Recombinant full length human EIF2S1 was expressed in E. coli cells using a N-terminal His tag.
Catalog No. E23-54H
Catalog No. | Pack Size | Price (USD) | |
---|---|---|---|
E23-54H-20 | 20 ug | $215 | |
E23-54H-50 | 50 ug | $435 | |
E23-54H-BULK | BULK | Contact Us |
Overview:
EIF2S1, also known as eukaryotic translation initiation factor 2, subunit 1 alpha, is a 35kDa protein in which The translation initiation factor EIF2 catalyzes the first regulated step of protein synthesis initiation and promotes the binding of the initiator tRNA to 40S ribosomal subunits. Binding occurs as a ternary complex of methionyl-tRNA, EIF2, and GTP (1). The Ser51 in the mature human EIF2-alpha protein acts as the sole site of phosphorylation that leads to repression of protein synthesis. EIF2-alpha also plays an essential role in erythropoiesis (2).
Gene Aliases:
EIF-2; EIF-2A; EIF-2alpha; EIF2; EIF2A
Genbank Number:
References:
1. Ernst, H. et.al: Cloning and sequencing of complementary DNAs encoding the alpha-subunit of translational initiation factor eIF-2: characterization of the protein and its messenger RNA. J. Biol. Chem. 262: 1206-1212, 1987.
2. Pathak, V. K.et.al: Generation of a mutant form of protein synthesis initiation factor eIF-2 lacking the site of phosphorylation by eIF-2 kinases. Molec. Cell. Biol. 8: 993-995, 1988.
Purity:
Sample Purity Data. For specific information on a given lot, see related technical data sheet.
Storage, Stability and Shipping:
Store product at –70oC. For optimal storage, aliquot target into smaller quantities after centrifugation and store at recommended temperature. For most favorable performance, avoid repeated handling and multiple freeze/thaw cycles.
Molecular Weight:
~40 kDa
JB Bell et al., Differential Response of Glioma Stem Cells to Arsenic Trioxide Therapy is Regulated by MNK1 and mRNA Translation Mol Cancer Res October 2017 10.1158/1541-7786.MCR-17-0397
B Bell Jonathan et al., Differential Response of Glioma Stem Cells to Arsenic Trioxide Therapy is Regulated by MNK1 and mRNA Translation Mol Cancer res 10.1158/1541-7786.MCR-17-0397
Angiogenesis, Cellular Stress, Inflammation, Neurobiology, Ser/Thr Kinases
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