{"id":4074,"date":"2021-02-26T08:23:04","date_gmt":"2021-02-26T08:23:04","guid":{"rendered":"https:\/\/vospan.com\/?post_type=product&p=4074"},"modified":"2022-04-12T08:39:25","modified_gmt":"2022-04-12T08:39:25","slug":"hplc-kit-for-pku","status":"publish","type":"product","link":"https:\/\/vospan.com\/en\/san-pham\/hplc-kit-for-pku\/","title":{"rendered":"HPLC KIT FOR PKU"},"content":{"rendered":"
Phenylketonuria, also called PKU, is a rare inherited disorder that causes an amino acid called
\nphenylalanine to build up in the body. PKU is caused by a defect in the gene that helps create the
\nenzyme needed to break down phenylalanine.
\nWithout the enzyme necessary to process phenylalanine, a dangerous buildup can develop when a
\nperson with PKU eats foods that contain protein or eats aspartame, an artificial sweetener. This can
\neventually lead to serious health problems.
\nFor the rest of their lives, people with PKU \u2014 babies, children and adults \u2014 need to follow a diet
\nthat limits phenylalanine, which is found mostly in foods that contain protein.
\nBabies are screened for PKU soon after birth. Recognizing PKU right away can help prevent major
\nhealth problems.
\nIt can be quantitatively determined by the Jasem PKU HPLC Analysis Kit.<\/p>\n","protected":false},"excerpt":{"rendered":"