Gene: EIF4H
Official Full Name: eukaryotic translation initiation factor 4Hprovided by HGNC
Gene Summary: 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. [provided by RefSeq, Jul 2008]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA13139 | EIF4H Knockout cell line (AC16) | Human | EIF4H | 1:3-1:4 | negative | Online Inquiry |
| KOA28578 | EIF4H Knockout cell line (BEAS-2B) | Human | EIF4H | 1:3~1:4 | negative | Online Inquiry |
| KOA44015 | EIF4H Knockout cell line (U-2932) | Human | EIF4H | 1:2-1:4 | negative | Online Inquiry |
| KOA59395 | EIF4H Knockout cell line (TPC-1) | Human | EIF4H | 1:5-1:8 | negative | Online Inquiry |
| KOA74820 | EIF4H Knockout cell line (NCM460) | Human | EIF4H | 1:2~1:3 | negative | Online Inquiry |
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