C-JUN Proteine (JUN)

Jun Proto-Oncogene Proteine (JUN)
Auf www.antikoerper-online.de finden Sie aktuell 24 Jun Proto-Oncogene (JUN) Proteine von 10 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen C-JUN Antikörper (876) und C-JUN Kits (102) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 1063 C-JUN Produkte verfügbar.
AP-1, AP1, B230310J22Rik, Bsk, BSK/DJNK, c-jun, CG2275, CG5680, cJun, D-JNK, d-JRA, d-jun, D-jun/Jra, D-junk, dAP-1, DBSK/JNK, dJNK, DJNK/bsk, dJra, djun, dm-Jun, Dmel\\CG2275, Dmel\\CG5680, fj36h07, jnk, JNK/SAPK, jra, jun, Junc, Junk, l(2)46Ef, l(2)IA109, l(2R)IA109, p39, SAPKa, V, wu:fj36h07, zgc:65863
alle Proteine anzeigen Gen GeneID UniProt
JUN 12570 O35926
JUN 3725 P05412
JUN 24516 P17325

Weitere Synonyme anzeigen

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Am meisten referenzierte C-JUN Proteine

  1. Human C-JUN Protein expressed in Escherichia coli (E. coli) - ABIN667382 : Bannister, Gottlieb, Kouzarides, Jackson: c-Jun is phosphorylated by the DNA-dependent protein kinase in vitro; definition of the minimal kinase recognition motif. in Nucleic acids research 1993 (PubMed)
    Zeige alle 2 Referenzen für 667382

  2. Human C-JUN Protein expressed in Escherichia coli (E. coli) - ABIN411906 : Michaelis, Ansar, Chen, Reiff, Seyb, Himes, Audus, Georg: {beta}-Amyloid-induced neurodegeneration and protection by structurally diverse microtubule-stabilizing agents. in The Journal of pharmacology and experimental therapeutics 2005 (PubMed)

Weitere Proteine zu C-JUN Interaktionspartnern

Xenopus laevis Jun Proto-Oncogene (JUN) Interaktionspartner

  1. AP-1(c-Jun/FosB (zeige FOSB Proteine)) may play a role in neurogenesis via the induction of FoxD5b expression during early vertebrate development

  2. The cJun transcription factor bound to a variant cAMP response element in the promoter region of tlx3 (zeige TLX3 Proteine) and modulated transcription and regulated neurotransmitter phenotype via its transactivation domain

Fruit Fly (Drosophila melanogaster) Jun Proto-Oncogene (JUN) Interaktionspartner

  1. Mir (zeige MYLIP Proteine)-8 modulates Drosophila C virus replication by negative regulation of dJun.

  2. Here we uncover a cell non-autonomous requirement for the Epidermal growth factor receptor (Egfr (zeige EGFR Proteine)) pathway in the lateral epidermis for sustained dpp (zeige TGFb Proteine) expression in the LE. Specifically, we demonstrate that Egfr (zeige EGFR Proteine) pathway activity in the lateral epidermis prevents expression of the gene scarface (scaf), encoding a secreted antagonist of JNK (zeige MAPK8 Proteine) signaling

  3. Tau and spectraplakin promote synapse formation and maintenance through Jun kinase (zeige MAPK9 Proteine) and neuronal trafficking.

  4. n addition to significantly increasing the number of JNK (zeige MAPK8 Proteine) target genes identified so far, our results reveal that the LE is a highly heterogeneous morphogenetic organizer, sculpted through crosstalk between JNK (zeige MAPK8 Proteine), segmental and AP signalling. This fine-tuning regulatory mechanism is essential to coordinate morphogenesis and dynamics of tissue sealing

  5. malignant transformation of the ras(V12)scrib(1) tumors requires bZIP protein Fos, the ETS (zeige ETS1 Proteine)-domain factor Ets21c and the nuclear receptor Ftz-F1 (zeige NR5A2 Proteine), all acting downstream of Jun-N-terminal kinase (zeige MAPK8 Proteine).

