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anti-Mouse (Murine) WNT1 Antikörper:
anti-Human WNT1 Antikörper:
anti-Rat (Rattus) WNT1 Antikörper:
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Human Polyclonal WNT1 Primary Antibody für IF (p), IHC (p) - ABIN733748
Gao, Liu, Chen, Lv, Wu, Mi, Wang: Comparative study of Hsp27, GSK3?, Wnt1 and PRDX3 in Hirschsprung's disease. in International journal of experimental pathology 2014
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Human Polyclonal WNT1 Primary Antibody für WB - ABIN3042350
Dong, Duan, Han, Zhang, Wu: Suppression of wingless-type MMTV integration site family, member 1 expression by small interfering RNA inhibits U251 glioma cell growth in vitro. in Oncology letters 2014
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Human Monoclonal WNT1 Primary Antibody für ICC, FACS - ABIN969458
Toffart, Moro-Sibilot, Couraud, Merle, Perol, Girard, Souquet, Mastroianni, Ferretti, Romand, Chatellain, Vesin, Brambilla, Brambilla, Timsit: Evaluation of RECIST in chemotherapy-treated lung cancer: the Pharmacogenoscan Study. in BMC cancer 2015
maternal Wnt (zeige WNT2 Antikörper)/STOP signaling, but not beta-catenin (zeige CTNNB1 Antikörper) signaling, has a role in cleavage after fertilization and cell cycle progression
sfrp1 (zeige SFRP1 Antikörper) promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt (zeige WNT2 Antikörper) signalling.
analysis of differential role of Axin (zeige AXIN1 Antikörper) RGS (zeige PITX2 Antikörper) domain function in Wnt (zeige WNT2 Antikörper) signaling during anteroposterior patterning and maternal axis formation
Data show taht combined Wnt (zeige WNT2 Antikörper) and Nodal signaling synergistically activates transcription of Spemann organizer genes.
The authors propose that these dual functions of DP1 (zeige TFDP1 Antikörper) can promote and stabilize biphasic Wnt (zeige WNT2 Antikörper)-on and Wnt (zeige WNT2 Antikörper)-off states in response to a gradual gradient of Wnt (zeige WNT2 Antikörper)/beta-catenin (zeige CTNNB1 Antikörper) signalling to determine differential cell fates.
Pax9 (zeige PAX9 Antikörper)-dependent Wnt (zeige WNT2 Antikörper) signaling has a role in palatogenesis and cleft palates
Data show that autocrine Wnt (zeige WNT2 Antikörper) secretion is important for the survival, chromosomal stability, differentiation, and tumorigenic potential of embryonic stem cells (ESCs (zeige NR2E3 Antikörper)).
Results demonstrated functional differences in the molecular mechanisms downstream of Wnt1 function in the diencephalon, in relation to the spinal cord. Wnt1 signal determines the patterning of the diencephalic dorso-ventral axis
Data show that both transgenic Wnt1-cre and P0-cre are similarly effective in deleting beta-catenin (zeige CTNNB1 Antikörper) in the neural crest.
data suggest that WNT1-related osteogenesis imperfecta (zeige COL1A2 Antikörper) and osteoporosis are caused in part by decreased mTORC1-dependent osteoblast function resulting from loss of WNT1 signaling in osteocytes.
Administration of EET alters Wnt1, NOV (zeige NOV Antikörper), and HO-1 (zeige HMOX1 Antikörper) signaling to prevent obesity-induced cardiomyopathy in obese mice.
Data indicate that Wnt1 proto-oncogene (zeige RAB1A Antikörper) protein (WNT1) is the direct target of microRNA miR (zeige MLXIP Antikörper)-34a in dendritic cell (DC).
