{"product_id":"abm190001","title":"STRUM Rabbit Polyclonal Antibody","description":"\u003ch3\u003eBackground\u003c\/h3\u003e\u003cp\u003eThis gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive| lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases.\u003c\/p\u003e","brand":"BT LAB","offers":[{"title":"20ul","offer_id":57661408903508,"sku":"ABM190001","price":69.0,"currency_code":"GBP","in_stock":true},{"title":"50ul","offer_id":57661408936276,"sku":"ABM190002","price":115.0,"currency_code":"GBP","in_stock":true},{"title":"100ul","offer_id":57661408969044,"sku":"ABM190003","price":176.0,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1040\/1782\/2036\/files\/btlab-d2d7dbc8ab9867d9bfb47270975b8ed0a2fec16d8ca385af99d399426c28f9c5.jpg?v=1792159015","url":"https:\/\/www.abmium.com\/de\/products\/abm190001","provider":"ABMIUM","version":"1.0","type":"link"}