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抗Human LHX2 抗体:
抗Rat (Rattus) LHX2 抗体:
抗Mouse (Murine) LHX2 抗体:
Human Polyclonal LHX2 Primary Antibody for ELISA, WB - ABIN409082
Mangale, Hirokawa, Satyaki, Gokulchandran, Chikbire, Subramanian, Shetty, Martynoga, Paul, Mai, Li, Flanagan, Tole, Monuki: Lhx2 selector activity specifies cortical identity and suppresses hippocampal organizer fate. in Science (New York, N.Y.) 2008
Goat Polyclonal LHX2 Primary Antibody for IF (p), IHC (p) - ABIN1387858
Geng, Wang, Wang, Chen: Cyclic expression of Lhx2 is involved in secondary hair follicle development in cashmere goat. in Gene expression patterns : GEP 2014
Findings demonstrate that miR (显示 MLXIP 抗体)-1238 inhibit the proliferation of NSCLC cells at least partly via repression of LHX2, shedding light on the mechanistic interaction of miR (显示 MLXIP 抗体)-1238 and LHX2 in NSCLC carcinogenesis.
Results show that LHX2 is overexpressed in pancreatic ductal adenocarcinoma cells and is involved in promoting cancer cell proliferation and enhanced tumor development.
Lhx2 directly regulates tanycyte specification and differentiation in the hypothalamus.
This study demonistrated that LHx2 regulates the development of the forebrain hem system.
The data indicate a dual role of Lhx2 during EMT (显示 ITK 抗体) and tumor progression: by inducing the expression of PDGF-B (显示 PDGFB 抗体), Lhx2 provokes an autocrine PDGF-B (显示 PDGFB 抗体)/PDGFRbeta loop required for cell migration, invasion and metastatic dissemination
The findings indicate that LHX2 regulates the transcription of downstream intrinsic and extrinsic molecules that are essential for early neural differentiation.
These results suggest that if LHX2 is involved in pituitary hormone (显示 CGA 抗体) deficiency associated with posterior pituitary and ocular defects, it would be a rare cause of this disease condition.
Mutations in LHX2 do not represent a frequent cause of micro/anophthalmia.
A large cohort of patients with schizencephaly, some with features of septo-optic dysplasia, were sequenced for mutations in LHX2, HESX1 (显示 HESX1 抗体) and SOX2 (显示 SOX2 抗体).
Lack of Lhx2/Lhx9 (显示 LHX9 抗体) function as well as increased Wnt (显示 WNT2 抗体) signaling alter the expression of the thalamus specific cell adhesion factor pcdh10b and lead subsequently to a striking anterior-posterior disorganization of the caudal (显示 CAD 抗体) forebrain.
Lhx2 may mediate an alternative or parallel pathway for control of cellular proliferation in the developing forebrain via Six3.
Lhx2 regulates Dmrt5 (显示 DMRTA2 抗体): loss of either factor promotes gliogenesis and overexpression of either factor promotes neurogenesis.
Neuroretinal expression of Lhx2 and neuroretina-derived FGF factors are crucial for lens fiber development in vivo.
LHX2 is a key component of the control network for producing neurons that will participate in cortical circuitry
We found that expression of Emx2 (显示 EMX2 抗体) and Lhx2 initiated between neuronal progenitor and neuronal precursor stages. As far as the sensory neurons of the vomeronasal organ are concerned, Meis1 (显示 MEIS1 抗体) and Meis2 (显示 MEIS2 抗体) were only expressed in the apical layer, together with Gnai2 (显示 GNAI2 抗体), but not in the basal layer.
Lhx2 is required for maintenance of the corneal epithelial cell compartment and the limbal barrier.
The ectopic expression of Lhx2 in OP9 cells (OP9-Lhx2) accelerates the hematopoietic differentiation of PSCs.
Conditional knock-out of Lhx2 resulted in down-regulation of Notch (显示 NOTCH1 抗体) pathway genes in retinal glia.
These studies define essential roles for Lhx2 in glial wedge, hippocampal commissure, and corpus callosum formation, and suggest that defects in radial glial wedge progenitors can give rise to corpus callosum.
CTIP2 (显示 BCL11B 抗体) transcription factor maintains stem cells in hair follicle and alters LHX2 expression.
Lhx2 regulates the timing of beta-catenin (显示 CTNNB1 抗体)-dependent cortical neurogenesis.
Lhx2 expression during porcine fetal and postnatal pituitary development showed a gradual increase from fetal day (f) 40 to postnatal day (p) 8 followed by a slight decrease to p230 (显示 TNC 抗体).
This gene encodes a protein belonging to a large protein family, members of which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator. The protein can recapitulate or rescue phenotypes in Drosophila caused by a related protein, suggesting conservation of function during evolution.
LIM HOX gene 2
, LIM homeobox protein 2
, LIM/homeobox protein Lhx2
, homeobox protein LH-2
, LIM homeodomain
, LIM homeobox 2
, LIM homeodomain type transcription factor Lhx2
, LIM homeo box protein 2