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用途
sufficient for 100 fluorometric tests
检测方法
fluorometric
储存温度
−20°C
一般描述
SIRT6 or Sirtuin 6 proteins are a class of proteins that possess either histone deacetylase or mono-ribosyltransferase activity. SIRT6 is a nuclear sirtuin that has been associated with aging, cellular protection, sugar metabolism and certain types of cancer. Broad therapeutic applications are foreseen for SIRT6 inhibitors, including uses in diabetes, immune-mediated disorders, and cancer. Unlike other known protein deacetylases, which simply hydrolyze acetyl-lysine residues, the sirtuin-mediated deacetylation reaction hydrolyzes acetyl-lysine and NAD. This hydrolysis yields the deacetylated substrate, O-acetyl-ADP-ribose and nicotinamide, itself an inhibitor of sirtuin activity. Studies suggest that the human sirtuins may function as intracellular regulatory proteins with mono-ADP-ribosyltransferase activity.
特点和优势
Compatible with high-throughput handling systems.
适用性
Suitable for screening, characterizing and studying SIRT6 inhibitors
原理
In this Sirtuin 6 inhibitor screening kit, Sirtuin 6 deacetylates the substrate, followed by cleavage of the deacetylated substrate to release the fluorescent group, which is detected fluorometrically (λex = 400 nm/λem = 505 nm).
警示用语:
Danger
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Repr. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1
储存分类代码
10 - Combustible liquids
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Overexpression of sirtuin 6 suppresses inflammatory responses and bone destruction in mice with collagen-induced arthritis.
Arthritis and Rheumatism, 65, 1776-1785 (2013)
SIRT6 inhibitors with salicylate-like structure show immunosuppressive and chemosensitizing effects.
Bioorganic & Medicinal Chemistry, 25, 5849-5858 (2017)
Neural sirtuin 6 (Sirt6) ablation attenuates somatic growth and causes obesity.
Proceedings of the National Academy of Sciences of the USA, 107, 21790-21794 (2010)
Sirtuin 6 protects cardiomyocytes from hypertrophy in vitro via inhibition of NF-?B-dependent transcriptional activity.
British Journal of Pharmacology, 168, 117-128 (2013)
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