Search
Search
Invitrogen
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promotions']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.viewpromo']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promocode']}}: {{promo.promoCode}} {{promo.promoTitle}} {{promo.promoDescription}}. {{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.learnmore']}}
This gene encodes a member of the cytoskeletal BTB/kelch repeat family. The encoded protein plays a role in neurofilament architecture and is involved in mediating the ubiquitination and degradation of some proteins. Defects in this gene are a cause of giant axonal neuropathy.
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: gan; giant axonal neuropathy; Gigaxonin; kelch-like family member 16; Kelch-like protein 16
基因别名: A330045G18; GAN; GAN1; gigaxonin; KLHL16
UniProt ID: (Human) Q9H2C0, (Mouse) Q8CA72
Entrez Gene ID: (Human) 8139, (Rat) 307893, (Mouse) 209239