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The protein encoded by LPPR4 belongs to the lipid phosphate phosphatase (LPP) family. Zusätzlich bieten wir Ihnen Lipid Phosphate Phosphatase-Related Protein Type 4 Kits (7) und viele weitere Produktgruppen zu diesem Protein an.
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RG-1 (zeige PPP1R3A Antikörper)-deficient (KO) mice have deficits in sensorimotor integration and whisker-based sensory discrimination; genetic ablation of PRG-1 (zeige PTGR1 Antikörper) modulates postnatal day 16-19 spontaneous and evoked excitability of the barrel cortex, including enhancement of thalamocortical glutamatergic inputs to Layer 4; data strongly indicate that PRG-1 (zeige PTGR1 Antikörper) is required for the developmental, activity-dependent fine-tuning of sensory cortex function
Endogenous PRG3 (zeige PRG3 Antikörper) promotes neurite shaft protrusion and therefore contributes to regulating filopodia formation in immature neurons.
PRG-1 (zeige PTGR1 Antikörper) as an important player in the modulatory control of hippocampal excitability dependent on presynaptic LPA(2 (zeige LPAR2 Antikörper)) receptor signaling.
Glycosylation as a critical mechanism for PRG-1 (zeige SRGN Antikörper) function was significantly reduced by the PRG (zeige PRB3 Antikörper)-1R346T SNP glycosylation as a critical mechanism
The protein encoded by this gene belongs to the lipid phosphate phosphatase (LPP) family. LPPs catalyze the dephosphorylation of a number of bioactive lipid mediators that regulate a variety of cell functions. This protein is specifically expressed in neurons. It is located in the membranes of outgrowing axons and has been shown to be important for axonal outgrowth during development and regenerative sprouting. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
lipid phosphate phosphatase-related protein type 4
, plasticity related gene 1
, brain-specific phosphatidic acid phosphatase-like protein 1
, plasticity-related gene 1 protein