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: TLTGKNYTME WYELFQLGNC TFPHLRPEMD APFWCNQGAA CFFEGIDDVH WKENGTLVQV ATISGNMFNQ MAKWVKQDNE TGIYYETWNV KASPEK
Highest antigen sequence identity to the following orthologs: Mouse - 83%, Rat - 85%.
This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008].
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: Bis(monoacylglycero)phosphate synthase CLN5; BMP synthase CLN5; ceroid-lipofuscinosis; Ceroid-lipofuscinosis neuronal protein 5; Palmitoyl protein thioesterase CLN5; Protein CLN5; S-depalmitoylase CLN5
基因别名: BMPS; CLN5; NCL
UniProt ID: (Human) O75503
Entrez Gene ID: (Human) 1203