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anti-Human PAK1 Antikörper:
anti-Mouse (Murine) PAK1 Antikörper:
anti-Rat (Rattus) PAK1 Antikörper:
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Human Polyclonal PAK1 Primary Antibody für IHC - ABIN966797
Alexander, Yang, Hinds: Cellular senescence requires CDK5 repression of Rac1 activity. in Molecular and cellular biology 2004
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Human PAK1 Primary Antibody für IHC - ABIN966796
Thiel, Reeder, Pfaff, Coleman, Sells, Chernoff: Cell cycle-regulated phosphorylation of p21-activated kinase 1. in Current biology : CB 2002
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Human Polyclonal PAK1 Primary Antibody für WB - ABIN1944750
Brown, Stowers, Baer, Trejo, Coughlin, Chant: Human Ste20 homologue hPAK1 links GTPases to the JNK MAP kinase pathway. in Current biology : CB 1997
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Human Polyclonal PAK1 Primary Antibody für DB, IF - ABIN389799
El-Baba, Mahadevan, Fahlbusch, S, Rau, Gali-Muhtasib, Schneider-Stock: Thymoquinone-induced conformational changes of PAK1 interrupt prosurvival MEK-ERK signaling in colorectal cancer. in Molecular cancer 2014
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Human Monoclonal PAK1 Primary Antibody für IF, IHC (p) - ABIN562102
Cook, Sanchez-Carbente, Lachance, Radzioch, Tremblay, Khandjian, DesGroseillers, Murai: Fragile X related protein 1 clusters with ribosomes and messenger RNAs at a subset of dendritic spines in the mouse hippocampus. in PLoS ONE 2011
Human Polyclonal PAK1 Primary Antibody für IF, IHC - ABIN362773
Rashid, Banerjee, Nikolic: Phosphorylation of Pak1 by the p35/Cdk5 kinase affects neuronal morphology. in The Journal of biological chemistry 2001
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Human Polyclonal PAK1 Primary Antibody für ELISA, WB - ABIN188561
Zhao, Ma, Calon, Harris-White, Yang, Lim, Morihara, Ubeda, Ambegaokar, Hansen, Weisbart, Teter, Frautschy, Cole: Role of p21-activated kinase pathway defects in the cognitive deficits of Alzheimer disease. in Nature neuroscience 2006
Human Polyclonal PAK1 Primary Antibody für ICC, IF - ABIN4343458
Geiger, Velic, Macek, Lundberg, Kampf, Nagaraj, Uhlen, Cox, Mann: Initial quantitative proteomic map of 28 mouse tissues using the SILAC mouse. in Molecular & cellular proteomics : MCP 2013
results represent the first evidence that Pak1 links extracellular signals to the genetic cascade of transcription factors necessary for cranial neural crest specification
These findings expand the role of phosphoinositides in kinase signaling and suggest how altered phosphoinositide metabolism may upregulate Pak1 activity in cancer cells.
The data suggest that EphA4 activation sequesters active Cdc42 (zeige CDC42 Antikörper) and in this way down-regulates cell-cell adhesion.
Pak1 inhibition interferes with the guidance of mesendoderm migration by directional cues residing in the extracellular matrix of the blastocoel roof, and with mesendoderm translocation in the embryo.
Once activated, c-Abl (zeige ABL1 Antikörper) kinase regulated the activity of Vav1 (zeige VAV1 Antikörper), which further affected Rac1 (zeige RAC1 Antikörper)/PAK1/LIMK1 (zeige LIMK1 Antikörper)/cofilin (zeige CFL1 Antikörper) signaling pathway.
The nuclear functions of PAK1 and its role in the regulation of DNA damage repair is reviewed.
PAK1 is upregulated in cutaneous T cell lymphoma. PAK1 silencing induced apoptosis and inhibited cell growth by stimulating the expression of PUMA (zeige BBC3 Antikörper) and p21 (zeige CDKN1A Antikörper).
Results show that JMJD6 (zeige JMJD6 Antikörper) regulates the alternative splicing of PAK1 in melanoma cells.
PAK1 expression, evaluated by immunohistochemistry, was positively correlated with pERK (zeige EIF2AK3 Antikörper) and beta-catenin (zeige CTNNB1 Antikörper) expression in lung tumors. Patients with high-PAK1, high-pERK (zeige EIF2AK3 Antikörper), and high-nuclear beta-catenin (zeige CTNNB1 Antikörper) tumors more frequently showed an unfavorable response to cisplatin-based chemotherapy when compared to their counterparts.
PKC-zeta (zeige PRKCZ Antikörper) may be responsible for the abnormal growth, proliferation, and migration of metastatic LOVO colon cancer cells via PKC-zeta (zeige PRKCZ Antikörper)/Rac1 (zeige RAC1 Antikörper)/Pak1/beta-Catenin (zeige CTNNB1 Antikörper) pathway.
High expression of PAK1 is associated with invasion of gastric cancer.
