Human ATPase, Na+/K+ Transporting Beta 1 Polypeptide (ATP1b1) ELISA Kit (96T)

Human ATPase, Na+/K+ Transporting Beta 1 Polypeptide (ATP1b1) ELISA Kit (96T)

Catalog #: TD3153
Availability: In Stock
¥649.00
Detection range: 0.156-10ng/mL    
Sensitivity: 0.066ng/mL    
Type: Traditional ATP1β1 ELISA kit    
Synonyms: ATP1B; Sodium/Potassium-Dependent ATPase Subunit beta-1
Species: Human
Sample type: serum, plasma, tissue homogenates or other biological fluids.
Experimental method: Sandwich
Shelf life: 12 months
Gene ID: 481
UniProt ID: P05026
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 protein encoded by this gene ATP1A2 belongs to the family of P-type cation transport ATPases, and to the subfamily of Na+/K+ -ATPases. Na+/K+ -ATPase is an integral membrane protein responsible for establishing and maintaining the electrochemical gradients of Na and K ions across the plasma membrane. These gradients are essential for osmoregulation, for sodium-coupled transport of a variety of organic and inorganic molecules, and for electrical excitability of nerve and muscle. This enzyme is composed of two subunits, a large catalytic subunit (alpha) and a smaller glycoprotein subunit (beta). The catalytic subunit of Na+/K+ -ATPase is encoded by multiple genes. This gene encodes an alpha 2 subunit. Mutations in this gene result in familial basilar or hemiplegic migraines, and in a rare syndrome known as alternating hemiplegia of childhood

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