You Searched For: Potassium+tetrabromoplatinate+(II)


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Supplier: Alfa Aesar
Description: Potassium tetracyanoplatinate(II) trihydrate is used in the preparation other salts like Krogmann's salt, that are highly conducting, one dimensional materials.

Catalog Number: (87709.200)
Supplier: VWR Chemicals
Description: Nessler reagent solutions (I+II) [Potassium Iodomercurate solution + NaOH 25% w/v solution] Reag. Ph. Eur. 1071600 for determination of ammonia and ammonium salts
UOM: 1 * 200 mL

Supplier: Merck
Description: Determination of ammonium/nitrogen salts using mercury containing materials.
Supplier: Thermo Scientific
Description: Fehling's reagent II (L(+)-potassium sodium tartrate in sodium hydroxide solution)

Catalog Number: (31074.265)
Supplier: VWR Chemicals
Description: Nessler reagent for determination of ammonia and ammonium salts
UOM: 1 * 500 mL

Supplier: VWR Chemicals
Description: 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

Supplier: Cayman Chemical
Description: Angiotensin II is a hormone that plays an important role in regulating blood pressure.

Catalog Number: (87815.290)
Supplier: VWR Chemicals
Description: 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
UOM: 1 * 1 L

Supplier: Alfa Aesar
Description: Dipotassium tetrabromopalladate (20,0% Pd)

Supplier: Thermo Scientific
Description: Dipotassium tetrachloropalladate > 32,0% Pd

Catalog Number: (BLDPBD148912-1G)
Supplier: BLD PHARMATECH GMBH
Description: Dipotassium tetrachloropalladate 99.99%
UOM: 1 * 1 g


Supplier: Alfa Aesar
Description: Dipotassium tetrachloropalladate ≥99.99% (metals basis) Pd ≥ 32.2%, Premion®

Supplier: SIGMA ALDRICH MICROSCOPY
Description: Folin & Ciocalteu's phenol reagent is most commonly used in the Lowry method for determining protein concentration. It has also been used for the quantification of total phenolics. In this method, protein is pretreated with copper(II) in a modified biuret reagent (alkaline copper solution
stabilized with sodium potassium tartrate). Addition of the phenol reagent generates chromogens that give increasing absorbance between 550-750nm. Normally, absorbance at the peak (750 nm) or shoulder (660 nm) are used to quantitate protein concentrations between 1 - 100 mg/ml while absorbance at 550 nm is used to quantitate higher protein concentrations.

Catalog Number: (BOSSBS-2436R-FITC)
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]
UOM: 1 * 100 µl


Catalog Number: (BOSSBS-2436R-A555)
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]
UOM: 1 * 100 µl


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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