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STK39 encodes a serine/threonine kinase that is thought to function in the cellular stress response pathway. Zusätzlich bieten wir Ihnen STK39 Kits (21) und STK39 Proteine (7) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal STK39 Primary Antibody für IHC (p), WB - ABIN392497
Liedtke, Wang, Smallwood: Role for protein phosphatase 2A in the regulation of Calu-3 epithelial Na+-K+-2Cl-, type 1 co-transport function. in The Journal of biological chemistry 2005
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Human Polyclonal STK39 Primary Antibody für ELISA, IHC - ABIN4356620
Ramoz, Cai, Reichert, Silverman, Buxbaum: An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene. in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008
Here, we report our replication data showing a significant association of the rs3754777 polymorphism, but not rs35929607, of STK39 with essential hypertension in a male Chinese Han population.
Both SPAK and OSR1 (zeige OXSR1 Antikörper) kinases entering cells through exosomes are preferentially expressed at the plasma membrane and that the kinases in exosomes are functional and maintain NKCC1 (zeige SLC12A2 Antikörper) in a phosphorylated state.
did not observe any significant difference in allele and genotype distribution between Parkinson's disease patients and controls for rs1955337 in STK39
SPAK and OSR1 (zeige OXSR1 Antikörper) are both stimulators of Kir2.1 (zeige KCNJ2 Antikörper) activity.
SPAK and OSR1 (zeige OXSR1 Antikörper) are powerful stimulators of the intestinal Na+-coupled phosphate co-transporter NaPi-IIb (zeige SLC34A2 Antikörper)
Single nucleotide polymorphisms STK39 and WNK1 (zeige WNK1 Antikörper) were associated with hypertension and BP in our multicenter Belgian case-control study
STK39 mRNA and protein express abnormally in primary hypertension patients with genetic variation, which is related to the blood pressure.
SPAK protein has both the potential to up-regulate KCNQ1 (zeige KCNQ1 Antikörper)/E1 protein abundance in the cell membrane, an effect possibly participating in the regulation of cell volume, excitability, epithelial transport and metabolism.
SPAK and OSR1 (zeige OXSR1 Antikörper) are powerful negative regulators of the excitatory glutamate (zeige GRIN1 Antikörper) transporters EAAT1 (zeige SLC1A3 Antikörper) and EAAT2 (zeige SLC1A2 Antikörper).
SPAK and OSR1 (zeige OXSR1 Antikörper) are negative regulators of EAAT3 (zeige SLC1A1 Antikörper) activity
SPAK plays a pathogenic role in IgA nephropathy through the activation of NF-kappaB (zeige NFKB1 Antikörper)/MAPK (zeige MAPK1 Antikörper) signaling pathway.
Here, we show that specific expression of CA-SPAKwithin the early distal convoluted tubule (DCT1 (zeige SLC11A2 Antikörper)) drives FHHt.
Our data reveal that together SPAK and OSR1 (zeige OSR1 Antikörper) play essential roles in the pathway along the distal convoluted tubules that responds to fluctuations in plasma potassium
Genetic depletion of SPAK kinase reduces ischemic brain injury after occlusion of the left middle cerebral artery.
the increased NCC (zeige SLC12A3 Antikörper) expression and activation is present in CMA which is highly associated with the enhanced WNK4 (zeige WNK4 Antikörper)-SPAK signal pathway using WNK4 (zeige WNK4 Antikörper)-/- and SPAK-/- mice.
We conclude that TRPV2 (zeige TRPV2 Antikörper) is involved in osmosensation in skeletal muscle fibres, acting in concert with P-SPAK-activated NKCC1 (zeige SLC12A2 Antikörper)
SPAK has the potential to up-regulate ENaC (zeige SCNN1A Antikörper)
These observations establish that the CCT (zeige FLVCR2 Antikörper) domain plays a crucial role in controlling SPAK activity and BP.
The data of this study supported the gene-environment hypothesis and demonstrated the potential value of SPAK manipulation in future schizophrenia studies.
The structure of partially active SPAK T243D is consistent with a multistage activation process in which phosphorylation induces a SPAK conformation that requires further remodeling to build the active structure.
This gene encodes a serine/threonine kinase that is thought to function in the cellular stress response pathway. The kinase is activated in response to hypotonic stress, leading to phosphorylation of several cation-chloride-coupled cotransporters. The catalytically active kinase specifically activates the p38 MAP kinase pathway, and its interaction with p38 decreases upon cellular stress, suggesting that this kinase may serve as an intermediate in the response to cellular stress.
serine threonine kinase 39 (STE20/SPS1 homolog)
, serine threonine kinase 39 (STE20/SPS1 homolog, yeast)
, serine threonine kinase 39
, serine/threonine kinase 39
, STE20/SPS1 homolog
, STE20/SPS1-related proline-alanine-rich protein kinase
, Ste20-like protein kinase
, proline-alanine-rich STE20-related kinase
, serine/threonine-protein kinase 39
, small intestine SPAK-like kinase
, ste-20-related kinase
, Ste-20 related kinase
, pancreatic serine/threonine-protein kinase
, kidney-specific SPAK
, serine/threonine kinase 39, STE20/SPS1 homolog