Human Carbohydrate Sulfotransferase 9 (CHST9) ELISA Kit (96T)

Human Carbohydrate Sulfotransferase 9 (CHST9) ELISA Kit (96T)

Catalog #: TD3262
Availability: In Stock
¥649.00
Detection range: 0.781-50ng/mL    
Sensitivity: 0.25ng/mL    
Type: Traditional CHST9 ELISA kit    
Synonyms: GALNAC4ST-2; GALNAC-4-ST2; N-acetylgalactosamine-4-O-sulfotransferase 2; GalNAc-4-O-sulfotransferase 2
Species: Human
Sample type: serum, plasma, tissue homogenates or other biological fluids.
Experimental method: Sandwich
Shelf life: 12 months
Gene ID: 83539
UniProt ID: Q7L1S5
Components: 1. Pre-coated, ready to use 96-well strip plate 1
2. Plate sealer for 96 wells 2
3. Standard 2
4. Diluents buffer: 1×45 mL
5. Detection Reagent A: 1×120 μL
6. Detection Reagent B: 1×120 μL
7. TMB Substrate: 1×9 mL
8. Stop Solution: 1×6 mL
9. Wash Buffer (30× concentrate): 1×20 mL




Background

The nicotinic acetylcholine receptors (nAChRs) are members of a superfamily of ligand-gated ion channels that mediate fast signal transmission at synapses. The nAChRs are (hetero)pentamers composed of homologous subunits. The subunits that make up the muscle and neuronal forms of nAChRs are encoded by separate genes and have different primary structure. There are several subtypes of neuronal nAChRs that vary based on which homologous subunits are arranged around the central channel. They are classified as alpha-subunits if, like muscle alpha-1 (MIM 100690), they have a pair of adjacent cysteines as part of the presumed acetylcholine binding site. Subunits lacking these cysteine residues are classified as beta-subunits (Groot Kormelink and Luyten, 1997 [PubMed 9009220]). Elliott et al. (1996) [PubMed 8906617] stated that the proposed structure for each subunit is a conserved N-terminal extracellular domain followed by 3 conserved transmembrane domains, a variable cytoplasmic loop, a fourth conserved transmembrane domain, and a short C-terminal extracellular region.

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CHST9