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Home >> Antibodies >> EIF2S3 Antibody / Eukaryotic translation initiation factor 2 subunit 3 Antibody

EIF2S3 Antibody / Eukaryotic translation initiation factor 2 subunit 3 Antibody (FY13619)

  Catalog No Formulation Size Price (USD)  
Image FY13619 0.5mg/ml if reconstituted with 0.2ml sterile DI water 100 ug 449
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EIF2S3 Antibody by FACS in K562 cells. Flow cytometry using Eukaryotic translation initiation factor 2 subunit 3 Antibody shows a rightward fluorescence shift in fixed, permeabilized K562 cells stained with primary antibody (blue histogram), compared with the rabbit IgG isotype control (green) and unstained blank control (red). Cells were fixed in 4% paraformaldehyde, permeabilized, and blocked with 10% normal goat serum. Primary antibody was applied at 1 ug per million cells for 30 minutes, followed by Fluoro488-conjugated secondary antibody. This assay demonstrates intracellular rather than cell-surface staining.
EIF2S3 Antibody by WB in human cell lines. Western blot analysis using Eukaryotic translation initiation factor 2 subunit 3 Antibody detects an immunoreactive band consistent with the expected molecular weight of approximately 51 kDa. Lane assignments: HeLa (lane 1), K562 (lane 2), SiHa (lane 3). Each lane contained 30 ug total protein under reducing conditions, resolved by 10% SDS-PAGE and transferred to nitrocellulose. Membranes were blocked with 5% nonfat milk and incubated with primary antibody at 0.5 ug/mL overnight at 4oC. An HRP-conjugated secondary antibody and chemiluminescent substrate were used for detection.
EIF2S3 Antibody by IHC in human testicular carcinoma. Immunohistochemistry of formalin-fixed, paraffin-embedded human testicular carcinoma using Eukaryotic translation initiation factor 2 subunit 3 Antibody shows brown cytoplasmic staining in a subset of tumor cells. Antigen retrieval was performed with EDTA buffer at pH 8.0. Sections were blocked with 10% goat serum and incubated with primary antibody at 2 ug/mL overnight at 4oC. Detection used an HRP-conjugated secondary antibody and DAB chromogen, with hematoxylin counterstaining.
Species Reactivity Human, Mouse, Rat
Format Antigen affinity purified
Host Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit Ig
Buffer Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
UniProt P41091
Applications Western Blot : 0.5-1ug/ml
Immunohistochemistry (FFPE) : 2-5ug/ml
Flow Cytometry : 1-3ug/million cells
ELISA : 0.1-0.5 ug/ml
Limitations For research use only, this EIF2S3 Antibody / Eukaryotic translation initiation factor 2 subunit 3 Antibody is not intended for diagnostic or therapeutic use.
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Description

EIF2S3 Antibody / Eukaryotic translation initiation factor 2 subunit 3 Antibody recognizes the gamma subunit of eukaryotic translation initiation factor 2, a central component of the machinery that begins protein synthesis. The EIF2S3 gene encodes the GTP-binding subunit of the eIF2 heterotrimer, which also contains alpha and beta subunits. During initiation, eIF2 binds GTP and initiator methionyl-tRNA to form a ternary complex. This complex delivers the initiator tRNA to the small ribosomal subunit as the ribosome prepares to identify a translation start codon.

The gamma subunit supplies the nucleotide-binding core and contributes to the recognition of initiator tRNA. Once the scanning ribosomal complex identifies an appropriate start site, GTP hydrolysis and subsequent factor release permit progression toward assembly of an elongation-competent ribosome. The nucleotide state of eIF2 must then be reset by the guanine nucleotide exchange factor eIF2B. These linked reactions make initiation sensitive to both the availability of charged initiator tRNA and the regulatory state of the eIF2 system.

The EIF2S3 Antibody recognizes the gamma subunit, which performs the nucleotide-binding function that distinguishes its contribution from those of the alpha and beta subunits. One major control mechanism is the integrated stress response. Cellular stresses activate kinases that phosphorylate the alpha subunit of eIF2, converting the complex into an inhibitor of productive nucleotide exchange by eIF2B. This reduces overall initiation while favoring translation of selected transcripts with specialized regulatory features, including ATF4. Although EIF2S3 itself is not the principal phosphorylation target, the activity of its GTP-binding subunit is inseparable from this regulated cycle. Changes in ternary-complex availability can therefore reshape protein synthesis across the cell.

Pathogenic EIF2S3 variants cause an X-linked neurodevelopmental disorder commonly associated with MEHMO syndrome, which can involve microcephaly, epilepsy, developmental impairment, hypogonadism, and obesity. These phenotypes show that even a broadly required translation factor can have especially pronounced consequences in developing tissues. The relationship between particular EIF2S3 variants, initiation efficiency, and tissue-specific vulnerability remains important for understanding how altered protein synthesis produces complex developmental disease.

Explore related research targets in our Cell Biology Antibodies collection.

Application Notes

Investigators should determine the optimal dilution of the EIF2S3 Antibody / Eukaryotic translation initiation factor 2 subunit 3 Antibody empirically for their experimental conditions.

Immunogen

The EIF2S3 Antibody was generated using e. coli-derived human EIF2S3 recombinant protein (amino acids Q12-D472).

Storage

After reconstitution, keep the EIF2S3 Antibody at 4oC for up to one month. Alternatively, store aliquots at -20oC for up to six months. Avoid multiple freezing and thawing cycles.

Alternate Names

EIF2S3 antibody, Eukaryotic translation initiation factor 2 subunit 3 antibody, eukaryotic translation initiation factor 2 subunit gamma antibody, EIF2G antibody, EIF2 antibody, eIF 2gX antibody, eIF 2gA antibody, eIF 2 gamma X antibody

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