  6. Diminished MTORC1-dependent JNK (zeige MAPK8 Proteine) activation underlies the neurodevelopmental defects associated with lysosomal dysfunction.

  7. ROS (zeige ROS1 Proteine)/JNK (zeige MAPK8 Proteine)/p38 (zeige MAPK14 Proteine)/Upd (zeige UROD Proteine) stress responsive module restores tissue homeostasis. This module is not only activated after cell death induction but also after physical damage and reveals one of the earliest responses for imaginal disc regeneration.

  8. Significantly, the JNK (zeige MAPK8 Proteine) pathway is responsible for the majority of the phenotypes and transcriptional changes downstream of Notch (zeige NOTCH1 Proteine)-Src (zeige SRC Proteine) synergy.

  9. This study demonstrated that the mechanism by which Bsk (zeige FRK Proteine) is required for pruning is through reducing the membrane levels of the adhesion molecule (zeige NCAM1 Proteine) Fasciclin II (zeige NCAM2 Proteine) (FasII)

  10. Jra recruits the HP1a (zeige CBX5 Proteine)/KDM4A (zeige KDM4A Proteine) complex to its gene body region upon osmotic stress to reduce H3K36 methylation levels and disrupt H3K36 methylation-dependent histone deacetylation

Pig (Porcine) Jun Proto-Oncogene (JUN) Interaktionspartner

  1. Porcine reproductive and respiratory syndrome virus -activated TAK-1 (zeige NR2C2 Proteine) was essential for the activation of JNK (zeige MAPK8 Proteine) and NF-kappaB (zeige NFKB1 Proteine) pathways and IL-8 (zeige IL8 Proteine) expression.

  2. The effects of prostaglandin F2alpha administration on transcription factor AP-1 expression and the expression of downstream genes involved in luteolysis are reported.

Rabbit Jun Proto-Oncogene (JUN) Interaktionspartner

  1. ICAM1 (zeige ICAM1 Proteine) and IL10 (zeige IL10 Proteine) were upregulated in ventilator-induced lung injury. Nuclear transcription factor AP-1 may be responsible for this upregulation.

Mouse (Murine) Jun Proto-Oncogene (JUN) Interaktionspartner

  1. AP1 factors are important regulators of adult taste cell renewal and their downregulation negatively impacts taste maintenance.

  2. these data indicate that MEF2 (zeige MEF2C Proteine) and AP-1 confer antagonistic regulation of Hspb7 (zeige HSPB7 Proteine) gene expression in skeletal muscle, with implications for autophagy and muscle atrophy.

  3. results suggest that fibroblasts, c-Jun, and IGF-1 (zeige IGF1 Proteine) play key roles in mediating stromal-epithelial interactions that are required for the therapeutic effects of finasteride in benign prostate epithelial cells

  4. These findings highlight a key role of the TLR4 (zeige TLR4 Proteine)-NOS1 (zeige NOS1 Proteine)-AP1 signaling axis in regulating macrophage polarization

  5. Data suggest that Sf1 and c-jun interact and cooperate to activate the Fdx1 promoter in MA-10 (tumorigenic cell line) and TM3 (non-tumorigenic cell line) Leydig cells; such activation requires different regulatory elements located between -124 and -306 bp of Fdx1 promoter and involves recruitment of Sf1 to this region. (Sf1 = splicing factor 1; c-jun = proto-oncogene c-jun; Fdx1 = ferredoxin 1)

  6. In this study, we discovered that selective upregulation of p39 (zeige ATP6V0D1 Proteine) is the underlying mechanism that accommodates the increased functional requirement of Cdk5 (zeige CDK5 Proteine) activation during neuronal differentiation. In addition, we demonstrated that p39 (zeige ATP6V0D1 Proteine) selectively directs Cdk5 (zeige CDK5 Proteine) to phosphorylate protein substrates essential for axonal development, dendritic spine formation, and synaptogenesis. Moreover, our studies suggest opposing roles o

  7. NF-kappaB (zeige NFKB1 Proteine) and c-Jun coregulate lipopolysaccharide-induced Fra-1 (zeige FOSL1 Proteine) transcription.

