Recombinant Human EIF4H Protein, Myc/DDK-tagged, C13 and N15-labeled

• Cat.No.: EIF4H-4894H
• Product Overview: EIF4H MS Standard C13 and N15-labeled recombinant protein (NP_071496) with a C-terminal MYC/DDK tag, was expressed in HEK293 cells.

Specification

• Species: Human
• Source: HEK293
• Tag: DDK&Myc
• Description: 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.
• Molecular Mass: 27.2 kDa
• AA Sequence: MADFDTYDDRAYSSFGGGRGSRGSAGGHGSRSQKELPTEPPYTAYVGNLPFNTVQGDIDAIFKDLSIRSVRLVRDKDTDKFKGFCYVEFDEVDSLKEALTYDGALLGDRSLRVDIAEGRKQDKGGFGFRKGGPDDRGMGSSRESRGGWDSRDDFNSGFRDDFLGGRGGSRPGDRRTGPPMGSRFRDGPPLRGSNMDFREPTEEERAQRPRLQLKPRTVATPLNQVANPNSAIFGGARPREEVVQKEQETRTRPLEQKLISEEDLAANDILDYKDDDDKV
• Purity: > 80% as determined by SDS-PAGE and Coomassie blue staining
• Stability: Stable for 3 months from receipt of products under proper storage and handling conditions.
• Storage: Store at -80 centigrade. Avoid repeated freeze-thaw cycles.
• Concentration: 50 μg/mL as determined by BCA
• Storage Buffer: 100 mM glycine, 25 mM Tris-HCl, pH 7.3.

Gene Information

• Gene Name: EIF4H eukaryotic translation initiation factor 4H [ Homo sapiens (human) ]
• Official Symbol: EIF4H
• Synonyms: EIF4H; eukaryotic translation initiation factor 4H; WBSCR1, Williams Beuren syndrome chromosome region 1; KIAA0038; WSCR1; Williams-Beuren syndrome chromosome region 1; WBSCR1; eIF-4H
• Gene ID: 7458
• mRNA Refseq: NM_022170
• Protein Refseq: NP_071496
• MIM: 603431
• UniProt ID: Q15056