RAD50 Anticorps
(RAD50 Homolog (S. Cerevisiae) (RAD50))
Choisissez l’un des 103 anticorps RAD50 de notre liste de produits basés sur 1 publication et 45 images de validation.
Découvrez des anticorps RAD50 fiables issus d’une large sélection de fabricants renommés. Notre portefeuille permet une détection précise de RAD50 dans plusieurs espèces, y compris Human, Mouse, Rat, Cow, Rabbit, Dog, Horse, Guinea Pig, Monkey, Bat, Chicken, Hamster, Saccharomyces cerevisiae, Zebrafish (Danio rerio), et prend en charge diverses applications de recherche telles que WB, IHC, ELISA, IF, FACS.
Trouvez rapidement l’anticorps adapté grâce à nos outils de recherche, de filtrage et de comparaison. Chaque page produit fournit des données de validation détaillées, des références bibliographiques et des retours d’utilisateurs. Contrairement aux ressources dédiées uniquement à la comparaison, vous pouvez acheter directement les anticorps sur notre site. Choisissez parmi des anticorps polyclonaux, monoclonaux ou recombinants RAD50, issus de différents hôtes tels que Rabbit, Mouse. Parcourez nos produits ci-dessous et commandez directement pour soutenir vos recherches en toute confiance.
Les noms alternatifs de RAD50 sont RAD50, Rad50, rad50, rad50.L, LOC658288, LOC726642, rad-50.
Filtrer les résultats:
103 Résultats
RAD50
Reactivité: Humain, Rat
WB, IHC, ELISA, FACS
Hôte: Souris
Monoclonal
3D2G10
unconjugated
RAD50
Reactivité: Humain
WB, IHC, IP
Hôte: Lapin
Polyclonal
unconjugated
1 reference
RAD50
Reactivité: Humain
ELISA
Hôte: Souris
Monoclonal
5A8E5
unconjugated
KD Validated
RAD50
Reactivité: Humain
WB, FACS
Hôte: Lapin
Monoclonal
23GB4115
unconjugated
Recombinant Antibody
RAD50
Reactivité: Humain, Souris, Rat
WB, IHC, ELISA, IF, ICC, FACS
Hôte: Lapin
Polyclonal
unconjugated
RAD50
Reactivité: Humain, Souris
IHC
Hôte: Lapin
Polyclonal
unconjugated
RAD50
Reactivité: Humain
WB, IHC
Hôte: Lapin
Polyclonal
unconjugated
RAD50
Reactivité: Souris
WB
Hôte: Lapin
Polyclonal
unconjugated
RAD50
Reactivité: Souris
WB
Hôte: Lapin
Polyclonal
RB40014
unconjugated
1 image
RAD50
Reactivité: Humain, Souris, Rat
WB, IHC, ELISA, IF
Hôte: Lapin
Polyclonal
unconjugated
1 image
RAD50
Reactivité: Humain, Souris, Boeuf (Vache), Lapin, Chien
IHC, IF, IHC (p)
Hôte: Lapin
Polyclonal
unconjugated
1 image
RAD50
Reactivité: Humain, Souris, Rat
WB, IHC, IF, ICC
Hôte: Lapin
Polyclonal
unconjugated
1 image
RAD50
Reactivité: Humain
WB, IP
Hôte: Lapin
Polyclonal
unconjugated
1 image
RAD50
Reactivité: Humain
WB, IHC, ELISA
Hôte: Lapin
Polyclonal
unconjugated
1 image
RAD50
Reactivité: Humain
WB, FACS, IHC (p), IF (cc), IF (p), IHC (fro)
Hôte: Lapin
Polyclonal
unconjugated
1 image
RAD50
Reactivité: Humain
WB, IHC, ELISA
Hôte: Lapin
Polyclonal
unconjugated
RAD50
Reactivité: Humain, Souris, Rat, Boeuf (Vache), Lapin, Cheval
WB, IP, PLA
Hôte: Lapin
Polyclonal
unconjugated
RAD50
Reactivité: Humain, Boeuf (Vache), Lapin, Chien
WB, IHC, IP, IF, IHC (p)
Hôte: Lapin
Polyclonal
unconjugated
Dernières publications pour nos RAD50 Anticorps
: "Increased error-free DNA repair gene expression through reprogramming in human iPS cells." dans: Regenerative therapy, Vol. 11, pp. 101-105, (2019) (PubMed).
: "NBS1 is regulated by two kind of mechanisms: ATM-dependent complex formation with MRE11 and RAD50, and cell cycle-dependent degradation of protein." dans: Journal of radiation research, Vol. 58, Issue 4, pp. 487-494, (2018) (PubMed).
: "Impaired DNA double-strand break repair contributes to the age-associated rise of genomic instability in humans." dans: Cell death and differentiation, Vol. 23, Issue 11, pp. 1765-1777, (2017) (PubMed).
