You Searched For: Acetylcholine+iodide

Catalog Number: (PRSI31-097)

Supplier: ProSci Inc.

Description: Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels nAChRs are pentameric structures that are made up of combinations of individual subunits. CHRNB3 is one of the subunits of nAChR. Twelve neuronal nAChR subunits have been described, alpha2-alpha10 and beta2-beta4. CHRNB3 decreased the channel mean open time and burst length. There was also an increase in single channel slope conductance. On the other hand, the calcium permeability and the pharmacological properties of beta3-containing receptors differed little from those of without beta3. Dysfunction of nAChR has been linked to a number of human diseases such as schizophrenia, Alzheimer's and Parkinson's diseases. nAChRs also play a significant role in nicotine addiction.

UOM: 1 * 50 µG

Catalog Number: (PRSI25-026)

Supplier: ProSci Inc.

Description: PHOX2A contains a paired-like homeodomain most similar to that of the Drosophila aristaless gene product. The encoded protein plays a central role in development of the autonomic nervous system. It regulates the expression of tyrosine hydroxylase and dopamine beta-hydroxylase, two catecholaminergic biosynthetic enzymes essential for the differentiation and maintenance of the noradrenergic neurotransmitter phenotype. PHOX2A has also been shown to regulate transcription of the alpha3 nicotinic acetylcholine receptor gene.The protein encoded by this gene contains a paired-like homeodomain most similar to that of the Drosophila aristaless gene product. The encoded protein plays a central role in development of the autonomic nervous system. It regulates the expression of tyrosine hydroxylase and dopamine beta-hydroxylase, two catecholaminergic biosynthetic enzymes essential for the differentiation and maintenance of the noradrenergic neurotransmitter phenotype. The encoded protein has also been shown to regulate transcription of the alpha3 nicotinic acetylcholine receptor gene. Mutations in this gene have been associated with autosomal recessive congenital fibrosis of the extraocular muscles. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

UOM: 1 * 50 µG

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: (84723.0001)

Supplier: VWR Chemicals

Description: The isolation of microorganisms often requires the use of specific supplements. The supplements presented here are available in vials and bottles, and the corresponding culture medium to use with them is indicated in the table below. Usually each vial is used to supplement 500 ml of media unless otherwise stated (complete information available on the specification sheets available on request).

UOM: 1 * 50 mL

Certificates

Catalog Number: (705-0080)

Supplier: Hach

Description: Potassium iodide

UOM: 1 * 50 items

Catalog Number: (MOLE65234485-100G)

Supplier: Molekula

Description: Tetrapropylammonium iodide

UOM: 1 * 100 g

 This is a MarketSource item. Additional charges may apply

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

Supplier: Alfa Aesar

Description: Erbium triiodide, ultra dry ≥99.9% (REO, rare earth oxide basis)

Catalog Number: (PRSI91-705)

Supplier: ProSci Inc.

Description: Cysteine-Rich with EGF-Like Domain Protein 2 (CRELD2) is a secreted protein that is a member of the CRELD family. Human CRELD2 is synthesized as a 353 amino acid precursor protein with a signal peptide, a highly conserved domain rich in glutamic acid and tryptophan (WE) and EGF-like repeats. CRELD2 is ubiquitously expressed in many tissues. CRELD2 may interact with CHRNA4 and regulate transport of alpha4- beta 2 neuronal acetylcholine receptor. In addition, CRELD2 could be a novel mediator in regulating the onset and progression of various ER stress-associated diseases.

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: (MOLE36409596-1KG)

Supplier: Molekula

Description: Potassium iodide

UOM: 1 * 1 kg

 This is a MarketSource item. Additional charges may apply

Supplier: Roth Carl

Description: Potassium iodide

Catalog Number: (MOLEM82850263)

Supplier: Molekula

Description: Trimethylsulphoxonium iodide

UOM: 1 * 500 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (MOLE11076392-100G)

Supplier: Molekula

Description: (Ethyl)triphenylphosphonium iodide

UOM: 1 * 100 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (MOLE10687936-25G)

Supplier: Molekula

Description: Benzyltrimethylammonium iodide

UOM: 1 * 25 g

 This is a MarketSource item. Additional charges may apply

Catalog Number: (ICNA0210122805)

Supplier: MP Biomedicals

Description: D-Pantothenic acid is an essential vitamin (except in horses, ruminants). Pantothenic acid is involved in a number of biological reactions including: A precursor in the biosynthesis of coenzyme A, production of energy, catabolism of fatty acids and amino acids, synthesis of fatty acids, phospholipids, sphingolipids, cholesterol and steroid hormones, synthesis of heme and the neurotransmitter acetylcholine and involved in regulation of gene expression and in signal transduction.

UOM: 1 * 5 g