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Key Documents

C0563

Sigma-Aldrich

Cardiolipin sodium salt from bovine heart

≥97% (TLC), lyophilized powder

Synonyme(s) :

Diphosphatidylglycerol

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About This Item

Numéro MDL:
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Source biologique

bovine heart

Niveau de qualité

Pureté

≥97% (TLC)

Forme

lyophilized powder

Type de lipide

phosphoglycerides

Conditions d'expédition

ambient

Température de stockage

−20°C

Description générale

Cardiolipin is localized in the inner membrane of mitochondria. It contains 18 carbon atoms, 3-phosphatidyl groups connected via a glycerol bridge. Cardiolipin is an important component of ATP synthase enzyme.

Application

Cardiolipin sodium salt from bovine heart has been used:
  • as a phospholipid standard in thin layer chromatography for the quantification of total mitochondrial lipids of Neurospora crassa(89)
  • as an internal standard in reverse phase high performance liquid chromatography (RP-HPLC) for quantification of bacterial lipid extracts(90)
  • as an antigen to evaluate IgM reaction in systemic lupus erythematosus (SLE) patients(91)

Actions biochimiques/physiologiques

Cardiolipin is a mitochondrial phospholipid that is found in mammalian tissues in low concentrations. It is often a membrane component. Inhibits cell attachment of fibronectin, vitronectin and Type I collagen.

Conditionnement

packaged under argon

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


Certificats d'analyse (COA)

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Analysis of mutations in Neurospora crassa ERMES components reveals specific functions related to beta-barrel protein assembly and maintenance of mitochondrial morphology
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PLoS ONE, 8(8), e71837-e71837 (2013)
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Acta pharmacologica Sinica, 39(6), 1012-1021 (2017-12-22)
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Antimicrobial resistance is a major threat the world is currently facing. Development of new antibiotics and the assessment of their toxicity represent important challenges. Current methods for addressing antibiotic toxicity rely on measuring mitochondrial damage using ATP and/or membrane potential
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Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 822(1-2), 40-53 (2005)
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