E2F1 Rabbit Monoclonal Antibody(C3142)
MSDS 
Key features and details
- Target:
- Source/Host:
- Reactivity:
- Clonality:
- Applications:
- Conjugation:
- Storage:
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Brand:
Product Details
WB | 1:500 - 1:1000 |
IHC | 1:50 - 1:100 |
IF/ICC | 1:50 - 1:100 |
IP | 1:10 - 1:50 |
Description | Rabbit monoclonal antibody to E2F1 |
Specificity | Recognizes endogenous levels of E2F1 protein. |
Antibody Type | Primary antibody |
Imnunogen | A synthetic peptide of human E2F1 |
Purification | The antibody was purified by immunogen affinity chromatography. |
Molecular Weight | Predicted: 47 kD; Observed: 70 kD |
Form/Buffer | Liquid in 50mM Tris-Glycine (pH 7.4), 0.15M NaCl, 50% Glycerol, 0.01% Sodium azide and 0.05% BSA. |
Alternative Names | RBBP3; Transcription factor E2F1; E2F-1; PBR3; Retinoblastoma-associated protein 1; RBAP-1; Retinoblastoma-binding protein 3; RBBP-3; pRB-binding protein E2F-1 |
Gene Symbol | E2F1 |
Entrez Gene | 1869(Human); 13555(Mouse) |
SwissProt | Q01094(Human); Q61501(Mouse); O09139(Rat) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.
Western blot analysis of E2F1 expression in Molt4 (A), C6 (B), NIH3T3 (C) whole cell lysates. (Predicted band size: 47 kD; Observed band size: 70 kD)
Immunohistochemical analysis of E2F1 staining in human tonsil formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Immunofluorescent analysis of E2F1 staining in HeLa cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AREX® Fluor 488 -conjugated secondary antibody (green) in PBS at room temperature in the dark.
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