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06-172

Sigma-Aldrich

Anti-Na+/K+ ATPase α-3 Antibody

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702

biological source

rabbit

antibody form

purified antibody

clone

polyclonal

purified by

using Protein A

species reactivity

rat

manufacturer/tradename

Upstate®

technique(s)

immunohistochemistry: suitable
western blot: suitable

isotype

IgG

NCBI accession no.

UniProt accession no.

Specificity

Na+/K+ ATPase α-3

Immunogen

Fusion protein derived the alpha 3 subunit containing residues 320-514

Application

Anti-Na+/K+ ATPase α-3 Antibody detects level of Na+/K+ ATPase α-3 & has been published & validated for use in IH & WB.
Research Category
Neuroscience
Research Sub Category
Ion Channels & Transporters

Quality

routinely evaluated by immunoblot on brain microsomal preparations

Target description

112kDa

Physical form

0.1M Tris-HCl, pH 7.2, containing 0.02% sodium azide
Format: Purified

Storage and Stability

2 years at -20°C

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial

Regulatory Information

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D Romanovsky et al.
Neuroscience, 310, 342-353 (2015-09-20)
Ambulatory instability and falls are a major source of morbidity in the elderly. Age-related loss of tendon reflexes is a major contributing factor to this morbidity, and deterioration of the afferent limb of the stretch reflex is a potential contributing
Namrata Madan et al.
American journal of physiology. Cell physiology, 312(3), C222-C232 (2016-12-03)
The Na/K-ATPase α1 polypeptide supports both ion-pumping and signaling functions. The Na/K-ATPase α3 polypeptide differs from α1 in both its primary structure and its tissue distribution. The expression of α3 seems particularly important in neurons, and recent clinical evidence supports
Toke Jost Isaksen et al.
PLoS genetics, 13(5), e1006763-e1006763 (2017-05-05)
Mutations in the neuron-specific α3 isoform of the Na+/K+-ATPase are found in patients suffering from Rapid onset Dystonia Parkinsonism and Alternating Hemiplegia of Childhood, two closely related movement disorders. We show that mice harboring a heterozygous hot spot disease mutation
Steven J Clapcote et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(33), 14085-14090 (2009-08-12)
In a mouse mutagenesis screen, we isolated a mutant, Myshkin (Myk), with autosomal dominant complex partial and secondarily generalized seizures, a greatly reduced threshold for hippocampal seizures in vitro, posttetanic hyperexcitability of the CA3-CA1 hippocampal pathway, and neuronal degeneration in
Thomas Hellesøe Holm et al.
Scientific reports, 6, 31972-31972 (2016-08-24)
The Na(+)/K(+)-ATPases maintain Na(+) and K(+) electrochemical gradients across the plasma membrane, a prerequisite for electrical excitability and secondary transport in neurons. Autosomal dominant mutations in the human ATP1A3 gene encoding the neuron-specific Na(+)/K(+)-ATPase α3 isoform cause different neurological diseases

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