: "The transcription factor GATA3 is required for homologous recombination repair by regulating CtIP expression." dans: Oncogene, Vol. 36, Issue 36, pp. 5168-5176, (2017) (PubMed).
: "HIF-1α-PDK1 axis-induced active glycolysis plays an essential role in macrophage migratory capacity." dans: Nature communications, Vol. 7, pp. 11635, (2016) (PubMed).
: "Targeting Rad50 sensitizes human nasopharyngeal carcinoma cells to radiotherapy." dans: BMC cancer, Vol. 16, pp. 190, (2016) (PubMed).
: "Cancer initiating-cells are enriched in the CA9 positive fraction of primary cervix cancer xenografts." dans: Oncotarget, Vol. 8, Issue 1, pp. 1392-1404, (2016) (PubMed).
: "Replication fork integrity and intra-S phase checkpoint suppress gene amplification." dans: Nucleic acids research, Vol. 43, Issue 5, pp. 2678-90, (2015) (PubMed).
: "Nijmegen breakage syndrome detected by newborn screening for T cell receptor excision circles (TRECs)." dans: Journal of clinical immunology, Vol. 35, Issue 2, pp. 227-33, (2015) (PubMed).
: "Increased oxidative stress in AOA3 cells disturbs ATM-dependent DNA damage responses." dans: Mutation research. Genetic toxicology and environmental mutagenesis, Vol. 782, pp. 42-50, (2015) (PubMed).
: "NBS1 is regulated by two kind of mechanisms: ATM-dependent complex formation with MRE11 and RAD50, and cell cycle-dependent degradation of protein." dans: Journal of radiation research, Vol. 58, Issue 4, pp. 487-494, (2018) (PubMed).
: "Impaired DNA double-strand break repair contributes to the age-associated rise of genomic instability in humans." dans: Cell death and differentiation, Vol. 23, Issue 11, pp. 1765-1777, (2017) (PubMed).
: "The transcription factor GATA3 is required for homologous recombination repair by regulating CtIP expression." dans: Oncogene, Vol. 36, Issue 36, pp. 5168-5176, (2017) (PubMed).
: "HIF-1α-PDK1 axis-induced active glycolysis plays an essential role in macrophage migratory capacity." dans: Nature communications, Vol. 7, pp. 11635, (2016) (PubMed).
: "Targeting Rad50 sensitizes human nasopharyngeal carcinoma cells to radiotherapy." dans: BMC cancer, Vol. 16, pp. 190, (2016) (PubMed).
: "Cancer initiating-cells are enriched in the CA9 positive fraction of primary cervix cancer xenografts." dans: Oncotarget, Vol. 8, Issue 1, pp. 1392-1404, (2016) (PubMed).
: "Replication fork integrity and intra-S phase checkpoint suppress gene amplification." dans: Nucleic acids research, Vol. 43, Issue 5, pp. 2678-90, (2015) (PubMed).
: "Nijmegen breakage syndrome detected by newborn screening for T cell receptor excision circles (TRECs)." dans: Journal of clinical immunology, Vol. 35, Issue 2, pp. 227-33, (2015) (PubMed).
: "Increased oxidative stress in AOA3 cells disturbs ATM-dependent DNA damage responses." dans: Mutation research. Genetic toxicology and environmental mutagenesis, Vol. 782, pp. 42-50, (2015) (PubMed).
Pseudonymes pour RAD50 Anticorps
RAD50 double strand break repair protein (RAD50) AnticorpsRAD50 double strand break repair protein (Rad50) Anticorps
CG6339 gene product from transcript CG6339-RE (rad50) Anticorps
RAD50 homolog, double strand break repair protein L homeolog (rad50.L) Anticorps
rad50 (LOC658288) Anticorps
DNA repair protein RAD50 (LOC726642) Anticorps
RAD50 homolog, double strand break repair protein (rad50) Anticorps
DNA repair-recombination protein (RAD50) (RAD50) Anticorps
MRX complex DNA-binding subunit (RAD50) Anticorps
DNA repair protein Rad50 (rad50) Anticorps
RAD50 recombination protein (RAD50) Anticorps
Rad50 DNA repair/recombination protein (Rad50) Anticorps
DNA repair protein rad-50 (rad-50) Anticorps
6339 Anticorps
ATRAD50 Anticorps
CG6339 Anticorps
Dmel\\CG6339 Anticorps
Dmrad50 Anticorps
DNA REPAIR-RECOMBINATION PROTEIN Anticorps
F22D22.28 Anticorps
F22D22_28 Anticorps
hRad50 Anticorps
im:6906849 Anticorps
Mrell Anticorps
NBSLD Anticorps
RAD50 Anticorps
Rad50 Anticorps
Rad50l Anticorps
RAD502 Anticorps
si:ch211-79h18.3 Anticorps
SPAP4C9.01c Anticorps
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