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EIF2B1 encodes one of five subunits of eukaryotic translation initiation factor 2B (EIF2B), a GTP exchange factor for eukaryotic initiation factor 2 and an essential regulator for protein synthesis. Additionally we are shipping Eukaryotic Translation Initiation Factor 2B, Subunit 1 Alpha, 26kDa Antibodies (36) and many more products for this protein.
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Human EIF2B1 Protein expressed in Escherichia coli (E. coli) - ABIN667427
Mohammad-Qureshi, Haddad, Hemingway, Richardson, Pavitt: Critical contacts between the eukaryotic initiation factor 2B (eIF2B) catalytic domain and both eIF2beta and -2gamma mediate guanine nucleotide exchange. in Molecular and cellular biology 2007
Show all 2 references for ABIN667427
These are the first data that mechanistically link eIF2Bepsilon (show EIF2B5 Proteins) abundance to skeletal myofibre hypertrophy.
A point mutation in translation initiation factor (show TIF1 Proteins) eIF2B (show EIF2B4 Proteins) leads to Vanishing White Matter disease.
Inhibition of pancreatic protein synthesis in this model of acute pancreatitis most likely results from inhibition of translation initiation from increased eIF2alpha (show EIF2A Proteins) phosphorylation, reduction of eIF2B (show EIF2B4 Proteins) activity, and inhibition of eIF4F (show EIF4A2 Proteins) complex formation.
Oligodendrocytes with truncated or deletion mutants eIF2B showed less tolerable to endoplasmic reticulum stress
These data emphasize the importance of eIF2Balpha in mediating the eIF2 (show EIF2S1 Proteins) kinase translation-inhibitory activity and may provide insight into the complex nature of vesiculovirus oncolysis.
mutational analysis of the eIF2B genes of patients with an antenatal- or early-infantile-onset encephalopathy and an early demise
Biochemical analyses indicate that mutations analyzed in eIF2Balpha and -epsilon reduce the steady-state level of the affected subunit, while the most severe mutant tested, eIF2Bbeta(V341D), forms complexes with reduced stability and lower eIF2B activity.
analysis of novel mutations in patients with eIF2B-related disorders
Study reports 9 novel mutations in EIF2B genes in 8 patients, increasing number of known mutations to more than 120. Using homology modeling, analyzed the impact of novel mutations on the 5 subunits of eIF2B protein (alpha, beta, gamma, delta, epsilon)
The authors suspected VWM and sequenced the genes EIF2B1-5, which revealed one heterozygous mutation in EIF2B4 (show EIF2B4 Proteins).
Crystal structure of the alpha subunit (show POLG Proteins) of human translation initiation factor (show TIF1 Proteins) 2B.
This gene encodes one of five subunits of eukaryotic translation initiation factor 2B (EIF2B), a GTP exchange factor for eukaryotic initiation factor 2 and an essential regulator for protein synthesis. Mutations in this gene and the genes encoding other EIF2B subunits have been associated with leukoencephalopathy with vanishing white matter.
translation initiation factor eIF-2B subunit alpha
, Translation initiation factor eIF-2B subunit alpha
, translation initiation factor eif-2b subunit alpha
, eIF-2B GDP-GTP exchange factor subunit alpha
, eukaryotic translation initiation factor 2B, subunit 1 (alpha, 26kDa)
, GTP-exchange protein