Human ATPase, Na+/K+ transporting, alpha 3 polypeptide ELISA Kit | ATP1A3 elisa kit

Human Sodium/potassium-transporting ATPase subunit alpha-3, ATP1A3 ELISA Kit

Cat. Num. AAA9319264

• Gene Names: ATP1A3; RDP; AHC2; DYT12
• Reactivity: Human
• Synonyms: ATPase; Na+/K+ transporting; alpha 3 polypeptide; Human Sodium/potassium-transporting ATPase subunit alpha-3; ATP1A3 ELISA Kit; Human Sodium/potassium-transporting ATPase subunit alpha-3 (ATP1A3) ELISA kit; DYT12; MGC13276; RDP; Na+/K+ -ATPase alpha 3 subunit; Na+/K+ ATPase 3; sodium pump 3; sodium-potassium-ATPase; sodium/potassium-transporting ATPase alpha-3 chain; ATP1A3 elisa kit

• Reactivity: Human
• Specificity: No significant cross-reactivity or interference between this analyte and analogues is observed.

• Samples: Undiluted original Human body fluids, tissue homogenates, secretions or feces samples. This kit is NOT suitable for assaying non-biological sources of substances.
• Assay Type: Sandwich
• Detection Range: 0.625 ng/ml - 20 ng/ml.
• Sensitivity: 0.1 ng/ml.
• Intra-assay Precision: Intra-assay CV (%) is less than 15%.
• Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100].
• Preparation and Storage: Store all reagents at 2-8 degree C

Related Product Information for ATP1A3 elisa kit

Background/Introduction: This Quantitative Sandwich ELISA kit is only for in vitro research use only! This kit is intended to be used for determination the level of ATP1A3 (hereafter termed "analyte") in undiluted original Human body fluids, tissue homogenates, secretions or feces samples. This kit is NOT suitable for assaying non-biological sources of substances.

NCBI and Uniprot Product Information

• NCBI GI #: 371940938
• NCBI GeneID: 478
• NCBI Accession #: NP_001243142.1
• NCBI GenBank Nucleotide #: NM_001256213.1
• UniProt Accession #: P13637; Q16732; Q16735; Q969K5; B7Z2T0; B7Z401; F5H6J6
• Molecular Weight: 111,749 Da
• NCBI Official Full Name: sodium/potassium-transporting ATPase subunit alpha-3 isoform 2
• NCBI Official Synonym Full Names: ATPase, Na+/K+ transporting, alpha 3 polypeptide
• NCBI Official Symbol: ATP1A3
• NCBI Official Synonym Symbols: RDP; AHC2; DYT12
• NCBI Protein Information: sodium/potassium-transporting ATPase subunit alpha-3; Na+/K+ ATPase 3; sodium pump subunit alpha-3; Na(+)/K(+) ATPase alpha-3 subunit; Na(+)/K(+) ATPase alpha(III) subunit; sodium-potassium-ATPase, alpha 3 polypeptide; sodium-potassium ATPase catalytic subunit alpha-3; sodium/potassium-transporting ATPase alpha-3 chain
• UniProt Protein Name: Sodium/potassium-transporting ATPase subunit alpha-3
• Protein Family: Sodium/potassium-transporting ATPase
• UniProt Gene Name: ATP1A3
• UniProt Synonym Gene Names: Na(+)/K(+) ATPase alpha-3 subunit
• UniProt Entry Name: AT1A3_HUMAN

NCBI Description

The protein encoded by this gene 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 3 subunit. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]

Uniprot Description

ATP1A3: This is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. This action creates the electrochemical gradient of sodium and potassium ions, providing the energy for active transport of various nutrients. Defects in ATP1A3 are the cause of dystonia type 12 (DYT12); also known as rapid-onset dystonia parkinsonism (RDP). DYT12 is an autosomal dominant dystonia- parkinsonism disorder. Dystonia is defined by the presence of sustained involuntary muscle contractions, often leading to abnormal postures. DYT12 patients develop dystonia and parkinsonism between 15 and 45 years of age. The disease is characterized by an unusually rapid evolution of signs and symptoms. The sudden onset of symptoms over hours to a few weeks, often associated with physical or emotional stress, suggests a trigger initiating a nervous system insult resulting in permanent neurologic disability. Belongs to the cation transport ATPase (P-type) (TC 3.A.3) family. Type IIC subfamily.

Protein type: Transporter, ion channel; Endoplasmic reticulum; Membrane protein, integral; Transporter; Membrane protein, multi-pass; Hydrolase; EC 3.6.3.9

Chromosomal Location of Human Ortholog: 19q13.31

Cellular Component: Golgi apparatus; endoplasmic reticulum; axon; plasma membrane; integral to membrane; synapse; nucleus; sodium:potassium-exchanging ATPase complex; vesicle; myelin sheath

Molecular Function: metal ion binding; chaperone binding; sodium:potassium-exchanging ATPase activity; D1 dopamine receptor binding; ATP binding

Biological Process: response to drug; cellular sodium ion homeostasis; potassium ion import; metabolic process; adult locomotory behavior; ionotropic glutamate receptor signaling pathway; visual learning; cellular potassium ion homeostasis; transmembrane transport; memory

Disease: Dystonia 12; Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy, And Sensorineural Hearing Loss; Alternating Hemiplegia Of Childhood 2