Accéder au contenu
Merck
Toutes les photos(1)

Key Documents

G1767

Sigma-Aldrich

Glycogen from mussel, Mytilus genus

for DNA precipitations

Synonyme(s) :

DNA and RNA precipitation

Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme


About This Item

Numéro CAS:
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352200
Nomenclature NACRES :
NA.52

Qualité

for molecular biology

Niveau de qualité

Forme

liquid

Conditionnement

vial of 1 mL

Concentration

19-22 mg/mL

Température de stockage

−20°C

InChI

1S/C24H42O21/c25-1-5-9(28)11(30)16(35)22(41-5)39-4-8-20(45-23-17(36)12(31)10(29)6(2-26)42-23)14(33)18(37)24(43-8)44-19-7(3-27)40-21(38)15(34)13(19)32/h5-38H,1-4H2/t5-,6-,7-,8-,9-,10-,11+,12+,13-,14-,15-,16-,17-,18-,19-,20-,21+,22+,23-,24-/m1/s1

Clé InChI

BYSGBSNPRWKUQH-UJDJLXLFSA-N

Vous recherchez des produits similaires ? Visite Guide de comparaison des produits

Description générale

Glycogen is a branched polymer of glucose synthesized by animal cells for energy storage and release. It is constructed of predominantly α1→4 glycosidic bonds with branches created through α1→6 glycosidic bonds.
Glycogen is a branched polymer of glucose that coprecipitates nucleic acids during isolation and purification.

Application

Glycogen from Mytilus genus (Blue mussel) has been used


  • as a coprecipitant in the isolation of RNA from hepatocytes and yeast cells.
  • as a reference standard in calibration curve generation to quantify hepatic glycogen content.
  • as a carrier molecule for DNA and RNA, replacing tRNA or sonicated DNA
  • for the precipitation of DNA in the presence of ammonium acetate and ethanol or isopropanol
  • for recovery of tRNA, yeast RNA, sonicated DNA and oligonucleotides as short as 8 base pairs

Actions biochimiques/physiologiques

Glycogen levels in Mytilus genus shows variation during seasonal changes. It is a crucial stored energy reserve for Mussels and is utilized during gametogenesis. Glycogen levels dictate the reproductive capacity and development of mussels larva. Glycogen aids in the coprecipitation of nucleic acids during isolation and purification.

Caractéristiques et avantages

  • product provided is 1 mL total volume
  • precipitates even small amounts of DNA and RNA present in dilute solutions
  • does not interfere with OD 260/280 readings

Principe

Glycogen is an inert carrier that traps nucleic acids. It forms a precipitate with DNA/RNA while being insoluble in ethanol solution. Due to the manufacturing process, there is low risk of contaminating nucleic acids in the glycogen. This product is tested for DNase, RNase, and NICKase, but not nucleic acids.

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)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

Déjà en possession de ce produit ?

Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Regulation of gluconeogenesis by Kruppel-like factor 15
Gray S, et al.
Cell Metabolism, 5(4), 305-312 (2007)
Energy storage and reproduction in mussels, Mytilus galloprovincialis: the influence of diet quality
Fearman JA, et al.
Journal of shellfish research., 28(2), 305-312 (2009)
Tri-methylation of histone H3 lysine 4 facilitates gene expression in ageing cells
Cruz C, et al.
eLife, 7, e34081-e34081 (2018)
Biomass composition of blue mussels, Mytilus edulis, is affected by living site and species of ingested microalgae
Pleissner D, et al.
ISRN zoology, 2012 (2012)
Mitchell B Rosen et al.
Toxicology, 308, 129-137 (2013-04-10)
While perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) have been studied at length, less is known about the biological activity of other perfluoroalkyl acids (PFAAs) detected in the environment. Using a transient transfection assay developed in COS-1 cells, our group

Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..

Contacter notre Service technique