression in podocytes. in Journal of the American Society of Nephrology : JASN 2014
Human Polyclonal MEIS2 Primary Antibody for ELISA, WB - ABIN4333476
Mercader, Leonardo, Azpiazu, Serrano, Morata, Martínez, Torres: Conserved regulation of proximodistal limb axis development by Meis1/Hth. in Nature 1999
we have identified a novel nonsense MEIS2 mutation in a female patient with cleft palate, cardiac septal defect, severe ID, developmental delay and feeding difficulty with gastro-esophageal reflux. Our findings strongly suggest neurocristopathy be included in the clinical features associated with MEIS2 alterations.
Meis2 as the target of miR (show MLXIP Antibodies)-134 in the regulation of cardiomyocyte progenitor cell proliferation.
This is the first report showing a de novo small intragenic mutation in MEIS2 and further confirms the important role of this gene in normal development.
Our results show that MEIS2 is a gene needed for palate closure. In syndromic cases of cleft palate, MEIS2 should be considered among the candidate genes, for example, in cases without 22q11.2 deletions.
FOXM1 (show FOXM1 Antibodies) is a direct target gene of MEIS2 and is required for MEIS2 to upregulate mitotic genes.
The data suggest existence of a complex regulatory pathway in the trabecular meshwork part of which includes interactions between FOXC1 (show FOXC1 Antibodies), miR (show MLXIP Antibodies)-204, MEIS2, and ITGbeta1.
Klf4 (show KLF4 Antibodies) recruits a complex of Meis and Pbx proteins to DNA, resulting in Meis2 transcriptional activation domain-dependent activation of a subset of Klf4 (show KLF4 Antibodies) target genes.
The Single Nucleotide Polymorphism in Meis homeobox 2 (MEIS2) mediated the effects of risperidone on hip circumference (q=0.004).
Transgenic mice lacking microRNAs miR (show MLXIP Antibodies)-9-2 and miR (show MLXIP Antibodies)-9-3 exhibit multiple defects of telencephalic structures which may be brought about by dysregulation of Foxg1 (show FOXG1 Antibodies), Nr2e1 (show NR2E1 Antibodies), Gsh2 (show GSX2 Antibodies), and Meis2 expression.
Data demonstrate by in situ hybridization and immunohistochemistry that the two homeobox (show Lbx1 Antibodies) genes Pax6 (show PAX6 Antibodies) and MEIS2 are expressed during early fetal brain development in humans.
Meis2-null mice are embryonic lethal. The results reveal a critical role of Meis2 during cranial and cardiac neural crest cells development in mouse.
Data suggest that the RING1 (show RING1 Antibodies)-MEIS1 (show MEIS1 Antibodies)/2 axis is regulated by early PD signals and contributes to the initiation or maintenance of the distal signal circuitry.
Interaction of Meis2 promoter with midbrain enhancer depends on RING1.
Meis2 cooperates with Pax6 (show PAX6 Antibodies) in generic neurogenesis and dopaminergic fate specification in the adult subventricular zone-olfactory bulb system.
These data identify Meis2 as a marker for the study of amacrine cell diversity and development in addition to providing evidence for the stepwise specification of the glycinergic and GABAergic neurotransmitter phenotypes during AM cell differentiation.
Retinal progenitor cells (RPCs) in chicks and mice express two Hth-related proteins, Meis1 (show MEIS1 Antibodies) and Meis2.
This gene encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins. TALE homeobox proteins are highly conserved transcription regulators, and several members have been shown to be essential contributors to developmental programs. Multiple transcript variants encoding distinct isoforms have been described for this gene.
Meis homeobox 2
, homeobox protein Meis2-like
, homeobox protein Meis2
, myeloid ecotropic viral integration site 2.2
, XMeis1-3 protein
, Meis1, myeloid ecotropic viral integration site 1 homolog 2
, homeoprotein Meis2a.1
, homeoprotein Meis2a.2
, myeloid ecotropic viral insertion site-2a protein
, Meis homolog 2
, Meis1-related gene 1
, TALE homeobox protein Meis2
, meis1-related protein 1
, Cbp/p300-interacting transactivator with Glu/Asp-rich carboxy-terminal domain 2
, myeloid ecotropic viral integration site-related gene 1
, myeloid ecotropic viral integration site 2.1