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Hledali jste: Potassium+tetranitroplatinate(II)


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Dodavatel: VWR Chemicals
Popis: 6 components: Lithium (Li+) 50 mg/l, Sodium (Na+) 200 mg/l, Ammonium (NH4+) 250 mg/l, Potassium (K+) 500 mg/l, Calcium (Ca2+) 500 mg/l, Magnesium (Mg2+) 250 mg/l in H₂O
Dodavatel: Thermo Fisher Scientific
Popis: Tetrachlorplatnatan draselný 99.99% (trace metals basis)
Dodavatel: Thermo Fisher Scientific
Popis: Dipotassium tetrachloropalladate > 32,0% Pd
Katalogové číslo: (87815.290)
Dodavatel: VWR Chemicals
Popis: Starting materials:
Solution A. Copper sulfate R/ Water R
Solution B. anhydrous Sodium carbonate R / Potassium sodium tartrate R/ Sodium hydrogen carbonate R/ anhydrous Sodium sulfate R/ Water R
Měrná jednotka: 1 * 1 L

Dodavatel: Thermo Fisher Scientific
Popis: Dipotassium tetrachloropalladate ≥99.99% (metals basis) Pd ≥ 32.2%, Premion®
Dodavatel: PanReac AppliChem
Popis: Suitable for nitrogen determination.

New Product

Katalogové číslo: (SIAL281557-1G)
Dodavatel: Merck
Popis: Potassium tetracyanoplatinate(II), Sigma-Aldrich®
Měrná jednotka: 1 * 1 g


Katalogové číslo: (BOSSBS-2436R)
Dodavatel: Bioss
Popis: 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]
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-12181R-CY5)
Dodavatel: Bioss
Popis: 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]
Měrná jednotka: 1 * 100 µl


Dodavatel: Merck
Popis: Potassium hexacyanoruthenate(II) hydrate, Sigma-Aldrich®

Katalogové číslo: (35585.K2)
Dodavatel: Thermo Fisher Scientific
Popis: Potassium hexacyanoferrate(II) standardised solution 0.1 N in aqueous solution Standard Volumetric Solution
Měrná jednotka: 1 * 1 L

Katalogové číslo: (SIAL281565-1G)
Dodavatel: Merck
Popis: Potassium tetracyanoplatinate(II) hydrate ≥98%, crystalline, Sigma-Aldrich®
Měrná jednotka: 1 * 1 g


Katalogové číslo: (BOSSBS-2436R-HRP)
Dodavatel: Bioss
Popis: 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]
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-12181R-FITC)
Dodavatel: Bioss
Popis: 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]
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-12181R-HRP)
Dodavatel: Bioss
Popis: 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]
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-2436R-A750)
Dodavatel: Bioss
Popis: 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 characterised 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.
Měrná jednotka: 1 * 100 µl


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Omezené množství produktu na skladě. Zboží může být k dispozici v jiném skladě poblíž vašeho sídla. Přesvědčte se, že jste přihlášení na stránky, abyste mohli vidět dostupné položky na skladě. Pokud je stále zobrazeno call a potřebujete asistenci, volejte na číslo 321 570 321.
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