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: AVTLEAPFLD VLNTMMDTTL PLTLEELEEW GNPSSDEKHK NYIKRYCPYQ NIKPQHYPSI HITAYENDER VPLKGIVSYT EKLKEAIAEH AKDTGEGYQT PNIILDIQPG GNHVIEDSHK KITAQIKFLY EELGLDSTSV FEDLKKYLKF; Positive Samples: U-87MG, Mouse brain, Rat brain; Cellular Location: Cytoplasm, cytosol
The protein encoded by this gene belongs to the prolyl oligopeptidase subfamily of serine peptidases. Mutations in this gene have been associated with hypotonia-cystinuria syndrome, also known as the 2p21 deletion syndrome.
⚠WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.
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: Prolyl endopeptidase-like; Prolylendopeptidase-like; putative prolyl oligopeptidase
基因别名: 2810457N15Rik; 9530014L06Rik; D030028O16Rik; KIAA0436; mKIAA0436; PREPL; RGD1310143
UniProt ID: (Human) Q4J6C6, (Mouse) Q8C167, (Rat) Q5HZA6
Entrez Gene ID: (Human) 9581, (Mouse) 213760, (Rat) 298771