  8. BATF/JUN-B and BATF/C-JUN complexes play important roles in OA cartilage destruction through regulating anabolic and catabolic gene expression in chondrocytes.

  9. this study shows that c-Jun regulates the activation state of macrophages and promotes arthritis via differentially regulating cyclooxygenase-2 (zeige PTGS2 Proteine) and arginase-1 (zeige ARG1 Proteine) levels

  10. PLIO treatment inhibited nuclear factorkappaB (NFkappaB) nuclear translocation in B16F10 cells. In addition, PLIO treatment inhibited the phosphorylation of c-Jun Nterminal kinases and AKT (zeige AKT1 Proteine)

Human Jun Proto-Oncogene (JUN) Interaktionspartner

  1. Our results indicate that assessing AP1 (zeige FOSB Proteine) and PEA3 (zeige ETV4 Proteine) transcription factor status might be a good indicator of OAC status. However, we could not detect any associations with disease stage or patient treatment regime. This suggests that the PEA3 (zeige ETV4 Proteine)-AP1 (zeige FOSB Proteine) regulatory module more likely contributes more generally to the cancer phenotype. In keeping with this observation, depletion of ETV1 (zeige ETV1 Proteine) and/or ETV4 (zeige ETV4 Proteine) causes an OAC cell growth defect

  2. shRNA-mediated inhibition of JUN decreases AML (zeige RUNX1 Proteine) cell survival and propagation in vivo. These data uncover a previously unrecognized role of JUN as a regulator of the unfolded protein response

  3. These findings demonstrate an essential role for the ERK pathway together with c-JUN and c-FOS in the differentiation activity of LukS-PV.

  4. The present study defines the minimal TIM-3 (zeige HAVCR2 Proteine) promoter region and demonstrates its interaction with c-Jun during TIM-3 (zeige HAVCR2 Proteine) transcription in CD4 (zeige CD4 Proteine)(+) T cells.

  5. Taken together, our data demonstrate that JNK (zeige MAPK8 Proteine) regulates triple-negative breast cancer (TNBC)tumorigenesis by promoting CSC phenotype through Notch1 (zeige NOTCH1 Proteine) signaling via activation of c-Jun and indicate that JNK/c-Jun/Notch1 (zeige NOTCH1 Proteine) signaling is a potential therapeutic target for TNBC

  6. Regulation of osteosarcoma cell lung metastasis by the c-Fos/AP-1 target FGFR1

  7. c-jun promoted FOXK1-mediated proliferation and metastasis via orthotopic implantation.

  8. Data provide evidence that AP-1 (zeige FOSB Proteine) is a key determinant of endocrine resistance of breast cancer cells by mediating a global shift in the estrogen receptor (zeige ESR1 Proteine) transcriptional program.

  9. Comparison of how AP-1 (Jun/Jun dimer) and Epstein-Barr virus Zta recognize methyl groups within their cognate response elements

  10. this study revealed the functional and mechanistic links between CDK5 (zeige CDK5 Proteine) and the oncogenic ERK5 (zeige MAPK7 Proteine)-AP-1 (zeige FOSB Proteine) signaling pathway in the pathogenesis of colorectal cancer.

Zebrafish Jun Proto-Oncogene (JUN) Interaktionspartner

  1. These results support a role for trim69 (zeige TRIM69 Proteine) in the development of the zebrafish brain through ap-1 pathway.

  2. CPEB-1 (zeige CPEB1 Proteine) control of c-Jun mRNA translation regulates GH gene expression and resulting downstream signaling events (e.g., synaptic plasticity) in the mouse hippocampus.

Cow (Bovine) Jun Proto-Oncogene (JUN) Interaktionspartner

  1. The present data indicate that bovine dialyzable leukocyte extract can block the AP-1 DNA-binding activity and expression of several transcriptions factors in breast cancer cells.

