Ruthenium Red
CAS No. 11103-72-3
Ruthenium Red( Ammoniated ruthenium oxychloride )
Catalog No. M23311 CAS No. 11103-72-3
Ruthenium Red is a polycationic dye widely used for electron microscopy (EM) of cells, tissues and vegetative bacteria.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | 32 | In Stock |
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| 200MG | 45 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameRuthenium Red
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NoteResearch use only, not for human use.
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Brief DescriptionRuthenium Red is a polycationic dye widely used for electron microscopy (EM) of cells, tissues and vegetative bacteria.
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DescriptionRuthenium Red is a polycationic dye widely used for electron microscopy (EM) of cells, tissues and vegetative bacteria. Ruthenium red strongly reacts with phospholipids and fatty acids and binds to acidic mucopolysaccharides. Ruthenium red is a L-type calcium current (ICa) blocker, blocks Ca2+ uptake and release, and voltage-sensitive Ca2+ channels.
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In Vitro——
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In Vivo——
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SynonymsAmmoniated ruthenium oxychloride
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorCalcium Channel
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Research Area——
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Indication——
Chemical Information
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CAS Number11103-72-3
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Formula Weight——
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Molecular Formula——
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Purity>98% (HPLC)
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SolubilityDMSO:10 mg/mL (Need ultrasonic);H2O:< 0.1 mg/mL (ultrasonic) (insoluble)
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SMILES——
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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TPC2-A1-P is a membrane-permeable two-pore channel 2 (TPC2) agonist that differentially activates two-pore channel 2 (TPC2) and mimics the activation of TPC2 with NAADP and PIP(2). TPC2-A1-P can be used to study neurodegenerative lysosomal storage diseases.
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TTA-A2
TTA-A2 is a selective T-type calcium channel antagonist as a potent anticonvulsant that the Cav3.1 isoform plays a prominent role in mediating.?
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TTA-Q6
TTA-Q6, a selective T-type Ca2+ channel antagonist, exhibits potential antitumor and immunomodulatory activities for treating neurological disorders by inhibiting the uptake of extracellular calcium ions by tumor cells, thereby inducing intracellular calcium deficiency and endoplasmic reticulum (ER) stress.
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