You Searched For: Potassium+manganate

Catalog Number: (RC184716)

Supplier: Ricca Chemical

Description: Potassium phthalate in water.

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Catalog Number: (CA27565-49)

Supplier: Hach

Description: Potassium Chloride (KCl) 3 M.

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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: (10336-592)

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: (76120-936)

Supplier: Bioss

Description: This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins, which belong to the recoverin branch of the EF-hand superfamily. Members of this family are small calcium binding proteins containing EF-hand-like domains. They are integral subunit components of native Kv4 channel complexes that may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. The encoded protein also functions as a calcium-regulated transcriptional repressor, and interacts with presenilins. Alternatively spliced transcript variants encoding different isoforms have been described.

Catalog Number: (76120-934)

Supplier: Bioss

Description: This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins, which belong to the recoverin branch of the EF-hand superfamily. Members of this family are small calcium binding proteins containing EF-hand-like domains. They are integral subunit components of native Kv4 channel complexes that may regulate A-type currents, and hence neuronal excitability, in response to changes in intracellular calcium. The encoded protein also functions as a calcium-regulated transcriptional repressor, and interacts with presenilins. Alternatively spliced transcript variants encoding different isoforms have been described.

Supplier: Thermo Scientific Chemicals

Description: A potassium channel antagonist which blocks the postischemic effects of the potassium channel activator cromakalim

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Supplier: Thermo Scientific Chemicals

Description: A potassium channel blocker

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Supplier: Thermo Scientific Chemicals

Description: Stab. with potassium carbonate

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Catalog Number: (CA603-111-126)

Supplier: Rockland Immunochemical

Description: 1mg. Minimum cross reactivity. Antibody Concentration: 1 mg/mL. Fluorochrome/Protein: 5.7 moles Cy2 per mole of goat IgG. Buffer: 0.02M potassium phosphate, 0.15M sodium chloride, pH 7.2. Lyophilized.

Supplier: Thermo Scientific Chemicals

Description: A potassium channel blocker

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Supplier: Thermo Scientific Chemicals

Description: 0.0035 M

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Catalog Number: (CA001-0033)

Supplier: Rockland Immunochemical

Description: 1mg. Antibody Concentration: 1 mg/mL. Fluorochrome/Protein: 4 moles TRITC per mole of Bovine Albumin. Buffer: 0.02M potassium phosphate, 0.15M sodium chloride, pH 7.2. Stabilizer: 10 mg/mL polyethylene glycol. For research. Lyophilized.

Supplier: Rockland Immunochemical

Description: 1.0mg. Liquid (sterile filtered). Streptavidin Concentration: 1.0 mg/ml (by UV absorbance at 280 nm). Buffer: 0.02M Potassium Phosphate, 0.15M Sodium Chloride, 0.01M Magnesium Chloride, pH 7.2. Preservative: 0.01% (w/v) Sodium Azide

Supplier: Thermo Scientific Chemicals

Description: Stab. with 0.1% potassium hydroxide

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Catalog Number: (10336-596)

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]