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目录号:A5884
特异性 | FANCD2 Rabbit Recombinant mAb detects endogenous levels of total FANCD2. |
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背景 | Fanconi anemia (FA) is a rare human genetic disease displaying various clinical symptoms such as severe bone marrow failure, an extremely high incidence of cancer, and many other congenital defects. Upon activation, FA group D2 protein (FANCD2) is monoubiquitinated at K561 and works in cooperation with other FA and non-FA proteins to repair DNA damage. FANCD2 can perform the signaling transduction role in ATM signaling. Specifically, the phosphorylation of FANCD2 at Ser222, initiated by ATM, contributes to arresting cells in the S phase of the cell cycle. In the early phases of the DNA damage response, FANCD2 plays a crucial role as a sensor as well as a messenger for the timely repair of damaged DNA. |
抗体应用 | WB, IF,ELISA,ELISA | ||||
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稀释比例 |
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反应性 | Human Mouse Rat | ||||
MW (kDa) | 166kDa | ||||
抗体类型 | |||||
储存液配方 | 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. | ||||
储存条件 (自收到货起) |
Store at –20°C. |
WB
Validated by Selleck
IF
Validated by Selleck