Mouse Calcium Channel, Voltage Dependent, L-Type, Alpha 1D Subunit (CACNa1D) ELISA Kit (96T)

Mouse Calcium Channel, Voltage Dependent, L-Type, Alpha 1D Subunit (CACNa1D) ELISA Kit (96T)

Catalog #: TD4637
Availability: In Stock
¥669.00
Detection range: 0.312-20ng/mL    
Sensitivity: 0.113ng/mL    
Type: Traditional CACNα1D ELISA kit    
Synonyms: CACH3; CACN4; CACNL1A2; CCHL1A2; Cav1.3; Voltage-gated calcium channel subunit alpha Cav1.3; Calcium channel, L type, alpha-1 polypeptide, isoform 2
Species: Mouse
Sample type: tissue homogenates, cell lysates or other biological fluids.
Experimental method: Sandwich
Shelf life: 12 months
Gene ID: 12289
UniProt ID: Q99246
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

Enables enzyme binding activity and voltage-gated calcium channel activity involved in cardiac muscle cell action potential. Involved in positive regulation of adenylate cyclase activity. Acts upstream of or within several processes, including adult walking behavior; regulation of blood circulation; and secretion by cell. Located in several cellular components, including T-tubule; Z disc; and dendritic shaft. Part of caveolar macromolecular signaling complex and voltage-gated calcium channel complex. Is expressed in several structures, including central nervous system; eye; genitourinary system; gut; and heart. Used to study Timothy syndrome. Human ortholog(s) of this gene implicated in Brugada syndrome 3; Timothy syndrome; long QT syndrome 8; and neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures. Orthologous to human CACNA1C (calcium voltage-gated channel subunit alpha1 C).

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