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Eukaryotic Translation Initiation Factor 2B, Subunit 2 Beta, 39kDa Proteins (EIF2B2)

EIF2B2 encodes the beta subunit of eukaryotic initiation factor-2B (EIF2B). Additionally we are shipping EIF2B2 Antibodies (47) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
EIF2B2 217715 Q99LD9
Rat EIF2B2 EIF2B2 84005  
EIF2B2 8892 P49770
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Top EIF2B2 Proteins at antibodies-online.com

Showing 7 out of 7 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
Yeast Cow His tag   1 mg Log in to see 56 to 66 Days
$2,955.33
Details
Yeast Rabbit His tag   1 mg Log in to see 56 to 66 Days
$2,955.33
Details
Yeast Takifugu rubripes His tag   1 mg Log in to see 56 to 66 Days
$2,968.17
Details
HOST_Human Human Un-conjugated   20 μg Log in to see 9 to 11 Days
$785.40
Details

EIF2B2 Proteins by Origin and Source

Origin Expressed in Conjugate
Mouse (Murine)

Human , ,
,

More Proteins for Eukaryotic Translation Initiation Factor 2B, Subunit 2 Beta, 39kDa (EIF2B2) Interaction Partners

Human Eukaryotic Translation Initiation Factor 2B, Subunit 2 Beta, 39kDa (EIF2B2) interaction partners

  1. An Italian patient is described with a c.638A>G mutation in exon 5 of EIF2B2 gene with very slow progressive vanishing white matter disease.

  2. analysis of vanishing white matter disease caused by EIF2B2 mutation with the presentation of an adrenoleukodystrophy phenotype [case report]

  3. Mutation in EIF2B2 causes childhood ataxia (show USP14 Proteins) with central nervous system hypomyelination/ vanishing white matter leukodystrophy.

  4. 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 (show EIF2B1 Proteins) activity.

  5. The role of the residues Ser2 and Ser67 contribute to the important role of the N-terminal region of eIF2beta for its function in mammals.

  6. CACH (show EIF2B5 Proteins) syndrome is linked to mutations in the five EIF2B (show EIF2B1 Proteins)--REVIEW

  7. Study reports 9 novel mutations in EIF2B (show EIF2B1 Proteins) genes in 8 patients, increasing number of known mutations to >120. Using homology modeling, analyzed the impact of novel mutations on the 5 subunits of eIF2B (show EIF2B1 Proteins) protein (alpha, beta, gamma, delta, epsilon).

EIF2B2 Protein Profile

Protein Summary

This gene encodes the beta subunit of eukaryotic initiation factor-2B (EIF2B). EIF2B is involved in protein synthesis and exchanges GDP and GTP for its activation and deactivation.

Gene names and symbols associated with EIF2B2

  • eukaryotic translation initiation factor 2B, subunit 2 beta (Eif2b2)
  • eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa (EIF2B2)
  • AA409345 protein
  • C85417 protein
  • EIF-2Bbeta protein
  • EIF2B protein

Protein level used designations for EIF2B2

eIF-2B GDP-GTP exchange factor subunit beta , translation initiation factor eIF-2B subunit beta , eukaryotic translation initiation factor 2B, subunit 2 (beta, 39kD) , S20I15 , S20III15 , protein synthesis initiation factor eIF-2B beta subunit

GENE ID SPECIES
217715 Mus musculus
84005 Rattus norvegicus
8892 Homo sapiens
513958 Bos taurus
100009318 Oryctolagus cuniculus
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