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Potassium tetracyanonickelate(II) hydrate

Supplier: Thermo Scientific Chemicals
Description: Soluble in water

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Image Unavailable-CAAA39307-30

Mercury (II) potassium iodide

Catalog Number: (CAAA39307-30)
Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00049656

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Image Unavailable-77991-960

TRC Potassium Tetrachloroplatinum(II)

Catalog Number: (77991-960)
Supplier: LGC Standards
Description: TRC Potassium Tetrachloroplatinum(II)

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Product Image-RC300032

Fehling's reagent II (L(+)-potassium sodium tartrate in sodium hydroxide solution) for quantitative determination of reducing sugars

Supplier: Ricca Chemical
Description: Fehling Solution B. AOAC. EPA for determination of reducing sugars. Use with Fehling's Copper Solution. Group No.3010. Container: Plastic.

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Dipotassium tetrabromopalladate Pd 20,0%

Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00049659

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Product Image-CAAA11885-04

Dipotassium tetrachloropalladate ≥99.99% (metals basis) Pd ≥ 32.2%, Premion®

Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00011373

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Product Image-RC5260-16

Nessler reagent Folin-Wu Modified for determination of non-protein nitrogen (NPN)

Catalog Number: (RC5260-16)
Supplier: Ricca Chemical
Description: Folin-Wu modified for determination of non-protein nitrogen.

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Product Image-RC525032

Nessler reagent USP XXV

Supplier: Ricca Chemical
Description: (Mercuric - Potassium Iodide TS, Alkaline), USP 25 Formulation

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Image Unavailable-TCB1124-005G

5-Mercapto-3-phenyl-1,3,4-thiadiazole-2(3H)thione potassium salt ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: CAS Number: 6336-51-2
MDL Number: MFCD00014092
Molecular Formula: C8H5KN2S3
Molecular Weight: 264.42
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Storage Temperature: 0-10°C

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Product Image-RC314016

Ferroin (1,10-phenanthrolineferrous sulfate complex) 0.025 M in aqueous solution indicator

Supplier: Ricca Chemical
Description: APHA, ASTM. For use with ceric sulfate, iron (II) ammonium sulfate and potassium dichromate titrants.

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Image Unavailable-76098-952

Anti-Kir6.2 (KCNJ11) Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76098-952)
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. .
Image Unavailable-10336-598

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10336-598)
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]
Image Unavailable-76098-950

Anti-Kir6.2 (KCNJ11) Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76098-950)
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. .
Image Unavailable-10336-922

Anti-KCNJ11 Rabbit Polyclonal Antibody

Catalog Number: (10336-922)
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]
Image Unavailable-10336-596

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy5.5®)

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]
Image Unavailable-10336-600

Anti-KCNJ11 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10336-600)
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]
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