{"product_id":"reed-biotech-s26a4-polyclonal-antibody-ra34657","title":"S26A4 Polyclonal Antibody","description":"\u003cp\u003esolute carrier family 26 member 4(SLC26A4) Homo sapiens Mutations 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\u0026amp;apos; of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008],\u003c\/p\u003e","brand":"Reed Biotech","offers":[{"title":"50 µL","offer_id":57250681487700,"sku":"ABM5039051-1","price":113.4,"currency_code":"GBP","in_stock":true},{"title":"100 µL","offer_id":57250681520468,"sku":"ABM5039051-2","price":153.0,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1040\/1782\/2036\/files\/Antibody_1_c79f8777-e204-4474-a23a-1e8495c34d87.webp?v=1790235121","url":"https:\/\/www.abmium.com\/es\/products\/reed-biotech-s26a4-polyclonal-antibody-ra34657","provider":"ABMIUM","version":"1.0","type":"link"}