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SLC12A6 is a member of the K-Cl cotransporter (KCC) family. Zusätzlich bieten wir Ihnen Solute Carrier Family 12 (Potassium-Chloride Transporter) Member 6 Proteine (9) und Solute Carrier Family 12 (Potassium-Chloride Transporter) Member 6 Kits (1) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 73 products:
Human Polyclonal SLC12A6 Primary Antibody für ELISA, WB - ABIN564298
Salin-Cantegrel, Shekarabi, Holbert, Dion, Rochefort, Laganière, Dacal, Hince, Karemera, Gaspar, Lapointe, Rouleau: HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3. in Human molecular genetics 2008
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Human Polyclonal SLC12A6 Primary Antibody für IHC, ELISA - ABIN238578
Simard, Bergeron, Frenette-Cotton, Carpentier, Pelchat, Caron, Isenring: Homooligomeric and heterooligomeric associations between K+-Cl- cotransporter isoforms and between K+-Cl- and Na+-K+-Cl- cotransporters. in The Journal of biological chemistry 2007
Human Polyclonal SLC12A6 Primary Antibody für ICC, IF - ABIN4328465
Shiozaki, Takemoto, Ichikawa, Fujiwara, Konishi, Kosuga, Komatsu, Okamoto, Kishimoto, Marunaka, Otsuji: The K-Cl cotransporter KCC3 as an independent prognostic factor in human esophageal squamous cell carcinoma. in BioMed research international 2014
These results suggest that the expression of KCC3 in ESCC may affect cellular invasion and be related to a worse prognosis in patients with ESCC.
SPAK (zeige STK39 Antikörper) may promote KCC3-mediated cervix tumor aggressiveness via the NF-kappaB (zeige NFKB1 Antikörper)/p38 MAPK (zeige MAPK14 Antikörper)/MMP2 (zeige MMP2 Antikörper) axis.
SLC12A6 has been shown to be causative in Andermann Syndrome.
serine residue 96 of human KCC3 is a third site that has to be dephosphorylated for full activation of the cotransporter during hypotonicity.
mis (zeige AMH Antikörper)-trafficking of mutant protein is an important pathophysiological feature of HMSN/ACC (zeige ACACA Antikörper) causative KCC3 mutations.
Neuropathic features of hereditary motor and sensory neuropathy/agenesis of corpus callosum in transgenic mouse lines are predominantly due to a neuronal KCC3 deficit, while the auditory impairment is due to loss of non-neuronal KCC3 expression.
The Wnk3 (zeige WNK3 Antikörper) protein isoforms have a similar effect on SLC12 cotransporters. NKCC1 (zeige SLC12A2 Antikörper)/2 and NCC (zeige SLC12A3 Antikörper) were inhibited, even in hypertonicity, while KCCs were activated, even in isotonic conditions.
KCC3 is the dominant isoform in erythrocytes, with variable expression of KCC1 (zeige SLC12A4 Antikörper) and KCC4 (zeige SLC12A7 Antikörper) that could result in modulation of KCC activity
mutations of the KCC3 gene may result in non-syndromic childhood onset of demyelinating hereditary motor and sensory neuropathy
all of the CCCs examined (NKCC1 (zeige SLC12A2 Antikörper), NKCC2 (zeige SLC12A1 Antikörper), KCC1 (zeige SLC12A4 Antikörper), KCC3, and KCC4 (zeige SLC12A7 Antikörper)) can promote NH4(+) translocation, presumably through binding of the ion at the K(+) site
Kcc3 inactivation caused systemic vascular resistance and ventricular mass to increase while preventing extracellular fluid volume to accumulate.
The results establish that the parvalbumin (zeige PVALB Antikörper)-positive neuronal population is an important player in the pathogenic development of peripheral neuropathy associated with agenesis of the corpus callosum.
Data are consistent with a role for KCC3 in the proximal tubule glucose reabsorption mechanism.
KCC3 regulates NADPH oxidase (zeige NOX1 Antikörper) activity and neutrophils activation
KCC3 contributes to Cl(-) extrusion in adult sensory neurons
K+-Cl-cotransporter (zeige SLC12A4 Antikörper) KCC3 is expressed in neurons, interneurons and radial glial-like cells in the spinal cord.
This study demonstrated that the K(+)-Cl(-) cotransporter (zeige SLC12A4 Antikörper) activity of KCC3 contributes to the propagation of action potentials along peripheral nerves.
Expression of Slc12a6 in the mouse nucleus accumbens is modulated by a sequence variant (B2 SINE indel) in the 3' UTR (zeige UTS2R Antikörper) of Comt (catechol-O-methyltransferase (zeige COMT Antikörper)).
SLC12A6 has a role in the development and maintenance of the nervous system
This gene is a member of the K-Cl cotransporter (KCC) family. K-Cl cotransporters are integral membrane proteins that lower intracellular chloride concentrations below the electrochemical equilibrium potential. The proteins encoded by this gene are activated by cell swelling induced by hypotonic conditions. Alternate splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are associated with agenesis of the corpus callosum with peripheral neuropathy.
solute carrier family 12 member 6
, furosemide-sensitive KCl cotransporter 3
, K-Cl cotransporter 3
, electroneutral potassium-chloride cotransporter 3
, potassium chloride cotransporter 3
, potassium chloride cotransporter KCC3a-S3
, potassium-chloride transporter-3a
, potassium-chloride transporter-3b
, solute carrier family 12 (potassium/chloride transporters), member 6