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Antibody detects endogenous levels of total EIF4H.
This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: eIF-4H; Eukaryotic translation initiation factor 4H; Williams-Beuren syndrome chromosomal region 1 protein; Williams-Beuren syndrome chromosomal region 1 protein homolog; Williams-Beuren syndrome chromosome region 1; Williams-Beuren syndrome chromosome region 1 homolog
基因别名: AU018978; D5Ertd355e; E430026L18Rik; Ef4h; eIF-4H; EIF4H; KIAA0038; mKIAA0038; WBSCR1; WSCR1
UniProt ID: (Human) Q15056, (Mouse) Q9WUK2
Entrez Gene ID: (Human) 7458, (Mouse) 22384