详细说明
Purity
>95%, by SDS-PAGE with silver staining
Endotoxin Level
<0.10 EU per 1 μg of the protein by the LAL method.
Activity
Measured by its ability to induce IL-6 secretion by monocyte-derived dendritic cells. The ED 50 for this effect is 0.6-3 μg/mL
Source
E. coli-derived Pro2-Asp100
Accession #
N-terminal Sequence
AnalysisPro2
Predicted Molecular Mass
11 kDa
SDS-PAGE
20 kDa, reducing conditions
8187-HM |
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Formulation Lyophilized from a 0.2 μm filtered solution in PBS. | ||
Reconstitution Reconstitute at 500 μg/mL in PBS. | ||
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below. | ||
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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Background: HMGN1
High-mobility group nucleosome-binding protein 1 (HMGN1), also known as HMG-14, is a member of the family of non-histone chromosomal proteins that play important roles in chromatin remodeling (1, 2). HMGN1 contains an N-terminal domain that interacts with nucleosomes and a C-terminal domain that assists chromatin unfolding (2, 3). Human HMGN1 shares 80% amino acid sequence identity with mouse and rat HMGN1. Alternative RNA processing generates a long isoform with a 45 amino acid insertion following Met1 (4). The trafficking of HMGN1 between the nucleus and cytoplasm is regulated by its serine phosphorylation at multiple sites (5, 6). In the nucleus, HMGN1 preferentially associates with sites of chromatin remodeling and gene transcription, allowing it to modulate the expression of a wide variety of genes (7, 8). It contributes to DNA damage repair by directly associating with and activating the double strand break sensor PARP-1 (9). HMGN1 is additionally one of several alarmins, proteins that are normally intracellular but are released following tissue damage or necrosis (1). In this setting, HMGN1 promotes dendritic cell maturation, recruitment to sites of inflammation, and production of Th1 inflammatory cytokines (10). These pro-inflammatory activities are dependent on the direct association of HMGN1 with the TLR4-MD2 complex on dendritic cells (10, 11).
References:
Yanai, H. et al. (2012) Trends Immunol. 33:633.
Gerlitz, G. (2010) Biochim. Biophys. Acta 1799:80.
Landsman, D. et al. (1986) J. Biol. Chem. 261:16082.
Zougman, A. et al. (2008) Curr. Biol. 18:1760.
Louie, D.F. et al. (2000) Protein Sci. 9:170.
Pogna, E.A. et al. (2010) Biochim. Biophys. Acta 1799:93.
Cuddapah, S. et al. (2011) Mol. Cell. Biol. 31:700.
Kugler, J.E. et al. (2013) J. Biol. Chem. 288:16690.
Masaoka, A. et al. (2012) J. Biol. Chem. 287:27648.
Yang, D. et al. (2010) Biochim. Biophys. Acta 1799:157.
Yang, D. et al. (2012) J. Exp. Med. 209:157.
Long Name:
High Mobility Group Nucleosome Binding Domain 1
Entrez Gene IDs:
3150 (Human); 15312 (Mouse); 360704 (Rat)
Alternate Names:
FLJ31471; High mobility group nucleosome-binding domain-containing protein 1; high-mobility group (nonhistone chromosomal) protein 14; high-mobility group nucleosome binding 1; high-mobility group nucleosome binding domain 1; HMG14; HMG14FLJ27265; HMGN1; MGC104230; MGC117425; non-histone chromosomal protein HMG-14; nonhistone chromosomal protein HMG-14