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: TWTELCPMIE ARKNHGLVFV KDKIFAVGGQ NGLGGLDNVE YYDIKLNEWK MVSPMPWKGV TVKCAAVGSI VYVLAGFQGV GRLGHILEYN TETDKWVANS KVRAFPVTSC LICVVDTCGA NE
Highest antigen sequence identity to the following orthologs: Mouse - 95%, Rat - 96%.
Defects in KLHL7 are the cause of retinitis pigmentosa type 42 (RP42). The specific function of this protein remains unknown.
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: kelch-like 6; kelch-like 7; kelch-like family member 7; Kelch-like protein 7; kelch/BTB
基因别名: KLHL6; KLHL7; SBBI26
UniProt ID: (Human) Q8IXQ5, (Rat) Q5XHZ6
Entrez Gene ID: (Human) 55975, (Rat) 362303