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Exposure to blue light is required for an in vivo-association of CRY1 (Montrer CRY1 Kits ELISA) and CRY2 with COP1.
Data show that the effect of 3-bromo-7-nitroindazole (3B7N) treatment on gene expression in cryptochromes cry1cry2 is considerably smaller than that in the wild type, indicating that 3B7N specifically interrupts cryptochrome function in the control of seedling development in a light-dependent manner.
It describes minimal functional CRY2 and CIB1 (Montrer CIB1 Kits ELISA) domains maintaining light-dependent interaction and new signaling mutations affecting Arabidopsis thaliana cryptochrome 2 (AtCRY2) photocycle kinetics.
this study identified BIC1 (blue-light inhibitor of cryptochromes 1) as an inhibitor of plant cryptochromes that binds to CRY2 to suppress the blue light-dependent dimerization, photobody formation, phosphorylation, degradation, and physiological activities of CRY2.
the blue light-dependent CRY2 degradation is significantly impaired in the temperature-sensitive cul1 (Montrer CUL1 Kits ELISA) mutant allele (axr6 (Montrer CUL1 Kits ELISA)-3), especially under the non-permissive temperature.
For growth under a canopy, where blue light is diminished, CRY1 and CRY2 perceive this change and respond by directly contacting two bHLH transcription factors, PIF4 and PIF5.
Arabidopsis thaliana cry2 proteins containing Trp (Montrer TBPL1 Kits ELISA) triad mutations indeed undergo robust photoreduction in living cultured insect cells.
data showed that mutations in the serine residues within and outside the serine cluster diminished blue light-dependent CRY2 phosphorylation, degradation, and physiological activities.
Our study demonstrates that CIBs function redundantly in regulating CRY2-dependent flowering, and that different CIBs form heterodimers to interact with the non-canonical E-box DNA in vivo.
Studies show that CK1.3 (At4g28880) and CK1.4 (At4g28860) directly phosphorylate CRY2 at Ser (Montrer SIGLEC1 Kits ELISA)-587 and Thr (Montrer TRH Kits ELISA)-603 in vitro and negatively regulate CRY2 stability, which are stimulated by blue light.
The FOXM1 (Montrer FOXM1 Kits ELISA) is a negative regulator of CRY2 in breast cancer via enhancing methylation in CRY2 promoter and its high expression is an independent predictor of favorable MR-free survival in ER+ breast cancer patients.
CRY2 and FBXL3 (Montrer FBXL3 Kits ELISA) cooperatively degrade c-MYC (Montrer MYC Kits ELISA) preventing the development of cancer.
The present study identified USP7 (Montrer USP7 Kits ELISA) and TDP-43 (Montrer TARDBP Kits ELISA) as the regulators of CRY1 (Montrer CRY1 Kits ELISA) and CRY2, underscoring the significance of the stability control process of CRY proteins for period determination in the mammalian circadian clockwork.
For the first time, we show that Cry 2 rs2292910 and MTNR1B (Montrer MTNR1B Kits ELISA) rs3781638 are associated with osteoporosis in a Chinese geriatric cohort.
Altered CRY1 (Montrer CRY1 Kits ELISA) and CRY2 expression patterns and the interplay with the genetic landscape in colon cancer cells may underlie phenotypic divergence.
Given the distinct characteristics of the C-terminal tails of the CRY1 (Montrer CRY1 Kits ELISA) and CRY2 proteins, our study addresses a long-standing hypothesis that the ratio of these two CRY molecules affects the clock period.
data may point to CRY2 as a novel switch in hepatic fuel metabolism promoting triglyceride storage and, concomitantly, limiting glucose production
Data indicate that cryptochrome 2 (CRY2) knockdown leads to chemosensitivity of colorectal cancer cell lines.
CRY2 and REV-ERB ALPHA (Montrer NR1D1 Kits ELISA) as the clock genes upregulated in obesity during the 24 h period and that REV-ERB ALPHA (Montrer NR1D1 Kits ELISA) is an important gene associated with MS.
these observations suggest a biologically plausible season-dependent association between SNPs at CRY1 (Montrer CRY1 Kits ELISA), CRY2 and MTNR1B (Montrer MTNR1B Kits ELISA) and glucose homeostasis.
In vivo knockdown of Rfk (Montrer RFK Kits ELISA), Riboflavin (vitamin B2) kinase essential for FAD (Montrer FANCD2 Kits ELISA) synthesis, altered the expression rhythms of CRY1 (Montrer CRY1 Kits ELISA), CRY2, and PER1 (Montrer PER1 Kits ELISA)
Data show that cryptochrome Cry1 (Montrer CRY1 Kits ELISA) and Cry2 expression must be circadian and appropriately phased to support rhythms, and arginine vasopressin (AVP (Montrer AVP Kits ELISA)) receptor signaling is required to impose circuit-level circadian function.
Data suggest that cryptochromes (Cry1 (Montrer CRY1 Kits ELISA) and Cry2) mediate periodic binding of Ck2b (Montrer CSNK2B Kits ELISA) (casein kinase 2beta) to Bmal1 (aryl hydrocarbon receptor nuclear translocator-like (Montrer ARNTL Kits ELISA) protein) and thus inhibit Bmal1 (Montrer ARNTL Kits ELISA)-Ser90 phosphorylation by Ck2a (Montrer CSNK2A1 Kits ELISA) (casein kinase 2alpha).
Cry2 exerts a critical role in the control of depression-related emotional states and modulates the chronobiological gene expression profile in the mouse amygdala.
Cry1/Cry2-deficient mice had significantly lower N6- methyladenosine methylation of RNA and lost the circadian rhythm of N6-methyladenosine levels in RNA.
Data show that the intermolecular zinc finger is important for period circadian protein (PER2 (Montrer PER2 Kits ELISA))-cryptochrome 2 (CRY2) complex formation.
Report compression of daily activity time in Cry2 mutant mice.
Data show that Ser557 phosphorylation of CRY2 promotes CRY2 degradation and inhibits the overaccumulation of the CRY2-PER2 (Montrer PER2 Kits ELISA) complex in the nucleus.
member of a family of blue-light photoreceptors\; may regulate circadian rhythm
, cryptochrome 2
, cryptochrome Cry2
, cryptochrome 2 (photolyase-like)
, growth-inhibiting protein 37