You are viewing an incomplete version of our website. Please click to reload the website as full version.

Browse our C-JUN Proteins (JUN)

Full name:
Jun Proto-Oncogene Proteins (JUN)
On www.antibodies-online.com are 23 Jun Proto-Oncogene (JUN) Proteins from 10 different suppliers available. Additionally we are shipping C-JUN Antibodies (836) and C-JUN Kits (99) and many more products for this protein. A total of 1019 C-JUN products are currently listed.
Synonyms:
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
list all proteins Gene Name GeneID UniProt
JUN 12570 O35926
JUN 3725 P05412
JUN 24516 P17325

Show all synonyms

C-JUN Proteins (JUN) by Origin

Select your origin of interest

Top referenced C-JUN Proteins

  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)
    Show all 2 references for ABIN667382

  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)

More Proteins for C-JUN Interaction Partners

Xenopus laevis Jun Proto-Oncogene (JUN) interaction partners

  1. AP-1(c-Jun/FosB (show FOSB Proteins)) 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 (show TLX3 Proteins) and modulated transcription and regulated neurotransmitter phenotype via its transactivation domain

Fruit Fly (Drosophila melanogaster) Jun Proto-Oncogene (JUN) interaction partners

  1. Tau and spectraplakin promote synapse formation and maintenance through Jun kinase (show MAPK9 Proteins) and neuronal trafficking.

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

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

  4. Diminished MTORC1-dependent JNK (show MAPK8 Proteins) activation underlies the neurodevelopmental defects associated with lysosomal dysfunction.

  5. ROS (show ROS1 Proteins)/JNK (show MAPK8 Proteins)/p38 (show MAPK14 Proteins)/Upd (show UROD Proteins) 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.

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

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

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

  9. Study solves the crystal structure of unphosphorylated DJNK in complex with adenylyl imidodiphosphate (AMP (show AMPH Proteins)-PNP (show NP Proteins)) and magnesium.

  10. PERK/ATF4 activated the JNK pathway through Rac1 and Slpr activation in apoptotic cells.

Pig (Porcine) Jun Proto-Oncogene (JUN) interaction partners

  1. 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) interaction partners

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

Mouse (Murine) Jun Proto-Oncogene (JUN) interaction partners

  1. NF-kappaB (show NFKB1 Proteins) and c-Jun coregulate lipopolysaccharide-induced Fra-1 (show FOSL1 Proteins) transcription.

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

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

  4. 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 (show AKT1 Proteins)

  5. Anxa5 (show ANXA5 Proteins) mediates the in vitro malignant behaviours of murine hepatocarcinoma Hca-F cells via ERK2 (show MAPK1 Proteins)/c-Jun/p-c-Jun(Ser73) and ERK2 (show MAPK1 Proteins)/E-cadherin (show CDH1 Proteins) pathways.

  6. These findings indicate that c-Jun has important functions during HBV-associated tumorigenesis by promoting hepatocyte proliferation as well as progression of dysplasia

  7. The TLR4 (show TLR4 Proteins) pathway may play an important role in regulating AP-1 activation

  8. These observations suggest that the antiinflammatory properties of crebanine may stem from the inhibition of proinflammatory mediators via suppression of the NF-kappaB (show NFKB1 Proteins), AP-1, MAPKs, and Akt (show AKT1 Proteins) signaling pathways.

  9. In a model of heavy metal poisoning, copper contamination of drinking water (as can occur with corrosion in aging plumbing systems) up-regulates binding of transcription factor AP-1 in neurons of brain, even in low concentrations.

  10. Transplant-induced reactivation of murine cytomegalovirus immediate early gene expression is associated with recruitment of NF-kappaB (show NFKB1 Proteins) and AP-1 to the major immediate early promoter.

Human Jun Proto-Oncogene (JUN) interaction partners

  1. The authors find that PRR7 inhibits the ubiquitination of c-Jun by E3 ligase SCF (show KITLG Proteins)(FBW) (7) (FBW7 (show FBXW7 Proteins)), increases c-Jun-dependent transcriptional activity, and promotes neuronal death.

  2. melatonin synergistically augmented the sorafenib-induced apoptosis after 48 hours incubation, which was in accordance with the activation of caspase-3 (show CASP3 Proteins) and the JNK/c-jun pathway.

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

  4. the current studies provide evidence showing that c-Jun directly binds to a consensus binding sequence within the GNA12-5' regulatory region, thereby regulating GNA12 transcription.

  5. we demonstrated that miR (show MLXIP Proteins)-22 promoted monocyte/macrophage differentiation, and MECOM (EVI1 (show MECOM Proteins)) mRNA is a direct target of miR (show MLXIP Proteins)-22 and MECOM (EVI1 (show MECOM Proteins)) functions as a negative regulator in the differentiation.The miR (show MLXIP Proteins)-22-mediated MECOM (show MECOM Proteins) degradation increased c-Jun but decreased GATA2 (show GATA2 Proteins) expression, which results in increased interaction between c-Jun and PU.1

  6. Gene expression profiling and pathway analysis followed by pharmacological screening identified activated ERK (show EPHB2 Proteins) and JNK (show MAPK8 Proteins) signaling as key drivers of neurodegeneration in mutant SOD1 (show SOD1 Proteins) motor neurons. Genetic correction of SOD1 (show SOD1 Proteins) mutant iPSCs Reveals ERK (show EPHB2 Proteins) and JNK (show MAPK8 Proteins) Activated AP1 (show FOSB Proteins) as a Driver of Neurodegeneration in Amyotrophic Lateral Sclerosis.

  7. the absence of 14-3-3sigma leads to the nuclear accumulation and stabilization of c-Jun, suggesting that 14-3-3sigma regulates the subcellular localization of c-Jun.

  8. Suggest UCA1 and C-JUN mRNA as promising diagnostic and prognostic markers in hepatocellular carcinoma.

  9. During inflammatory conditions, AP-1 (show FOSB Proteins) and Sp1 (show PSG1 Proteins) sustained the expression of ADAMTS7 (show ADAMTS7 Proteins), and ADAMTS7 (show ADAMTS7 Proteins) sustained the expression of catabolic genes in nucleus pulposus cells

  10. our data strongly suggest that AQCA-mediated suppression of inflammatory responses could be managed by a direct interference of signaling cascades including IRAK (show IRAK1 Proteins) and Syk (show SYK Proteins), linked to the activation of NF-kappaB (show NFKB1 Proteins) and AP-1 (show FOSB Proteins).

Zebrafish Jun Proto-Oncogene (JUN) interaction partners

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

  2. CPEB-1 (show CPEB1 Proteins) 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) interaction partners

  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 (show Vcan Proteins) synthesis in the presence of IL-1beta (show IL1B Proteins) and/or inhibitors of the MAPKs and NFkappaB and AP-1 signalling pathways

C-JUN (JUN) Protein Profile

Protein Summary

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

Protein level used designations for Jun Proto-Oncogene Proteins (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

GENE ID SPECIES
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
Selected quality suppliers for C-JUN Proteins (JUN)
Did you look for something else?