Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations
- Western blot [1]
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Validation data
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- Product number
- PAB9924 - Provider product page
- Provider
- Abnova Corporation
- Proper citation
- Abnova Corporation Cat#PAB9924, RRID:AB_1672163
- Product name
- ATR polyclonal antibody
- Antibody type
- Polyclonal
- Description
- Rabbit polyclonal antibody raised against synthetic peptide of ATR.
- Storage
- Store at 4°C. For long term storage store at -20°C.Aliquot to avoid repeated freezing and thawing.
Submitted references Che-1 phosphorylation by ATM/ATR and Chk2 kinases activates p53 transcription and the G2/M checkpoint.
RPA2 is a direct downstream target for ATR to regulate the S-phase checkpoint.
ATR-dependent phosphorylation and activation of ATM in response to UV treatment or replication fork stalling.
Bruno T, De Nicola F, Iezzi S, Lecis D, D'Angelo C, Di Padova M, Corbi N, Dimiziani L, Zannini L, Jekimovs C, Scarsella M, Porrello A, Chersi A, Crescenzi M, Leonetti C, Khanna KK, Soddu S, Floridi A, Passananti C, Delia D, Fanciulli M
Cancer cell 2006 Dec;10(6):473-86
Cancer cell 2006 Dec;10(6):473-86
RPA2 is a direct downstream target for ATR to regulate the S-phase checkpoint.
Olson E, Nievera CJ, Klimovich V, Fanning E, Wu X
The Journal of biological chemistry 2006 Dec 22;281(51):39517-33
The Journal of biological chemistry 2006 Dec 22;281(51):39517-33
ATR-dependent phosphorylation and activation of ATM in response to UV treatment or replication fork stalling.
Stiff T, Walker SA, Cerosaletti K, Goodarzi AA, Petermann E, Concannon P, O'Driscoll M, Jeggo PA
The EMBO journal 2006 Dec 13;25(24):5775-82
The EMBO journal 2006 Dec 13;25(24):5775-82
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Supportive validation
- Submitted by
- Abnova Corporation (provider)
- Main image
- Experimental details
- Western blot using ATR polyclonal antibody (Cat # PAB9924) in HeLa cell nuclear extract (Lane 1).Lane 2 shows negligible staining after pre-incubation of antibody with the immunizing peptide (50 ug peptide for 1 h at room temperature followed by centrifugation).A 4-8% gradient gel was used for separation.Goat serum was used at 5% for blocking.The arrowhead corresponds to 301 kDa ATR.The primary antibody was used at a 1 : 1,400 dilution.