{"product_id":"s26a4-polyclonal-antibody-50ul","title":"S26A4 Polyclonal Antibody, 50ul","description":"\u003cp\u003eMutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. \u003c\/p\u003e","brand":"BT LAB","offers":[{"title":"Default Title","offer_id":56516024762741,"sku":"BT-AP14005-50ul","price":162.0,"currency_code":"EUR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0843\/2671\/1640\/files\/Antibody_main_1.jpg?v=1766393459","url":"https:\/\/www.labcart.com\/products\/s26a4-polyclonal-antibody-50ul","provider":"LabCart Life Science","version":"1.0","type":"link"}