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Each lot of this antibody is quality control tested by Western blotting. Western blotting, suggested working dilution(s): Use 10 µl per 5 ml antibody dilution buffer for each mini-gel. It is recommended that the reagent be titrated for optimal performance for each application.
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Hela cell extract was resolved by electrophoresis, transferred to nitrocellulose and probed with polyclonal ant-eIF/p116 antibody. Proteins were visualized using a goat anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.
The eIF3/p116 polyclonal antibody recognizes human eIF3/p116 also known as eukaryotic translation initiation factor 3, subunit 9 eta 116 kD, EIF3 ETA, EIF3 P110, eIF3b, and PRT1. eIF3/p116 is a member of the eukaryotic translation initiation factor 3 family. eIF-3 is the largest of the eIFs and is composed of at least 12 different subunits; eIF3/p116 is one such subunit with an apparent molecular weight of 116 kD. eIF3/p116 is a ubiquitously expressed ribosome protein that binds to the 40s ribosome and promotes the binding of methionyl-tRNA and mRNA. eIF3/p116 has been shown to interact with other subunits of EIF-3, IL-2Rβ, and TRIP1 protein. The eIF3/p116 antibody has been shown to be useful for Western blotting.
Eukaryotic initiation factor-3 (eIF3) is the largest of the eIFs and is composed of at least 12 different subunits; eIF3/p116 is one such subunit with an apparent molecular weight of 116 kD.
Distribution:
Ribosome, ubiquitously expressed
Function:
Binds to the 40s ribosome and promotes the binding of methionyl-tRNA and mRNA.
Interaction:
EIF3S1, EIF3S4, EIF3S10, IL-2Rβ, and TRIP1
Antigen References:
1. Asano K, et al. 1997. J. Biol. Chem. 272:1101. 2. MethotN, et al. 1997. J. Biol. Chem. 272:1110.
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This data display is provided for general comparisons between formats. Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors. If you need assistance with selecting the best format contact our expert technical support team.
Purified anti-eIF3/p116
Hela cell extract was resolved by electrophoresis, transferred to nitrocellulose and probed with polyclonal ant-eIF/p116 antibody. Proteins were visualized using a goat anti-rabbit secondary conjugated to HRP and a chemiluminescence detection system.