Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Alle Spezies anzeigen
Weitere Synonyme anzeigen
Wählen Sie die Spezies und Applikation aus
anti-Mouse (Murine) DDB2 Antikörper:
anti-Rat (Rattus) DDB2 Antikörper:
anti-Human DDB2 Antikörper:
Sie gelangen zu unserer vorgefilterten Suche.
Human Polyclonal DDB2 Primary Antibody für EIA, IP - ABIN117955
Luijsterburg, Goedhart, Moser, Kool, Geverts, Houtsmuller, Mullenders, Vermeulen, van Driel: Dynamic in vivo interaction of DDB2 E3 ubiquitin ligase with UV-damaged DNA is independent of damage-recognition protein XPC. in Journal of cell science 2007
Show all 7 Pubmed References
Results identified a missense mutation in damage-specific DNA binding protein 2 as a genetic risk factor for limbal squamous cell carcinoma in horses.
DDB2 plays a critical role in suppressing development of colon cancer at early stage by regulating Wnt (zeige WNT2 Antikörper) signaling. Mice genetically deficient in DDB2 exhibited increased susceptibility to colon tumor development in a manner associated with higher abundance of the Wnt receptor-expressing cells and greater activation of the downstream Wnt (zeige WNT2 Antikörper) pathway.
UVRAG (zeige UVRAG Antikörper) is a regulator of CRL4(DDB2)-mediated nucleotide excision repair and its expression levels may influence melanoma predisposition.
Results indicate a transcriptional regulatory pathway of DDB2 that is directly linked to the mechanisms that suppress metastasis of colon cancer.
Data indicate that poly(ADP-ribose) polymerase-1 (PARP-1 (zeige PARP1 Antikörper))collaborates with DNA-binding protein (zeige HSF4 Antikörper) 2 (DDB2) to increase the efficiency of the lesion recognition step of global genomic subpathway of NER (zeige NR1H2 Antikörper) (GG-NER (zeige NR1H2 Antikörper)).
the anti-proliferative and the pro-senescence pathways of DDB2 and p21 (zeige D4S234E Antikörper) are critical protection mechanisms against skin malignancies.
These results demonstrate direct activation of the human DDB2 gene by p53 (zeige TP53 Antikörper). The corresponding region in the mouse DDB2 gene shared significant sequence identity with the human gene but was deficient for p53 (zeige TP53 Antikörper) binding and transcriptional activation.
results demonstrate that DDB2 is well conserved between humans and mice and functions as a tumor suppressor, at least in part, by controlling p53 (zeige TP53 Antikörper)-mediated apoptosis after UV-irradiation
DDB2-deficient mice developed spontaneous malignant tumors at a high rate between the ages of 20 and 25 months.
DDB2 is involved in global repair in mouse epithelial cells.
Ddb2 heterozygosity can facilitate tumor development as a haploinsufficient tumor suppressor
DDB2 is modified by SUMOylation upon ultraviolet irradiation, and this post-translational modification plays an important role in the initial recognition and processing of ultraviolet irradiation-induced DNA damage occurring within the context of chromatin.
Results show that DDB2 is critical for chromatin association of XRCC5 (zeige XRCC5 Antikörper)/6 in the absence of DNA damage and provide evidence that XRCC5 (zeige XRCC5 Antikörper)/6 are functional partners of DDB2 in its transcriptional stimulatory activity.
High DDB2 expression is associated with increased radioresistance of non-small cell lung cancer.
data revealed that DDB2 is involved in early events occurring during metastatic progression of breast cancer cells and will contribute to define this protein as a new marker of metastatic progression in this type of cancer.
DDB2 polymorphisms are associated with gastric cancer and atrophic gastritis risks.
the release of NER (zeige NR1H2 Antikörper) components such as DNA damage binding protein 2 (DDB2) and Xeroderma Pigmentosum complementation group C (zeige XPC Antikörper) protein (XPC (zeige XPC Antikörper)) following oxidative stress might putatively involve their apoptotic role rather than DNA repair function.
PKM2 (zeige PKM2 Antikörper) interacts with DDB2 and reduces cell survival upon UV irradiation.
DDB2 can bind to the promoter region of NEDD4L (zeige NEDD4L Antikörper) and recruit enhancer of zeste homolog 2 (zeige EZH2 Antikörper) histone methyltransferase to repress NEDD4L (zeige NEDD4L Antikörper) transcription by enhancing histone H3 (zeige HIST3H3 Antikörper) lysine 27 trimethylation at the NEDD4L (zeige NEDD4L Antikörper) promoter.
data demonstrated that the DDB2 IRES activity was promoted during stress conditions. These results reveal a novel mechanism contributing to DDB2 expression
This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities.
damage-specific DNA binding protein 2 (48kD)
, damage-specific DNA binding protein 2, 48kDa
, DNA damage-binding protein 2
, Damage-specific DNA-binding protein 2
, DNA damage-binding protein 2-like
, damage-specific DNA-binding protein 2
, DDB p48 subunit
, UV-DDB 2
, UV-damaged DNA-binding protein 2
, xeroderma pigmentosum group E protein