Recombinant Human ING2 protein (denatured)
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Recombinant Human ING2 protein (denatured) is a Human Full Length protein, in the 1 to 280 aa range, expressed in Escherichia coli, with >85%, suitable for SDS-PAGE.
View Alternative Names
ING1L, ING2, Inhibitor of growth protein 2, Inhibitor of growth 1-like protein, p32, p33ING2, ING1Lp
- SDS-PAGE
Unknown
SDS-PAGE - Recombinant Human ING2 protein (denatured) (AB171499)
15% SDS-PAGE analysis of ab171499 (3μg).
Reactivity data
Sequence info
Properties and storage information
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ING2 functions as a tumor suppressor by controlling the transcription of genes involved in cell cycle regulation and apoptosis. It interacts with histone acetyltransferase (HAT) and histone deacetylase (HDAC) complexes contributing to chromatin remodeling. As part of the Sin3A-HDAC complex ING2 has the ability to repress transcription influencing the expression of genes important for maintaining cellular homeostasis and preventing oncogenesis.
Pathways
The ING2 protein actively participates in the p53 signaling pathway as well as the MAPK signaling pathway. Its interaction with p53 leads to the enhancement of p53-mediated transcriptional activation which promotes cell cycle arrest and apoptosis. ING2 also interacts with proteins like TP53 and EP300 modulating the cellular responses to stress signals and contributing to cell survival and repair mechanisms.
Specifications
Form
Liquid
Additional notes
ab171499 is purified by using anion-exchange chromatography (DEAE sepharose resin) and gel-filtration chromatography.
General info
Function
Seems to be involved in p53/TP53 activation and p53/TP53-dependent apoptotic pathways, probably by enhancing acetylation of p53/TP53. Component of a mSin3A-like corepressor complex, which is probably involved in deacetylation of nucleosomal histones. ING2 activity seems to be modulated by binding to phosphoinositides (PtdInsPs).
Sequence similarities
Belongs to the ING family.
Post-translational modifications
Sumoylation enhances its association with SIN3A and is required for binding to some target gene promoters, this is the case for TMEM71.
Subcellular localisation
Nucleus
Target data
Product promise
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