RNF168 抗体
(Ring Finger Protein 168 (RNF168))
This gene encodes an E3 ubiquitin ligase protein that contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The protein is involved in DNA double-strand break (DSB) repair. Mutations in this gene result in Riddle syndrome. [provided by RefSeq, Sep 2011].
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RNF168
适用: 人, 小鼠, 大鼠, 犬, 豚鼠, 兔, Hamster, 猴
WB, IHC, IHC (p)
宿主: 兔
Polyclonal
unconjugated
2 images
Latest Publications for our RNF168 抗体
: "RNF168-mediated H2A neddylation antagonizes ubiquitylation of H2A and regulates DNA damage repair." in: Journal of cell science, Vol. 127, Issue Pt 10, pp. 2238-48, (2014) (PubMed).
: "miR-15a/miR-16 down-regulates BMI1, impacting Ub-H2A mediated DNA repair and breast cancer cell sensitivity to doxorubicin." in: Scientific reports, Vol. 7, Issue 1, pp. 4263 (PubMed).
: "miR-15a/miR-16 down-regulates BMI1, impacting Ub-H2A mediated DNA repair and breast cancer cell sensitivity to doxorubicin." in: Scientific reports, Vol. 7, Issue 1, pp. 4263 (PubMed).
Aliases for RNF168 抗体
ring finger protein 168 (Rnf168) 抗体ring finger protein 168, E3 ubiquitin protein ligase L homeolog (rnf168.L) 抗体
ring finger protein 168 (RNF168) 抗体
3110001H15Rik 抗体
hRNF168 抗体
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