Product Name
Phospho-eIF4G (S1108) Recombinant Rabbit Monoclonal Antibody [PS01-08] - BSA and Azide free
Antibody Type
Recombinant Rabbit monoclonal Antibody
Immunogen
Synthetic peptide corresponding to Human eIF4G1 (phospho S1108).
Target Molecular Weight
Predicted band size: 175 kDa
Positive Control
A431 cell lysate, SK-Br-3 cell lysate, MCF-7 cell lysate, human ovary cancer tissue.
Storage Instructions
Store at 2-8℃. Avoid freeze.
Purification Method
Protein A affinity purified.
Function
Eukaryotic translation initiation factor 4 G (eIF4G) is a protein involved in eukaryotic translation initiation and is a component of the eIF4F cap-binding complex. Orthologs of eIF4G have been studied in multiple species, including humans, yeast, and wheat. However, eIF4G is exclusively found in domain Eukarya, and not in domains Bacteria or Archaea, which do not have capped mRNA. As such, eIF4G structure and function may vary between species, although the human eIF4G 1 has been the focus of extensive studies. Across species, eIF4G strongly associates with eIF4E, the protein that directly binds the mRNA cap. Together with the RNA helicase protein eIF4A, these form the eIF4F complex. Within the cell eIF4G is found primarily in the cytoplasm, usually bound to eIF4E; however, it is also found in the nucleus, where its function is unknown. It may have a role in nonsense-mediated decay. eIF4G has been implicated in breast cancer. It appears in increased levels in certain types of breast cancer and increases production of mRNAs that contain IRESs; these mRNAs produce hypoxia- and stress-related proteins that encourage blood vessel invasion (which is important for tumorigenesis).
Background References
1. Weiniu Gan; Michael La Celle & Robert E. Rhoads (1998). "Functional Characterization of the Internal Ribosome Entry Site of eIF4G mRNA*". The Journal of Biological Chemistry. 273 (9): 5006–5012.
2. Ivan B. Lomakin; Christopher U. T. Hellen & Tatyana V. Pestova (2000). "Physical Association of Eukaryotic Initiation Factor 4G (eIF4G) with eIF4A Strongly Enhances Binding of eIF4G to the Internal Ribosomal Entry Site of Encephalomyocarditis Virus and Is Required for Internal Initiation of Translation". Mol Cell Biol. 20 (16): 6019–6029.
Synonyms
DKFZp686A1451 antibody
eIF 4 gamma 1 antibody
eIF 4G 1 antibody
eIF 4G1 antibody
eIF-4-gamma 1 antibody
eIF-4G 1 antibody
eIF-4G1 antibody
EIF4 gamma antibody
EIF4F antibody
EIF4G antibody
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DKFZp686A1451 antibody
eIF 4 gamma 1 antibody
eIF 4G 1 antibody
eIF 4G1 antibody
eIF-4-gamma 1 antibody
eIF-4G 1 antibody
eIF-4G1 antibody
EIF4 gamma antibody
EIF4F antibody
EIF4G antibody
EIF4G1 antibody
EIF4GI antibody
Eukaryotic translation initiation factor 4 gamma 1 antibody
IF4G1_HUMAN antibody
p220 antibody
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This data was developed using HA721276, the same antibody clone in a different buffer formulation.
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.
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☑ Cell treatment (CT)
This data was developed using HA721276, the same antibody clone in a different buffer formulation.
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.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"