SCC652
GLUTag Mouse Colonic Endocrine Cell Line

Synonyme(s) :
GLUTag, GLUTag cells, Murine GLUTag cells
About This Item
Produits recommandés
Source biologique
mouse
Niveau de qualité
Conditionnement
vial of ≥1 x 10^6 vial (viable cells per vial)
Fabricant/nom de marque
Millipore
Technique(s)
cell culture | mammalian: suitable
Conditions d'expédition
liquid nitrogen
Température de stockage
−196°C
Application
- Each vial contains > 1X106 viable cells.
- Cells are tested negative for infectious diseases by a Mouse Essential CLEAR Panel by Charles River Animal Diagnostic Services.
- Cells are verified to be of mouse origin and negative for interspecies contamination from human, rat, Chinese hamster, Golden Syrian hamster, and nonhuman primate (NHP) as assessed by a Contamination Clear panel by Charles River Animal Diagnostic Services
- Cells are negative for mycoplasma contamination.
Caractéristiques et avantages
Description de la cible
The GLUTag cell line is an effective intestinal endocrine L-cell model derived from colonic tumors of transgenic mice. This cell line secretes a variety of pro-glucagon derived peptides (PGDPs) such as GLI, IRG, and GLP-1.1 GLUTag cells are among one of the most widely used cell models to understand GLP-1 secretion. GLUTag cells are capable of activating GLP-1 secretion in vivo and have a phenotype that closely mirrors non-immortalized intestinal L-cells with some slight genetic differences. The immunoreactive profile of GLUTag cells also suggests L-cell lineage by being positively immunoreactive to GLP-1 and cholecystokinin, but negative for a large variety of other hormones such as calcitonin, insulin, and gastrin.
Although the GLUTag cell line has murine origins, they have been shown to have a relevant response mechanism that essentially mirrors the GLP-1 secretion response in humans. This means that testing potential therapeutic agents using GLUTag cells has been shown to still have a strong relevance to a human model. The ease-of-use of GLUTag cells becomes quite invaluable when compared to the difficulties of using primary human L-cells.
Source
Derived from an endocrine carcinoma in a mouse expressing SV40 Large T antigen. Fragments of the tumors were subcutaneously propagated in nude mice and individual cells from one of the tumors was isolated and single-cell cloned.
References
1. Drucker DJ, Jin T, Sylvia L, Young TA, Brubaker PL. 1994. Activation of proglucagon gene transcription by protein kinase-A in a novel mouse enteroendocrine cell line. Molecular Endocrinology. 8(12):1646–1655.
2. Kuhre RE, Wewer Albrechtsen NJ, Deacon CF, Balk-Møller E, Rehfeld JF, Reimann F, Gribble FM, Holst JJ. 2016. Peptide production and secretion in GLUTag, NCI-H716, and STC-1 cells: a comparison to native L-cells. Journal of Molecular Endocrinology. 56(3):201–211.
Stockage et stabilité
Autres remarques
Clause de non-responsabilité
Code de la classe de stockage
12 - Non Combustible Liquids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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