The Phospho-eIF4EBP1-T37/T46 Monoclonal Antibody (CABP1381) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody, produced through monoclonal antibody technology, specifically targets the phosphorylated forms of EIF4EBP1 at threonine 37 and threonine 46 residues. It is highly reactive with human samples and has been validated for use in Western blot applications, allowing for precise detection and quantification of phosphorylated EIF4EBP1 in various cell types. This antibody is an essential tool for researchers interested in investigating the role of EIF4EBP1 in cell signaling pathways, particularly in cancer research and translational medicine.
This antibody is validated for use in WB, ELISA applications and has demonstrated reactivity against Human, Rat samples.
Product Name:
Phospho-eIF4EBP1-T37/T46 Monoclonal Antibody
SKU:
CABP1381
Size:
20μL, 100μL
Reactivity:
Human, Rat
Clone Number:
ARC56491
Conjugate:
Unconjugated
Immunogen:
Synthetic peptide. This information is considered to be commercially sensitive.
Tested Applications:
WBELISA
Recommended Dilution:
WB
1:1000 - 1:8000
ELISA
Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
This gene encodes one member of a family of translation repressor proteins. The protein directly interacts with eukaryotic translation initiation factor 4E (eIF4E), which is a limiting component of the multisubunit complex that recruits 40S ribosomal subunits to the 5' end of mRNAs. Interaction of this protein with eIF4E inhibits complex assembly and represses translation. This protein is phosphorylated in response to various signals including UV irradiation and insulin signaling, resulting in its dissociation from eIF4E and activation of mRNA translation.
Purification Method
Affinity purification
Gene ID
1978
Buffer Information
Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.09% Sodium azide,0.05% BSA,50% glycerol,pH7.3.
Western blot analysis of lysates from C6 cells using Phospho-eIF4EBP1-T37/T46 Rabbit mAb (CABP1381) at 1:7000 dilution incubated overnight at 4℃. C6 cells were treated with IGF-1 (100 ng/mL) at 37℃ for 30 minutes after serum-starvation overnight Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 30 μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 180s.
Western blot analysis of lysates from HeLa cells using Phospho-eIF4EBP1-T37/T46 Rabbit mAb (CABP1381) at 1:1000 dilution incubated overnight at 4℃. HeLa cells were treated with insiulin (100 nM) at 37℃ for 30 minutes. Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution. Lysates/proteins: 30 μg per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (AbGn00020). Exposure time: 90s.
