WB result of Phospho-4E-BP1 (Thr37/46) Recombinant Rabbit mAb
Blocking/Diluting buffer and concentration: 5% NFDM/TBST
Primary antibody: Phospho-4E-BP1 (Thr37/46) Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: MCF7 serum starved overnight, then amino acids starved for 1 hour whole cell lysate 6 µg
Lane 2: MCF7 serum starved overnight, then amino acids starved for 1 hour, followed by adding back amino acids for 1 hour and treating with 100 nM insulin for 30 minutes whole cell lysate 6 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 13 kDa
Observed MW: 15-20 kDa
Product Details
Product Details
Product Specification
| Host | Rabbit |
| Antigen | Phospho-4E-BP1 (Thr37/46) |
| Synonyms | Eukaryotic translation initiation factor 4E-binding protein 1; eIF4E-binding protein 1; Phosphorylated heat- and acid-stable protein regulated by insulin 1 (PHAS-I); EIF4EBP1 |
| Immunogen | Synthetic Peptide |
| Location | Cytoplasm, Nucleus |
| Accession | Q13541 |
| Clone Number | S-744-46 |
| Antibody Type | Recombinant mAb |
| Isotype | IgG |
| Application | WB |
| Reactivity | Hu, Ms, Rt |
| Purification | Protein A |
| Concentration | 0.5 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
| Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
| application | dilution | species |
| WB | 1:1000 | Hu, Ms, Rt |
Background
Phospho-4E-BP1 (Thr37/46) refers to the specific modified form of eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1) that has been phosphorylated at its threonine 37 and threonine 46 sites (Thr37/Thr46). 4E-BP1 is a key downstream effector protein of the mTORC1 signaling pathway, and its normal function is to act as a translation repressor: when in a hypophosphorylated state, it tightly binds to eukaryotic translation initiation factor 4E (eIF4E), preventing eIF4E from forming the initiation complex with eIF4G, thereby inhibiting the initiation of cap-dependent translation. However, when cells receive pro-growth signals such as growth factors, nutrients, or energy, the mTORC1 pathway is activated and preferentially catalyzes the phosphorylation of the Thr37 and Thr46 sites on the 4E-BP1 protein. This step is a foundational event for the "hyperphosphorylation" of 4E-BP1; it triggers a cascade of conformational changes in the protein, ultimately causing its dissociation from eIF4E. This release of eIF4E allows for the initiation of ribosome recruitment and protein synthesis. Therefore, detecting the level of Phospho-4E-BP1 (Thr37/46) serves as a highly sensitive and reliable molecular marker for gauging mTORC1 pathway activity. It is widely used as a key indicator in cancer research, metabolic diseases, and the study of cellular growth regulation to assess a cell's translational potential and proliferative status.
Picture
Picture
Western Blot
WB result of Phospho-4E-BP1 (Thr37/46) Recombinant Rabbit mAb
Blocking/Diluting buffer and concentration: 5% NFDM/TBST
Primary antibody: Phospho-4E-BP1 (Thr37/46) Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: Neuro-2a whole cell lysate 20 µg
Lane 2: C2C12 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 13 kDa
Observed MW: 15-20 kDa
WB result of Phospho-4E-BP1 (Thr37/46) Recombinant Rabbit mAb
Blocking/Diluting buffer and concentration: 5% NFDM/TBST
Primary antibody: Phospho-4E-BP1 (Thr37/46) Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: PC-12 whole cell lysate 20 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 13 kDa
Observed MW: 15-20 kDa
