| Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human |
| Applications: | WB, IHC-P |
| Clonality: | Monoclonal |
| Clone number: | PS01-08 |
| Form: | Liquid |
| Storage condition: | Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term. |
| Storage buffer: | PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
| Concentration: | 1ug/ul |
| Purification: | Protein A affinity purified. |
| Molecular weight: | Predicted band size: 175 kDa |
| Isotype: | IgG |
| Immunogen: | Synthetic peptide corresponding to Human eIF4G1 (phospho S1108). |
| Positive control: | A431 cell lysate, SK-Br-3 cell lysate, MCF-7 cell lysate, human ovary cancer tissue. |
| Subcellular location: | Cytosol. Nucleus. |
| Recommended Dilutions:
WB IHC-P |
1:1,000 1:1,000 |
| Uniprot #: | SwissProt: Q04637 Human |
| Alternative names: | DKFZp686A1451 eIF 4 gamma 1 eIF 4G 1 eIF 4G1 eIF-4-gamma 1 eIF-4G 1 eIF-4G1 EIF4 gamma EIF4F EIF4G EIF4G1 EIF4GI Eukaryotic translation initiation factor 4 gamma 1 IF4G1_HUMAN p220 |
|
Fig1:
Western blot analysis of Phospho-eIF4G (S1108) on different lysates with Rabbit anti-Phospho-eIF4G (S1108) antibody (HA721276) at 1/1,000 dilution. Lane 1: A431 cell lysate Lane 2: SK-Br-3 cell lysate Lane 3: MCF-7 cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 175 kDa Observed band size: 250 kDa Exposure time: 2 minutes; 6% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721276) at 1/1,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature. |
|
Fig2:
Immunohistochemical analysis of paraffin-embedded human ovary cancer tissue untreated / treated with λpp with Rabbit anti-Phospho-eIF4G (S1108) antibody (HA721276) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721276) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX. |