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- Product number
- ABIN396279 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-X-Ray Repair Complementing Defective Repair in Chinese Hamster Cells 6 (XRCC6) (AA 1-610) antibody
- Antibody type
- Monoclonal
- Description
- This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
- Reactivity
- Human
- Host
- Mouse
- Epitope
- AA 1-610
- Isotype
- IgG
- Antibody clone number
- 4C2-1A6
- Vial size
- 100 μg
- Storage
- Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles
Submitted references Analysis of the polymorphisms in non-homologous DNA end joining (NHEJ) gene Ku70 and Ligase IV in sporadic breast cancer in women.
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk.
Ku70 corrupts DNA repair in the absence of the Fanconi anemia pathway.
Variation within DNA repair pathway genes and risk of multiple sclerosis.
Sobczuk A, Smolarz B, Romanowicz H, Zadrozny M, Baszczyński J, Westfal B, Pertyński T
Polish journal of pathology : official journal of the Polish Society of Pathologists 2010;61(1):27-31
Polish journal of pathology : official journal of the Polish Society of Pathologists 2010;61(1):27-31
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S, DREAM investigators.
Diabetes care 2010 Oct;33(10):2250-3
Diabetes care 2010 Oct;33(10):2250-3
Gamma-radiation sensitivity and polymorphisms in RAD51L1 modulate glioma risk.
Liu Y, Shete S, Wang LE, El-Zein R, Etzel CJ, Liang FW, Armstrong G, Tsavachidis S, Gilbert MR, Aldape KD, Xing J, Wu X, Wei Q, Bondy ML
Carcinogenesis 2010 Oct;31(10):1762-9
Carcinogenesis 2010 Oct;31(10):1762-9
Ku70 corrupts DNA repair in the absence of the Fanconi anemia pathway.
Pace P, Mosedale G, Hodskinson MR, Rosado IV, Sivasubramaniam M, Patel KJ
Science (New York, N.Y.) 2010 Jul 9;329(5988):219-23
Science (New York, N.Y.) 2010 Jul 9;329(5988):219-23
Variation within DNA repair pathway genes and risk of multiple sclerosis.
Briggs FB, Goldstein BA, McCauley JL, Zuvich RL, De Jager PL, Rioux JD, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Oksenberg JR, Sawcer SJ, Pericak-Vance MA, Haines JL, Barcellos LF, International Multiple Sclerosis Genetics Consortium.
American journal of epidemiology 2010 Jul 15;172(2):217-24
American journal of epidemiology 2010 Jul 15;172(2):217-24
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