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Nom du produit
Kit d′immunoprécipitation des protéines de liaison à l′ARN Magna RIP®, RNA Immunoprecipitation (RIP) Kit containing all necessary reagents to perform 12 individual RNA-binding protein immunoprecipitation (RIP) reactions using protein A/G magnetic beads.
manufacturer/tradename
Magna RIP®
Upstate®
technique(s)
RIP: suitable
immunoprecipitation (IP): suitable
shipped in
dry ice
Quality Level
Catégories apparentées
Physical form
Application
Épigénétique et fonction nucléaire
Disclaimer
General description
Caractéristiques et avantages :
- Billes magnétiques avec protéine A/G, optimisées pour se lier aux complexes immuns acide nucléique-protéine
- Inhibiteurs de RNAses et réactifs exempts de RNAses
- Témoins négatifs
Other Notes
Tampon de lavage pour RIP
Tampon de lyse pour RIP
EDTA 0,5 M
SDS à 10 %
Solution saline I
Solution saline II
Promoteur de précipitation
IgG normale de souris
IgG de lapin purifiée
Cocktail d'inhibiteurs de protéases 200X
Inhibiteur de RNases
Protéinase K (10 mg/ml)
Eau exempte de nucléases
Packaging
Preparation Note
Legal Information
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
Classe de stockage
10 - Combustible liquids
Certificats d'analyse (COA)
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Contenu apparenté
All eukaryotic organisms require tight regulation of gene expression for complex processes such as development, differentiation, cell specification, and responses to environmental stimuli. Many genes are regulated post-transcriptionally, in addition to transcriptional mechanisms of gene regulation. RNA-binding proteins (RBPs) are essential for post-transcriptional gene regulation, linking transcription and translation in many processes including transcription, splicing, export, rate of translation and turnover. In all of these events, RBPs coordinate regulation of the amount of protein produced from mRNA transcripts.
Cancer is a complex disease manifestation. At its core, it remains a disease of abnormal cellular proliferation and inappropriate gene expression. In the early days, carcinogenesis was viewed simply as resulting from a collection of genetic mutations that altered the gene expression of key oncogenic genes or tumor suppressor genes leading to uncontrolled growth and disease (Virani, S et al 2012). Today, however, research is showing that carcinogenesis results from the successive accumulation of heritable genetic and epigenetic changes. Moreover, the success in how we predict, treat and overcome cancer will likely involve not only understanding the consequences of direct genetic changes that can cause cancer, but also how the epigenetic and environmental changes cause cancer (Johnson C et al 2015; Waldmann T et al 2013). Epigenetics is the study of heritable gene expression as it relates to changes in DNA structure that are not tied to changes in DNA sequence but, instead, are tied to how the nucleic acid material is read or processed via the myriad of protein-protein, protein-nucleic acid, and nucleic acid-nucleic acid interactions that ultimately manifest themselves into a specific expression phenotype (Ngai SC et al 2012, Johnson C et al 2015). This review will discuss some of the principal aspects of epigenetic research and how they relate to our current understanding of carcinogenesis. Because epigenetics affects phenotype and changes in epigenetics are thought to be key to environmental adaptability and thus may in fact be reversed or manipulated, understanding the integration of experimental and epidemiologic science surrounding cancer and its many manifestations should lead to more effective cancer prognostics as well as treatments (Virani S et al 2012).
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 17-700 | 04053252010880 |
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