In order to evaluate the function of IFT88 (zeige IFT88 Antikörper) in regulating craniofacial development, we generated Wnt1-Cre;Ift88fl/fl mice to eliminate Ift88 (zeige IFT88 Antikörper) specifically in cranial neural crest (CNC) cells. Wnt1-Cre;Ift88fl/flpups died at birth due to severe craniofacial defects including bilateral cleft lip and palate and tongue agenesis, following the loss of the primary cilia in the CNC-derived palatal mesenchyme
Wnt (zeige WNT2 Antikörper), Eda (zeige EDA Antikörper), and Shh (zeige SHH Antikörper) have roles in touch dome Merkel cell development
The data obtained from the 14-3-3epsilon/14-3-3zeta (zeige YWHAZ Antikörper)/Wnt1-Cre mice strongly indicate the importance of 14-3-3 (zeige YWHAQ Antikörper) proteins in the development of melanocyte lineages.
WNT1 osteoporosis causes significant skeletal changes already in early childhood and impairs bone mass gain during pubertal years.
High WNT1 expression is associated with esophageal squamous cell carcinoma.
High WNT1 expression in stromal cells is associated with myelodysplastic syndrome.
High WNT1 expression is associated with gastric cancer.
Novel compound heterozygous WNT1 missense mutations, p.Glu123Asp and p.Cys153Gly, identified in a patient with osteogenesis imperfecta (zeige COL1A2 Antikörper).
Osteocyte protein expression is altered in patients with osteoporosis caused by WNT1 mutation.
High WNT1 expression is associated with glioma cell invasion.
bone formation is under the control of WNT1 produced by osteocytes, the cells that reside deep in the bone matrix and form dendritic networks.
Knocking down of Wnt-1 by siRNA had the similar effect of miRNA-148a overexpression on cell migration and invasion in lung cancer cells.
High WNT1 expression is associated with Lung Adenocarcinoma Progression.
Data indicate that Wnt-1 protein is present in postdevelopmental endothelial cells where it associates with cytoskeletal elements and may retain function as a tissue polarity gene.
Rspo1-Wnt-VegfC-Vegfr3 signaling plays a crucial role as an endothelial-autonomous permissive cue for developmental angiogenesis.
wnt1 and wnt10b (zeige WNT10B Antikörper) are required to maintain threshold levels of Pax2.1 and Fgf8 (zeige FGF8 Antikörper) at the midbrain-hindbrain boundary.
novel role for Wnt (zeige WNT2 Antikörper)/beta-catenin (zeige CTNNB1 Antikörper) signalling in determining endocardial cell fate
In zebrafish embryos lacking Wnt3a (zeige WNT3A Antikörper), Wnt1 and Wnt10b (zeige WNT10B Antikörper), the expression of engrailed orthologs, pax2a and fgf8 (zeige FGF8 Antikörper) is not maintained after mid-somitogenesis
two Dvl (zeige DVL2 Antikörper)-associated paralogs, Dpr1 (zeige DACT1 Antikörper) and Dpr2 (zeige DACT2 Antikörper), participate in distinct Wnt (zeige WNT2 Antikörper)-dependent developmental processes
Wnt (zeige WNT2 Antikörper)/Axin (zeige AXIN1 Antikörper)/beta-catenin (zeige CTNNB1 Antikörper) pathway has a role in ventral CNS development
The boundary and roof plate expression of wnt1 each contribute to upregulation of proneural and delta gene expression and neurogenesis in non-boundary regions.
Epistatic analyses suggest a possible genetic interaction between Wnt (zeige WNT2 Antikörper)/beta-catenin (zeige CTNNB1 Antikörper) and Myostatin (zeige MSTN Antikörper) in regulation of slow and fast twitch muscle myofibrillogenesis
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.
, protein Wnt-1
, proto-oncogene Int-1
, proto-oncogene Wnt-1
, proto-oncogene protein Wnt-1
, proto-oncogene Int-1 homolog
, wingless-type MMTV integration site family, member 1 (oncogene INT1)
, Wingless-type MMTV integration site 1 homolog
, Wingless-type MMTV integration site 1, homolog
, wingless-related MMTV integration site 1
, murine mammary tumor virus integration site
, wingless-type MMTV integration site family member 1