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抗Human MAPK9 抗体:
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抗Rat (Rattus) MAPK9 抗体:
Human Polyclonal MAPK9 Primary Antibody for IHC (p), WB - ABIN1882172
Gupta, Barrett, Whitmarsh, Cavanagh, Sluss, Dérijard, Davis: Selective interaction of JNK protein kinase isoforms with transcription factors. in The EMBO journal 1996
Show all 4 Pubmed References
Human Polyclonal MAPK9 Primary Antibody for ELISA, WB - ABIN4327970
Leppä, Bohmann: Diverse functions of JNK signaling and c-Jun in stress response and apoptosis. in Oncogene 1999
The MAP kinase (显示 MAPK1 抗体) JNK2 mediates cigarette smoke-induced tissue factor (显示 F3 抗体) activation, arterial thrombosis and reactive oxygen species production.
We found p-JNK2 up-regulation in AUC and its early down-regulation in UC-CRC (显示 CALR 抗体) and CRC (显示 CALR 抗体) carcinogenesis.
JNK2 was a novel direct target of miR (显示 MLXIP 抗体)-20a-5p.
The release of infectious respiratory syncytial virus (RSV) virions from infected cells was significantly reduced by JNK1 (显示 MAPK8 抗体)/2 siRNA knockdown, implicating JNK1 (显示 MAPK8 抗体)/2 as a key host factor for RSV virus production.
PXR (显示 NR1I2 抗体) regulates the intestinal epithelial barrier during inflammation by modulating cytokine-induced MLCK (显示 MYLK 抗体) expression and JNK1 (显示 MAPK8 抗体)/2 activation
Phloretin is able to inhibit NSCLC A549 cell growth by inducing apoptosis through P38 MAPK (显示 MAPK14 抗体) and JNK1 (显示 MAPK8 抗体)/2 pathways, and therefore may prove to be an adjuvant to the treatment of non-small cell lung cancer
In hepatocytes, JNK1 (显示 MAPK8 抗体) and JNK2 appear to have combined effects in protecting from drug-induced liver injury.
Inhibition of JNK1 (显示 MAPK8 抗体)/2 activity suppressed Hedgehog (显示 SHH 抗体) pathway activity in acquired chemoresistant cancer cells.
although JNK (显示 MAPK8 抗体) activation and RIP3 (显示 RIPK3 抗体) expression are induced by FS, neither contributes to the liver injury.
These data suggest that JNK1 (显示 MAPK8 抗体)/2 may play an important role in promoting the replication of Penicillium marneffei.
activation of JNK (显示 MAPK8 抗体) in the endoplasmic reticulum stress response precedes activation of XBP1 (显示 XBP1 抗体).
JNK-2 regulates aggrecan (显示 ACAN 抗体) degradation in cultured murine cartilage and surgically induced osteoarthritis in vivo following mechanical destabilization of the knee joint.
activation of astrocyte MMP2 (显示 MMP2 抗体)/JNK1 (显示 MAPK8 抗体)/2 contributes to the pathogenesis of pain hypersensitivity in the complex regional pain syndrome model
JNK1 (显示 MAPK8 抗体)/2-dependent regulation of p66ShcS36 phosphorylation, is reported.
This study demonstrated that the disruption of JNK2 appears to have a greater impact on tolerance than the other isoforms in the tail-flick but not the hot-plate test.
although JNK (显示 MAPK8 抗体) activation and RIP3 (显示 MPRIP 抗体) expression are induced by FS, neither contributes to the liver injury.
morphine activated JNK2 through an arrestin-independent Src- and PKC-dependent mechanism, whereas fentanyl activated JNK2 through a Src-GRK3/arrestin-2-dependent and PKC-independent mechanism.
studies herein support that JNK2 inhibits cell differentiation in normal and cancer-derived mammary cells
this study indicates that JNK2 is a physiological kinase responsible for eNOS (显示 NOS3 抗体)-Ser (显示 SIGLEC1 抗体)(116) phosphorylation and regulates NO production.
Data show that proinflammatory cytokines induction was ERK1/2 and JNK1 (显示 MAPK8 抗体)/2 dependent.
These data suggest that the p38 (显示 MAPK14 抗体) and JNK (显示 MAPK8 抗体) signaling pathways play pivotal roles in PRRSV replication and may regulate immune responses during virus infection.
MPK9 and MPK12 (显示 MAPK12 抗体) are positive regulators of salicylic acid signaling in Arabidopsis guard cells.
MPK9 and MPK12 (显示 MAPK12 抗体) are key regulators mediating both abscisic acid (ABA) and Methyl jasmonate (MeJA) signalling in guard cells.
Data suggest that MPK9 is autoactivated via phosphorylation independent of any upstream MAPK (显示 MAPK1 抗体) kinase signaling; autophosphorylation occurs at both threonine and tyrosine residues in Thr (显示 TRH 抗体)-Asp (显示 ASIP 抗体)-Tyr (显示 TYR 抗体) motif and in C-terminal regulatory extension.
MPK9 and MPK12 (显示 MAPK12 抗体) function redundantly downstream of extracellular reactive oxygen production and intracellular accumulation, cytosolic alkalisation and Ca(2 (显示 CA2 抗体)+)cytosolic oscillation in yeast elcictor-induced stomatal closure
MPK9 and MPK12 (显示 MAPK12 抗体) act downstream of ROS (显示 ROS1 抗体) and cytosolic Ca2 (显示 CA2 抗体)+ and upstream of anion channels in the guard cell abscisic acid signaling cascade.
MAP kinases MPK9 and MPK12 (显示 MAPK12 抗体) are preferentially expressed in guard cells and positively regulate ROS (显示 ROS1 抗体)-mediated ABA signaling.
The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase targets specific transcription factors, and thus mediates immediate-early gene expression in response to various cell stimuli. It is most closely related to MAPK8, both of which are involved in UV radiation induced apoptosis, thought to be related to the cytochrome c-mediated cell death pathway. This gene and MAPK8 are also known as c-Jun N-terminal kinases. This kinase blocks the ubiquitination of tumor suppressor p53, and thus it increases the stability of p53 in nonstressed cells. Studies of this gene's mouse counterpart suggest a key role in T-cell differentiation. Several alternatively spliced transcript variants encoding distinct isoforms have been reported.
mitogen-activated protein kinase 9
, Jun kinase
, MAP kinase 9
, MAPK 9
, c-Jun N-terminal kinase 2
, c-Jun kinase 2
, stress-activated protein kinase 1a
, stress-activated protein kinase JNK2
, JNK/SAPK alpha
, mitogen activated protein kinase 9
, protein kinase, mitogen-activated 9
, stress activated protein kinase alpha II
, janus kinase 2
, c-JUN amino-terminal kinase-2 alpha1