Nigericin Na+ salt, K+ ionophore (ab120494)
Key features and details
- K+ ionophore
- CAS Number: 28643-80-3
- Purity: > 98%
- Soluble in ethanol to 100 mM
- Form / State: Solid
- Source: Streptomyces hygroscopicus
Overview
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Product name
Nigericin Na+ salt, K+ ionophore -
Description
K+ ionophore -
Biological description
K+ ionophore; exchanges K+ for H+ across most biological membranes. Stimulates mitochondrial ATPase activity, and exchanges H+ for K+>Rb+>Cs+>>Na+. Reported to inhibit Poliovirus and influenza virus replication.
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Purity
> 98% -
CAS Number
28643-80-3 -
Chemical structure
Properties
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Chemical name
Nigericin sodium salt -
Molecular weight
746.95 -
Molecular formula
C40H67NaO11 -
PubChem identifier
16760591 -
Storage instructions
Store at +4°C. Store under desiccating conditions. The product can be stored for up to 12 months. -
Solubility overview
Soluble in ethanol to 100 mM -
Handling
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Toxic, refer to SDS for further information.
Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
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SMILES
OC[C@]1(O)O[C@@H]([C@@H](C)C[C@H]1C)[C@H]2C[C@H](C)[C@@H](O2)[C@]3(C)CC[C@@H](O3)[C@]6(C)C[C@@H](C)[C@@]5(O[C@H](C[C@H]4CC[C@H](C)[C@@H](O4)[C@@H](C)C(=O)O[Na])C[C@@H](OC)[C@H]5C)O6 -
Source
Streptomyces hygroscopicus
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Research areas
Images
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Functional Studies - Nigericin Na+ salt, K+ ionophore (ab120494)ab56889 staining mitofusin 2 in MEF1 cells treated with nigericin Na+ salt (ab120494), by ICC/IF. Decrease in mitofusin 2 expression correlates with increased concentration of nigericin Na+ salt, as described in literature.
The cells were incubated at 37°C for 3h in media containing different concentrations of ab120494 (nigericin Na+ salt) in DMSO, fixed with 100% methanol for 5 minutes at -20°C and blocked with PBS containing 10% goat serum, 0.3 M glycine, 1% BSA and 0.1% tween for 2h at room temperature. Staining of the treated cells with ab56889 (10 µg/ml) was performed overnight at 4°C in PBS containing 1% BSA and 0.1% tween. A DyLight 488 goat anti-mouse polyclonal antibody (ab96879) at 1/250 dilution was used as the secondary antibody. Nuclei were counterstained with DAPI and are shown in blue.
