{"product_id":"new-product-815224","title":"COL11A2 Rabbit pAb","description":"\u003cp\u003eThis gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline\/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6.\u003c\/p\u003e","brand":"Abclonal","offers":[{"title":"100ul","offer_id":46092339445984,"sku":"A10473","price":298.0,"currency_code":"KRW","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0601\/9330\/8896\/files\/A10473_1.jpg?v=1721950839","url":"https:\/\/rndmate.com\/products\/new-product-815224","provider":"알앤디메이트","version":"1.0","type":"link"}