RPMI 1640 Medium

RPMI 1640 medium
RPMI 1640 Medium

RPMI 1640 medium

500 mL
Catalog # 36750
34 USD

Overview

RPMI 1640 Medium is useful for a wide variety of cell culture applications. Selection of a suitable nutrient medium is dependent on cell type, culture conditions, and degree of chemical definition required for the cell culture application.
Subtype
Basal Media
Cell Type
Other
Species
Human, Mouse, Rat, Non-Human Primate, Other
Application
Cell Culture

Related Products

Scientific Resources

Product Documentation

Document Type Product Name Catalog # Lot # Language
Document Type
Product Information Sheet
Product Name
RPMI 1640 Medium
Catalog #
36750
Lot #
All
Language
English
Document Type
Safety Data Sheet 1
Product Name
RPMI 1640 Medium
Catalog #
36750
Lot #
All
Language
English
Document Type
Safety Data Sheet 2
Product Name
RPMI 1640 Medium
Catalog #
36750
Lot #
All
Language
English

Data and Publications

Publications (1)

Journal of immunology (Baltimore, Md. : 1950) 2006 JUL A role for DNA hypomethylation and histone acetylation in maintaining allele-specific expression of mouse NKG2A in developing and mature NK cells. S. L. Rogers et al.

Abstract

The repertoire of receptors that is expressed by NK cells is critical for their ability to kill virally infected or transformed cells. However, the molecular mechanisms that determine whether and when NK receptor genes are transcribed during hemopoiesis remain unclear. In this study, we show that hypomethylation of a CpG-rich region in the mouse NKG2A gene is associated with transcription of NKG2A in ex vivo NK cells and NK cell lines. This observation was extended to various developmental stages of NK cells sorted from bone marrow, in which we demonstrate that the CpGs are methylated in the NKG2A-negative stages (hemopoietic stem cells, NK progenitors, and NKG2A-negative NK cells), and hypomethylated specifically in the NKG2A-positive NK cells. Furthermore, we provide evidence that DNA methylation is important in maintaining the allele-specific expression of NKG2A. Finally, we show that acetylated histones are associated with the CpG-rich region in NKG2A positive, but not negative, cell lines, and that treatment with the histone deacetylase inhibitor trichostatin A alone is sufficient to induce NKG2A expression. Treatment with the methyltransferase inhibitor 5-azacytidine only is insufficient to induce transcription, but cotreatment with both drugs resulted in a significantly greater induction, suggesting a cooperative role for DNA methylation and histone acetylation status in regulating gene expression. These results enhance our understanding of the formation and maintenance of NK receptor repertoires in developing and mature NK cells.
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