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anti-Human ARNTL Antikörper:
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Human Polyclonal ARNTL Primary Antibody für ChIP, ICC - ABIN151688
Hayashida, Kuramoto, Koyanagi, Oishi, Fujiki, Matsunaga, Ikeda, Ohdo, Shimeno, Soeda: Proxisome proliferator-activated receptor-α mediates high-fat, diet-enhanced daily oscillation of plasminogen activator inhibitor-1 activity in mice. in Chronobiology international 2010
Show all 11 Pubmed References
Human Monoclonal ARNTL Primary Antibody für IHC, ELISA - ABIN968967
Motzkus, Loumi, Cadenas, Vinson, Forssmann, Maronde: Activation of human period-1 by PKA or CLOCK/BMAL1 is conferred by separate signal transduction pathways. in Chronobiology international 2007
Show all 3 Pubmed References
Human Monoclonal ARNTL Primary Antibody für IHC, ELISA - ABIN965595
Lee, Lee, Lee, Park, Kang, Chung, Lee, Kim: Dual modification of BMAL1 by SUMO2/3 and ubiquitin promotes circadian activation of the CLOCK/BMAL1 complex. in Molecular and cellular biology 2008
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Human Polyclonal ARNTL Primary Antibody für ELISA, WB - ABIN449912
Fuller, Lu, Saper: Differential rescue of light- and food-entrainable circadian rhythms. in Science (New York, N.Y.) 2008
Polyclonal ARNTL Primary Antibody für ChIP, IP - ABIN540781
Oishi, Sakamoto, Okada, Nagase, Ishida: Antiphase circadian expression between BMAL1 and period homologue mRNA in the suprachiasmatic nucleus and peripheral tissues of rats. in Biochemical and biophysical research communications 1999
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Human Monoclonal ARNTL Primary Antibody für FACS, IF - ABIN2452787
Trejo-Muñoz, Navarrete, Montúfar-Chaveznava, Caldelas: Temporal modulation of the canonical clockwork in the suprachiasmatic nucleus and olfactory bulb by the mammary pheromone 2MB2 in pre-visual rabbits. in Neuroscience 2014
NR1D1 (zeige NR1D1 Antikörper) and BMAL1 mRNA and protein levels were significantly reduced in OA compared to normal cartilage. In cultured human chondrocytes, a clear circadian rhythmicity was observed for NR1D1 (zeige NR1D1 Antikörper) and BMAL1.
These results suggest that the circadian clock system can be recovered through BMAL1 expression induced by aza-dC within a day.
Determined a novel role of TNF-alpha (zeige TNF Antikörper) in inducing Bmal1 via dual calcium dependent pathways; Roralpha was up-regulated in the presence of Ca(2 (zeige CA2 Antikörper)+) influx and Rev-erbalpha (zeige NR1D1 Antikörper) was down-regulated in the absence of that.
results of this study suggest that genetic variability in the ARNTL and CLOCK genes might be associated with risk for multiple sclerosis
PI3K (zeige PIK3CA Antikörper)-PTEN upregulated-mTORC1 and mTORC2 (zeige CRTC2 Antikörper) complex plays a critical role in controlling BMAL1, establishing a connection between PI3K (zeige PIK3CA Antikörper) signaling and the regulation of circadian rhythm, ultimately resulting in deregulated BMAL1 in tumor cells with disrupted PI3K (zeige PIK3CA Antikörper) signaling
M. tuberculosis infection caused enhanced MMP-1 (zeige MMP1 Antikörper), -9, and miR (zeige MLXIP Antikörper)-223 expression, with inhibited BMAL1 expression. MiR (zeige MLXIP Antikörper)-223 modulated BMAL1 expression via the direct binding of BMAL1 3'-UTR (zeige UTS2R Antikörper).
research describes an association between changes in the methylation of the BMAL1 gene with the intervention and the effects of a weight loss intervention on blood lipids levels
Study found rhythmic methylation of BMAL1 was altered in Alzheimer's disease brains and fibroblasts and correlated with transcription cycles. Results indicate that cycles of DNA methylation (zeige HELLS Antikörper) contribute to the regulation of BMAL1 rhythms in the brain.
TFEB (zeige TFEB Antikörper) regulates PER3 expression via glucose-dependent effects on CLOCK/BMAL1
found that overexpression of both Clock and Bmal1 suppressed cell growth
the second half of the photolyase homology region (PHR) of CRY (zeige CRY2 Antikörper) is important for repression through facilitating interaction with BMAL1
Results indicated that pBMAL1 cDNA had a coding region of 1,878 bp and shared 94.36, 89.85 and 89.79% identity with human, mouse and rat BMAL1. pBMAL1 expression levels in different tissues were studied.
The Smad3 (zeige SMAD3 Antikörper) and Bmal1 regulate p21 (zeige D4S234E Antikörper) and S100A4 (zeige S100A4 Antikörper) expression in myocardial stromal fibroblasts through TNF-alpha (zeige TNF Antikörper).
Data demonstrated that the circadian rhythm of testosterone synthesis in TM3 (zeige TPM1 Antikörper) cells was disturbed following Fen treatment as evidenced by changes in the circadian rhythmicity of core clock genes (Bmal1, Rev-erbalpha (zeige NR1D1 Antikörper), Roralpha).
The circadian clock component Bmal1 is involved in blood brain barrier homeostasis.
Study shows a role for Bmal1, the endogenous circadian clock, in glucose metabolism in the skeletal muscle. Findings implicate altered molecular clock dictating significant changes in altered substrate metabolism in the absence of feeding or activity changes.
A significant proportion of circadian lncRNAs are expressed at enhancer regions, mostly bound by two key circadian transcription factors, BMAL1 and REV-ERBalpha (zeige NR1D1 Antikörper).
A cis (zeige CISH Antikörper)/trans isomerization switch in the BMAL1 transactivation domain controls circadian rhythms. Conformationally locking the switch or inhibiting prolyl isomerases influences circadian period to suggest that slow protein dynamics play a role in timekeeping.
Bmal1 deficiency in macrophages promotes atherosclerosis by enhancing recruitment of Ly6chi monocytes to atherosclerotic lesions.
Bmal1 autophagic degradation and Bmal1 role in glucose homeostasis
These results suggest that miR (zeige MLXIP Antikörper)-27b-3p plays an important role in the posttranscriptional regulation of BMAL1 protein in the liver.
The protein encoded by this gene is a basic helix-loop-helix protein that forms a heterodimer with CLOCK. This complex binds an E-box upstream of the PER1 gene, activating this gene and possibly other circadian rhythym-associated genes. Three transcript variants encoding two different isoforms have been found for this gene.
ARNT-like protein 1, brain and muscle
, PAS domain-containing protein 3
, aryl hydrocarbon receptor nuclear translocator-like protein 1
, bHLH-PAS protein JAP3
, basic-helix-loop-helix-PAS orphan MOP3
, basic-helix-loop-helix-PAS protein MOP3
, brain and muscle ARNT-like 1
, class E basic helix-loop-helix protein 5
, member of PAS protein 3
, member of PAS superfamily 3
, brain and muscle ARNT-like protein 1
, bHLH-PAS transcription factor BMAL1
, clock protein
, aryl hydrocarbon receptor nuclear translocator-like
, Brain and muscle ARNT-like 1
, aryl hydrocarbon receptor nuclear translocator-like protein 1-like
, brain and muscle Arnt-like protein 1
, bHLH-PAS transcription factor