A3979
Anti-Na+/K+ ATPase (β2-subunit) antibody produced in rabbit
whole antiserum, liquid
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About This Item
MDL number:
UNSPSC Code:
12352203
biological source
rabbit
conjugate
unconjugated
antibody form
whole antiserum
antibody product type
primary antibodies
clone
polyclonal
form
liquid
species reactivity
rat
technique(s)
immunohistochemistry: 1:200
western blot: 1:1,000 using brain microsomal preparation
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
Gene Information
rat ... Atp1b2(24214)
General description
The Na+/K+ ATPase is an integral membrane enzyme that regulates ATP-dependent transport of Na+ and K+ across cell membranes. The Na+/K+ ATPase consists of a large, multipass, transmembrane catalytic α subunit, and an associated smaller β glycoprotein subunit. Studies indicate that there are three isoforms of the α subunit (α1, 2, and 3) and two isoforms of the β subunit (β1 and 2) encoded by two multigene families. Rabbit anti-Na+/K+ ATPase (β2-subunit) antibody is specific for the rat β2-subunit.
Immunogen
β2 subunit fusion protein containing residues 63-285, as deduced from cDNA. The β2 subunit exhibits virtual identity with the glial cell adhesion molecule AMOG.
Application
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Western Blotting (1 paper)
Western Blotting (1 paper)
Rabbit anti-Na+/K+ ATPase (β2-subunit) antibody can be used for western blot (1:1,000 using brain microsomal preparation) and immunohistochemistry (1:200) assays.
Physical form
The antibody is supplied as 200μL of whole antiserum
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 uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Y Sun et al.
The American journal of physiology, 262(6 Pt 1), C1491-C1499 (1992-06-11)
While Western blot analysis clearly revealed the presence of the alpha- and beta-subunits of Na(+)-K(+)-ATPase in a variety of rat tissues, beta was not readily detectable in liver. This observation was consistent with a previous report indicating that Na(+)-K(+)-ATPase immunoprecipitated
A Mobasheri et al.
Cell biology international, 21(4), 201-212 (1997-04-01)
We have used isoform-specific antibodies against the Na+, K(+)-ATPase alpha (alpha 1, alpha 2 and alpha 3) and beta (beta 1 and beta 2) subunit isoforms in order to establish their specific localization in isolated bovine articular chondrocytes. Immunoblotting confirmed
Lylia Nini et al.
BMC biochemistry, 8, 18-18 (2007-09-21)
Heterotrimeric guanine nucleotide-binding regulatory proteins (G proteins), composed of G alpha, G beta, and G gamma subunits, are positioned at the inner face of the plasma membrane and relay signals from activated G protein-coupled cell surface receptors to various signaling
Michał Biernacki et al.
Advances in medical sciences, 64(1), 15-23 (2018-09-23)
The effect of chronic administration of [3-(3-carbamoylphenyl)phenyl] N-cyclohexylcarbamate (URB597), inhibitor of fatty acid amide hydrolase (FAAH) that hydrolyzes anandamide, on cross-talk between endocannabinoid system, oxidative status and pro-inflammatory factors in the liver of spontaneously hypertensive rats (SHRs) was investigated. Experiments
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