EIF4H Antibody (Center) Blocking peptide
€363.00
In stock
SKU
AC-BP12612c
Background:
This gene encodes one of the translation initiationfactors, which functions to stimulate the initiation of proteinsynthesis at the level of mRNA utilization. This gene is deleted inWilliams syndrome, a multisystem developmental disorder caused bythe deletion of contiguous genes at 7q11.23. Alternative splicingof this gene generates 2 transcript variants.
Other Names:
Eukaryotic translation initiation factor 4H, eIF-4H, Williams-Beuren syndrome chromosomal region 1 protein, EIF4H, KIAA0038, WBSCR1, WSCR1
Gene Name: EIF4H
Gene ID: 7458
Primary Accession: Q15056
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes one of the translation initiationfactors, which functions to stimulate the initiation of proteinsynthesis at the level of mRNA utilization. This gene is deleted inWilliams syndrome, a multisystem developmental disorder caused bythe deletion of contiguous genes at 7q11.23. Alternative splicingof this gene generates 2 transcript variants.
Other Names:
Eukaryotic translation initiation factor 4H, eIF-4H, Williams-Beuren syndrome chromosomal region 1 protein, EIF4H, KIAA0038, WBSCR1, WSCR1
Gene Name: EIF4H
Gene ID: 7458
Primary Accession: Q15056
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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