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']}}
Immunogen sequence: PESNLVYWLW EKQKVMAIVR IDTQNNPVYQ VSFSPQDNTQ VCVTGNGMFK LLRFAEGTLK QTSFQRGEPQ NYLAHTWVAD DKIVVGTDTG KLFLFESGDQ RWETSIMVKE PTNGSKSLDV IQESESLIEF PPVSSPLP
Highest antigen sequence identity to the following orthologs: Mouse - 78%, Rat - 21%.
The WDR65 gene, which stands for WD Repeat Domain 65, encodes a protein characterized by the presence of WD repeat domains that facilitate protein-protein interactions. This gene is implicated in the assembly of a subset of inner arm dyneins, critical for ciliary motility and axonemal structure. Mutations in WDR65 have been associated with diseases such as Van der Woude syndrome (VWS) and related craniofacial disorders, highlighting its role in developmental processes. Specifically, a missense mutation in WDR65 was identified as a potential cause of VWS, suggesting that WDR65 is a target for regulatory factors like IRF6.
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: Cilia- and flagella-associated protein 57; WD repeat-containing protein 65
基因别名: CFAP57; VWS2; WDR65
UniProt ID: (Human) Q96MR6
Entrez Gene ID: (Human) 149465