Molecular modelling studies of PAK1 with its major interacting partners RHOA (zeige RHOA Antikörper) and STAT3 (zeige STAT3 Antikörper) revealed potential network gene elements in breast invasive carcinoma.
miR4855p reverses EMT (zeige ITK Antikörper) and promotes cisplatin-induced cell death by targeting PAK1 in oral tongue squamous cell carcinoma. This study suggests that PAK1 plays an essential role in the progression of OSCC and it is a potential therapeutic target for OSCC.
Because reduced PAK1 activity impaired FA/BRCA function, inhibition of this kinase in PAK1 amplified and/or overexpressing breast cancer cells represents a plausible strategy for expanding the utility of PARP (zeige COL11A2 Antikörper) inhibitors to FA/BRCA-proficient cancers.
Serine/threonine-protein kinase (zeige HIPK2 Antikörper) proteins, also known as P21 (zeige D4S234E Antikörper)-activated kinase (PAK), and the mechanosensitive factor, Yes-associated protein 1 (YAP-1 (zeige YAP1 Antikörper)) are core mediators of pro-fibrotic integrin beta-1 (zeige ITGB1 Antikörper) signaling.
activated Pak1 regulates chromatin condensation by promoting H3 Ser (zeige SIGLEC1 Antikörper)(10) phosphorylation in oocytes after the resumption of meiotic progression
Depletion of active PAK1 up-regulates the immune system of APC (zeige APC Antikörper)(14/+) mice and suppresses intestinal tumour development. These observations suggest an important role for PAK1 in the immune response to tumours.
Because reduced PAK1 activity impaired FA/BRCA function, inhibition of this kinase in PAK1 amplified and/or overexpressing breast cancer cells represents a plausible strategy for expanding the utility of PARP (zeige PARP1 Antikörper) inhibitors to FA/BRCA-proficient cancers.
Results from our analysis showed that Pak1 overexpression, knockdown and Pak1 knockout cell line models showed that Pak1 confers protection to keratinocytes from UV-B-induced apoptosis and DNA damage via ATR
These results establish a novel signaling process whereby PAK1 upregulates COX-2 (zeige COX2 Antikörper), reduces anandamide levels and restricts tonic endocannabinoids-mediated processes.
The findings suggest that PAK1 deficiency may underlie an increased diabetic susceptibility. Discovery of ways to remediate glycaemic dysregulation via altering PAK1 or its downstream effectors offers promising opportunities for disease intervention.
present work presents the correlation between DSCAM gene overexpression and a dysregulation of the PAK pathway, resulting in altered morphological parameters of neuronal plasticity in the trisomic cell line, namely decreased number and length of processes
These results identify Pak1 and Pak2 (zeige PAK2 Antikörper) as redundant regulators of myoblast differentiation in vitro and in vivo and as components of the promyogenic Ncad (zeige CDH2 Antikörper)/Cdo (zeige CDO1 Antikörper)/Cdc42 (zeige CDC42 Antikörper) signaling pathway.
PAK-mediated phosphorylation of PKD1 at Ser203 triggers its membrane dissociation and subsequent entry into the nucleus, thereby regulating the phosphorylation of PKD1 nuclear targets, including class IIa histone deacetylases.
FOXO-Pak1 pathway was recently shown to regulate mammalian neuronal polarity, our findings indicate that the roles of FOXO and Pak1 in neuronal migration are most likely conserved from C. elegans to higher organisms.
PAK1 promotes reproduction, whereas it inactivates HSP16.2 gene and shortens lifespan.
Pak-1 interacts with Wnt (zeige WNT2 Antikörper) signaling to regulate tissue polarity and gene expression.
only PAK-1 functions in the GIT/PIX (zeige ARHGEF7 Antikörper)/PAK pathway independently of RAC (zeige AKT1 Antikörper)/CDC42 (zeige CDC42 Antikörper) GTPases.
Data show that combined loss of ROCK and PAK, or ROCK and MRCK (zeige CDC42BPA Antikörper), completely prevented embryonic elongation, but a constitutively active form of MLC-4 could only rescue a lack of MRCK (zeige CDC42BPA Antikörper).
This gene encodes a family member of serine/threonine p21-activating kinases, known as PAK proteins. These proteins are critical effectors that link RhoGTPases to cytoskeleton reorganization and nuclear signaling, and they serve as targets for the small GTP binding proteins Cdc42 and Rac. This specific family member regulates cell motility and morphology. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
p21 GTPase-associated kinase 1
, p21-activated kinase 1
, p21/Cdc42/Rac1-activated kinase 1 (STE20 homolog, yeast)
, putative CDKN1A-activated kinase 1
, STE20 homolog, yeast
, p21/Cdc42/Rac1-activated kinase 1 (yeast Ste20-related)
, serine/threonine-protein kinase PAK 1
, CDC42/RAC effector kinase PAK-A
, activated protein kinase alpha
, p21 (CDKN1A)-activated kinase 1
, protein kinase MUK2