TSH ELISA Kit

2017-08-29

　　Generic Name: thyrotropin quantitative detection kit (ELISA)

　　English name: TSH ELISA Kit

　　[Medical Device Manufacturing Enterprise License No.】 Beijing Drug Administration firearms production Xu 20,040,085 No.

　　[Medical Device Registration Certificate No.] SFDA (quasi-) word 2006 3400254 No.

 

▲ Product name

　　Generic Name: thyrotropin quantitative detection kit (ELISA)

　　English name: TSH ELISA Kit

　　[Medical Device Manufacturing Enterprise License No.】 Beijing Drug Administration firearms production Xu 20,040,085 No.

　　[Medical Device Registration Certificate No.] SFDA (quasi-) word 2006 3400254 No.

 

▲ Packing

　　96 / box, 480 / box

 

▲ intended use

　　For the quantitative detection of the acquisition on the S & S 903 # filter paper blood samples of newborns thyroid stimulating hormone (TSH) concentrations for neonatal hypothyroidism screening.

 

▲ Applicable models

　　Microplate reader. The description of the technical parameters of the company's US DYNEX CB 372 microplate reader. Wavelength of 450 ± 10nm.

 

▲ Products

　　Children Urine enzyme phenylalanine metabolic pathway caused by defects in benzene emit large amounts of metabolites phenylalanine disease, known as phenylketonuria, it is an autosomal recessive genetic disease. Phenylalanine hydroxylase is a special liver enzyme that congenital deficiency or decreased activity not normally lead to hydroxylation of phenylalanine to tyrosine, but into the human circulation, making the blood, cerebrospinal fluid and urine of benzene alanine increased. The disease is often accompanied by inhibition of tyrosinase tyrosine metabolism.

　　Phenylalanine, phenylpyruvic acid, phenylacetic acid accumulation can cause brain and other developmental disorders, myelination blocked, gray degeneration, and causes mental retardation in infants, often occurs before the age of seizures, infantile spasms and even have similar Clinical manifestations of disease and EEG peak imperfectly, children may also have movement disorders, cerebral palsy, hyperactivity, tremors and vomiting, anxiety, eczema and other symptoms.

　　Neonatal screening for early detection of phenylalanine in children, and in a timely manner a low-phenylalanine diet therapy, so that children maintain blood phenylalanine at 1-2mg / dl, thereby preventing severe mental disorders and continue the occurrence of idiopathic epilepsy and other diseases, has important clinical significance.