Potassium+4-(ethylthio)phenyltrifluoroborate
Catalog Number:
(77048-970)
Supplier:
ANTIBODIES.COM LLC
Description:
Rabbit polyclonal antibody to alpha 1 Sodium Potassium ATPase (phospho Tyr260) for WB and ELISA with samples derived from Human, Mouse and Rat.
Catalog Number:
(10274-934)
Supplier:
Bioss
Description:
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Catalog Number:
(10274-938)
Supplier:
Bioss
Description:
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Catalog Number:
(10336-594)
Supplier:
Bioss
Description:
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
Catalog Number:
(10349-076)
Supplier:
Bioss
Description:
Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Supplier:
Ricca Chemical
Description:
Potassium Acid Phthalate, 300 mg/L, Multi-Purpose Standard, Ricca Chemical Company
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Catalog Number:
(76011-878)
Supplier:
Prosci
Description:
This gene encodes a member of the inwardly rectifying potassium channel family of proteins. Members of this family form ion channel pores that allow potassium ions to pass into a cell. The encoded protein belongs to a subfamily of low signal channel conductance proteins that have a low dependence on potassium concentration. Mutations in this gene are associated with snowflake vitreoretinal degeneration. Alternate splicing results in multiple transcript variants.
Supplier:
Thermo Scientific Chemicals
Description:
ATP-dependent potassium channel (KATP) and cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel blocker
Catalog Number:
(77442-728)
Supplier:
Teknova
Description:
PBS 1X Solution composition: 137.0 mM Sodium chloride, 4.3 mM sodium phosphate dibasic, 2.7 mM potassium chloride, 1.4 mM potassium phosphate monobasic and 0.1% Tween 80.
Supplier:
Bel-Art Products
Description:
Excellent for sampling from tank cars, tank trucks and barges, these samplers are well suited for sodium hydroxide, potassium hydroxide, hydrochloric acid, acetic acid, formaldehyde, sulfuric acid, etc.
Catalog Number:
(66170-814)
Supplier:
LaMotte
Description:
Potassium chloride solutions can be used to standardize conductivity meters
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Catalog Number:
(80085-302)
Supplier:
WTW
Description:
For Potassium Ion Selective Electrode K 800.
Supplier:
Ricca Chemical
Description:
Potassium Permanganate Standard, 89.1 mg/L, equivalent to 100 mg/L (ppm) Clâ‚‚, Ricca Chemical Company
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Catalog Number:
(10275-812)
Supplier:
Bioss
Description:
Voltage-gated K+ channels in the plasma membrane are important regulators of electrical signaling, controlling the repolarization and the frequency of action potentials in neurons, muscles and other excitable cells. KCNT2 is a 1,135 amino acid multi-pass transmembrane protein belonging to the potassium channel family (calcium-activated subfamily) of proteins. KCNT2 produces rapidly activating outward rectifier potassium currents in reponse to high intracellular sodium and chloride levels. Its channel activity is inhibited by ATP, inhalation anesthetics, such as isoflourane, and upon stimulation of G-protein coupled receptors, such as mAChR M1 and GluR-1. There are four isoforms of KCNT2 that are produced as a result of alternative splicing events.
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