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ImmunocytochemistryAntibody data
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- References [5]
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- Product number
- ABIN394233 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-RECQL2 (ARABIDOPSIS RECQ HELICASE L2), 3'-5' DNA Helicase/ ATP-Dependent Helicase/ Four-Way Junction Helicase/ Protein Binding (RECQL2) (AA 1322-1433) 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 1322-1433
- Isotype
- IgG
- Antibody clone number
- 3C11
- 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 Centrosome-related genes, genetic variation, and risk of breast cancer.
Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Variation within DNA repair pathway genes and risk of multiple sclerosis.
Lack of association of the WRN C1367T polymorphism with senile cataract in the Israeli population.
Identification of a coiled coil in werner syndrome protein that facilitates multimerization and promotes exonuclease processivity.
Olson JE, Wang X, Pankratz VS, Fredericksen ZS, Vachon CM, Vierkant RA, Cerhan JR, Couch FJ
Breast cancer research and treatment 2011 Jan;125(1):221-8
Breast cancer research and treatment 2011 Jan;125(1):221-8
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
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
Lack of association of the WRN C1367T polymorphism with senile cataract in the Israeli population.
Ehrenberg M, Dratviman-Storobinsky O, Avraham-Lubin BR, Goldenberg-Cohen N
Molecular vision 2010 Aug 28;16:1771-5
Molecular vision 2010 Aug 28;16:1771-5
Identification of a coiled coil in werner syndrome protein that facilitates multimerization and promotes exonuclease processivity.
Perry JJ, Asaithamby A, Barnebey A, Kiamanesch F, Chen DJ, Han S, Tainer JA, Yannone SM
The Journal of biological chemistry 2010 Aug 13;285(33):25699-707
The Journal of biological chemistry 2010 Aug 13;285(33):25699-707
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- Submitted by
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- Main image
- Experimental details
- WB
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- WB
Supportive validation
- Submitted by
- antibodies-online (provider)
- Main image
- Experimental details
- ELISA
