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Human Polyclonal PPP1R9B Primary Antibody für ELISA, WB - ABIN566586
Sagara, Kawasaki, Iemura, Natsume, Takai, Akiyama: Asef2 and Neurabin2 cooperatively regulate actin cytoskeletal organization and are involved in HGF-induced cell migration. in Oncogene 2009
Clinical onset of AD is marked by the loss of PreC spinophilin-ir dendritic spines that is related to Abeta (zeige APP Antikörper) pathology and may contribute to cognitive symptoms early in the disease.
The increased cancer stem cells-like properties induced by the downregulation of Spn (zeige SPN Antikörper) might account for the increased malignant phenotype observed in Spn (zeige SPN Antikörper)-null breast tumors.
homo-oligomerization of neurabin is required for stabilizing RGS4 (zeige RGS4 Antikörper) on the plasma membrane to attenuate A1R (zeige ADORA1 Antikörper) signaling
Data identify Spn (zeige SPN Antikörper) as a critical adhesion and signaling protein that is essential for modulating glioblastoma cell invasion in the brain microenvironment. Spn (zeige SPN Antikörper) suppresses brain tumor cell invasion, in part, via control of Rac1 GTPase (zeige RACGAP1 Antikörper) activities and invadopodia disassembly. Its C-terminus binds directly to the beta 8 integrin cytoplasmic tail.
results indicate that spinophilin plays an important role in regulating the activity of Group I mGluRs as well as their influence on synaptic activity.
Low spinophilin expression enhances aggressive biological behavior of breast cancer.
Colorectal carcinoma expression of spinophilin expression determines cellular growth, cancer stemness and 5-flourouracil resistance.
spinophilin might play a previously unrecognized role in the pathogenesis of head and neck squamous cell carcinoma
Spn (zeige SPN Antikörper) downregulation contributes to a more aggressive biologic behavior, induces chemoresistance, and is associated with a poorer survival in patients with advanced stages of colorectal carcinoma.
study found a substantial number of hepatocellular carcinomas (HCC (zeige FAM126A Antikörper)) show reduced or absent Spn (zeige SPN Antikörper) expression; the low expression of Spn (zeige SPN Antikörper) in tumour tissue is an independent negative prognostic factor for clinical outcome in HCC (zeige FAM126A Antikörper); spinophilin expression inversely correlates with proliferative activity
two homologs neurabin and spinophilin play important yet distinct roles in the regulation of anxiety- and depression-like behaviors in an age-dependent manner.
COPS5 (zeige COPS5 Antikörper) overexpression reduced spinophilin in both the cortex (19%, p < 0.05) and the hippocampus (20%, p < 0.05), leading to significant deficits in learning and memory skills
RanBP9 overexpression in transgenic mice led to striking reduction in the levels of spinophilin.
Canonical betaAR-mediated signaling coupled to PKA activation results in phosphorylation of spinophilin, disrupting its interaction with alpha2AARs and accelerating alpha2AAR (zeige ADRA2A Antikörper) endocytic responses.
Findings support the concept that the inhibitory effects of SPL (zeige SGPL1 Antikörper) on M3R (zeige CHRM3 Antikörper) activity are mediated by RGS4 (zeige RGS4 Antikörper).
changes in spinophilin/CaMKII (zeige CAMK2G Antikörper) interactomes may contribute to changes in striatal dendritic spine density, morphology, and function during normal postnatal maturation and aging.
these data suggest that spinophilin is an upstream regulator required for normal growth and excitation-contraction coupling, but is dispensable for beta-adrenergic stimulation of adult cardiomyocytes.
Findings suggest that spinophilin restrains Angiotensin II-mediated sympathetic nervous system activation and is an unrecognized molecule with regard to central blood pressure control
We suggest that Spn (zeige SPN Antikörper) may be the tumor suppressor gene located at 17q21.33 acting through Rb regulation.
Spinophilin is a regulatory subunit of protein phosphatase-1 catalytic subunit (PP1\; see MIM 176875) and is highly enriched in dendritic spines, specialized protrusions from dendritic shafts that receive most of the excitatory input in the central nervous system (Allen et al., 1997
, neurabin 2
, neural tissue-specific F-actin-binding protein II
, nuerabin 2
, neurabin II
, protein phosphatase 1, regulatory (inhibitor) subunit 9B
, protein phosphatase 1, regulatory subunit 9B, spinophilin