You Searched For: Retigabine+dihydrochloride

Supplier: Thermo Scientific

Description: Retigabine dihydrochloride

Catalog Number: (90221-25MG)

Supplier: Merck

Description: Organic Standard, Retigabine

UOM: 1 * 25 mg

Catalog Number: (R-018-1ML)

Supplier: Merck

Description: Organic Standard, Retigabine solution, ampoule of 1 ml

UOM: 1 * 1 mL

Catalog Number: (PRSI28-294)

Supplier: ProSci Inc.

Description: The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by KCNQ2 and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in KCNQ2 are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1).The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by this gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in this gene are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1). At least five transcript variants encoding five different isoforms have been found for this gene.

UOM: 1 * 50 µG

Catalog Number: (PRSI28-295)

Supplier: ProSci Inc.

Description: The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by the KCNQ2 gene and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in KCNQ2 are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1).

UOM: 1 * 100 µG

Catalog Number: (PRSI28-293)

Supplier: ProSci Inc.

Description: The M channel is a slowly activating and deactivating potassium channel that plays a critical role in the regulation of neuronal excitability. The M channel is formed by the association of the protein encoded by KCNQ2 and a related protein encoded by the KCNQ3 gene, both integral membrane proteins. M channel currents are inhibited by M1 muscarinic acetylcholine receptors and activated by retigabine, a novel anti-convulsant drug. Defects in KCNQ2 are a cause of benign familial neonatal convulsions type 1 (BFNC), also known as epilepsy, benign neonatal type 1 (EBN1).

UOM: 1 * 50 µG

Catalog Number: (D2679-1VL)

Supplier: Merck

Description: O-Dianisidine dihydrochloride, Supelco®

UOM: 1 * 1 items

Catalog Number: (8.20575.0001)

Supplier: Merck

Description: 2,7-Diaminofluorene dihydrochloride

UOM: 1 * 1 g

Supplier: Merck

Description: Cystamine dihydrochloride, Sigma-Aldrich®

Supplier: Merck

Description: Hydrazine dihydrochloride for synthesis, Sigma-Aldrich®

Supplier: Merck

Description: 2,4-Diaminophenol dihydrochloride for synthesis, Sigma-Aldrich®

Supplier: Merck

Description: 1,4-Diaminobutane dihydrochloride, Sigma-Aldrich®

Catalog Number: (T3134-5G)

Supplier: SIGMA ALDRICH MICROSCOPY

Description: N,N,N',N'-Tetramethyl-p-phenylenediamine dihydrochloride ≥95%, powder, Sigma-Aldrich®

UOM: 1 * 5 g

Supplier: Merck

Description: N-(1-Naphthyl)ethylenediamine dihydrochloride ACS analytical reagent, Supelco®

Supplier: Merck

Description: N-(1-Naphthyl)ethylenediamine dihydrochloride, Supelco®

Catalog Number: (8.14609.0010)

Supplier: Merck

Description: Formamidine disulphide dihydrochloride for synthesis, Sigma-Aldrich®

UOM: 1 * 10 g