  2. dynamic compression stimulates cell proliferation and proteoglycan (zeige Vcan Proteine) synthesis in the presence of IL-1beta (zeige IL1B Proteine) and/or inhibitors of the MAPKs and NFkappaB and AP-1 signalling pathways

C-JUN (JUN) Protein Überblick

Protein Überblick

This gene is the putative transforming gene of avian sarcoma virus 17. It encodes a protein which is highly similar to the viral protein, and which interacts directly with specific target DNA sequences to regulate gene expression. This gene is intronless and is mapped to 1p32-p31, a chromosomal region involved in both translocations and deletions in human malignancies.

Alternative names and synonyms associated with C-JUN (JUN)

  • jun oncogene (jun)
  • basket (bsk)
  • C-JUN protein (C-JUN)
  • c-Jun protein (C-JUN)
  • c-jun transcription factor (C-JUN)
  • cyclin-dependent kinase 5, regulatory subunit 2 (p39) (Cdk5r2)
  • Jun oncogene (Jun)
  • jun proto-oncogene (JUN)
  • jun proto-oncogene (jun)
  • jun proto-oncogene (Jun)
  • Jun-related antigen (Jra)
  • AP-1 Protein
  • AP1 Protein
  • B230310J22Rik Protein
  • Bsk Protein
  • BSK/DJNK Protein
  • c-jun Protein
  • CG2275 Protein
  • CG5680 Protein
  • cJun Protein
  • D-JNK Protein
  • d-JRA Protein
  • d-jun Protein
  • D-jun/Jra Protein
  • D-junk Protein
  • dAP-1 Protein
  • DBSK/JNK Protein
  • dJNK Protein
  • DJNK/bsk Protein
  • dJra Protein
  • djun Protein
  • dm-Jun Protein
  • Dmel\\CG2275 Protein
  • Dmel\\CG5680 Protein
  • fj36h07 Protein
  • jnk Protein
  • JNK/SAPK Protein
  • jra Protein
  • jun Protein
  • Junc Protein
  • Junk Protein
  • l(2)46Ef Protein
  • l(2)IA109 Protein
  • l(2R)IA109 Protein
  • p39 Protein
  • SAPKa Protein
  • V Protein
  • wu:fj36h07 Protein
  • zgc:65863 Protein

Bezeichner auf Proteinebene für Jun Proto-Oncogene Proteine (JUN)

v-jun sarcoma virus 17 oncogene homolog , CG5680-PB , CG5680-PE , CG5680-PF , JNK , JUN kinase , Jun N-terminal kinase , Jun NH2-terminal kinase , Jun-N-terminal kinase , Jun-kinase , bsk-PB , bsk-PE , bsk-PF , c-Jun N-terminal kinase , c-Jun aminoterminal kinase , c-Jun-N-terminal kinase , drosophila JNK , AP1 , V-jun avian sarcoma virus 17 oncogene homolog , activator protein 1 , proto-oncogene c-jun , transcription factor AP-1 , CDK5 activator 2 , cyclin-dependent kinase 5 activator 2 , cyclin-dependent kinase 5 regulatory subunit 2 , p39I , AH119 , immediate early , jun A , Jun activation domain binding protein , enhancer-binding protein AP1 , jun oncogene , p39 , proto-oncogene c-Jun , v-jun avian sarcoma virus 17 oncogene homolog , Avian sarcoma virus 17 (v-jun) oncogene homolog , Jun oncogene , v-jun sarcoma virus 17 oncogene , CG2275-PA , CG2275-PB , CG2275-PC , Jra-PA , Jra-PB , Jra-PC , Jun related antigen , complementation group V , lethal(2)1A109 , lethal(2)IA109

379050 Xenopus laevis
44801 Drosophila melanogaster
396913 Sus scrofa
443219 Ovis aries
100008856 Oryctolagus cuniculus
12570 Mus musculus
16476 Mus musculus
3725 Homo sapiens
335916 Danio rerio
24516 Rattus norvegicus
399400 Xenopus laevis
424673 Gallus gallus
609429 Canis lupus familiaris
280831 Bos taurus
100170668 Ovis aries
36057 Drosophila melanogaster
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