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#18761 Anti-Human Sir2/SIRT1 Rabbit IgG Affinity Purify
- Intended Use:
- Research reagents
- Application:
- WB, IP, IHC
- Package Size1:
- 100 μg
- Package Size2:
- 10 μg
- Note on Application Abbreviations
- WB:Western Blotting
- IP:Immunoprecipitation
- IHC:Immunohistochemistry
※ The product indicated as "Research reagents" in the column Intended Use cannot be used
for diagnostic nor any medical purpose.
※ The datasheet listed on this page is sample only. Please refer to the datasheet
enclosed in the product purchased before use.
Product Overview
Product Overview
Product Code | 18761 |
---|---|
Product Name | Anti-Human Sir2/SIRT1 Rabbit IgG Affinity Purify |
Intended Use | Research reagents |
Application | WB, IP, IHC |
Species | Human |
Immunizing antigen | Synthetic peptides of the part of C-terminal of human Sir2/SIRT1(LEDEPDVPERAGG) |
Purification Method | Purified with antigen peptides |
Specificity | Confirmed by western blotting |
Package Form | Lyophilized product from PBS containing 1 % BSA and 0.05 % NaN3 |
Storage Condition | 2 - 8℃ |
Poisonous and Deleterious Substances | Applicable |
Cartagena | Not Applicable |
Package Size 1 | 100 μg |
Package Size 2 | 10 μg |
Remarks1 | The commercial use of products without our permission is prohibited. Please make sure to contact us and obtain permission. |
Product Description
Product Description
Imai et al. have found that S. cerevisiae Sir2p and its higher eukaryotic orthologs are novel nicotinamide adenine dinucleotide (NAD)-dependent histone/protein deacetylases. Sir2 proteins promote longevity in yeast and in C. elegans by silencing rDNA and regulating the insulin/IGF-1 signaling pathway, respectively. The enzymatic activities and functions of Sir2 proteins are highly conserved in evolution. In 2001, Vaziri, H. et al. have found that mammalian Sir2 negatively regulates the p53 function by physically interacting with and deacetylating the protein. This aspect of Sir2 function may connect various cellular damages, such as oxidative stress, to aging and carcinogenesis.
References
References
Note: Retrieve by PMID number in displayed by abstract: http://www.ncbi.nlm.nih.gov