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You Searched For: 7.2+CPG+[TQ7.2+CPG]


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Image Unavailable-CAAA11883-06

Dipotassium tetrabromopalladate Pd 20,0%

Description: MDL: MFCD00049659
Catalog Number: CAAA11883-06
Supplier: Thermo Scientific Chemicals

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Product Image-CAAA11885-09

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

Description: MDL: MFCD00011373
Catalog Number: CAAA11885-09
Supplier: Thermo Scientific Chemicals

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Product Image-RC525016

Nessler reagent USP XXV

Description: (Mercuric - Potassium Iodide TS, Alkaline), USP 25 Formulation
Catalog Number: RC525016
Supplier: Ricca Chemical

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Product Image-RC5260-16

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

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

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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)

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
Catalog Number: TCB1124-005G
Supplier: TCI America

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Product Image-RC314016

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

Description: APHA, ASTM. For use with ceric sulfate, iron (II) ammonium sulfate and potassium dichromate titrants.
Catalog Number: RC314016
Supplier: Ricca Chemical

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Product Image-BDH9278-500G

Sodium acetate trihydrate 99.0-101.0% ACS, VWR Chemicals BDH®

Description: Meets reagent specifications for testing USP/NF monographs.
Catalog Number: BDH9278-500G
Supplier: VWR International

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Product Image-CAJT2146-0

tetra-Chloroauric(III) acid trihydrate, BAKER ANALYZED® ACS, J.T.Baker®

Description: tetra-Chloroauric(III) acid trihydrate, BAKER ANALYZED® ACS
Catalog Number: CAJT2146-0
Supplier: VWR International

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Product Image-97061-864

Sodium acetate trihydrate ACS

Description: Sodium acetate trihydrate ACS
Catalog Number: 97061-864
Supplier: VWR

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Image Unavailable-10336-594

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy5®)

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: 10336-594
Supplier: Bioss
Image Unavailable-10336-598

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy7®)

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: 10336-598
Supplier: Bioss
Image Unavailable-76098-950

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

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. .
Catalog Number: 76098-950
Supplier: Bioss
Image Unavailable-10339-588

Anti-KCNJ11 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

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: 10339-588
Supplier: Bioss
Image Unavailable-10336-600

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

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: 10336-600
Supplier: Bioss
Image Unavailable-10336-592

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy3®)

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
Image Unavailable-76098-952

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

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. .
Catalog Number: 76098-952
Supplier: Bioss
641 - 656 of 14,196