Genemedi produces core diagnostic ingredients for test of Metabolic diseases (S-adenosylhomocysteine (AdoHcy) hydrolase deficiency) and related syndrome. GeneMedi offers paired diagnostics grade S-adenosylhomocysteine (AdoHcy) hydrolase (SAHH) antibodies (monoclonal antibody, mab) and antigens for Metabolic diseases (S-adenosylhomocysteine (AdoHcy) hydrolase deficiency) rapid test kit of S-adenosylhomocysteine (AdoHcy) hydrolase (SAHH) testing in standard substance, positive control, ELISA test,Lateral flow immunoassay (LFIA),colloidal gold immunochromatographic assay, Chemiluminescent immunoassay (CLIA),turbidimetric inhibition immuno assay (TINIA), immunonephelometry and POCT. All the antibodies and antigens for Metabolic diseases (S-adenosylhomocysteine (AdoHcy) hydrolase deficiency ) test are suitable for in functional ELISA, and other immunoassays in dignostics.The antibodies can act as a capture antibody and detection antibody. The antigens can be used as positive control.S-adenosylhomocysteine (AdoHcy) hydrolase (E.C.3.3.1.1) hydrolysis adenosine and homocysteine. In eukaryotes, this is the major route for disposal of the AdoHcy formed as a common product of each of many S-adenosylmethionine (AdoMet)-dependent methyltransferases. The reaction is reversible, but under normal conditions the removal of both adenosine and homocysteine is sufficiently rapid to maintain the flux in the direction of hydrolysis. AdoHcy is an inhibitor of many AdoMet-dependent methyltransferases. Thus, AdoHcy hydrolysis serves physiologically not only to sustain the flux of methionine sulfur toward cysteine, but is believed also to play a critical role in the regulation of biological methylations. The deficiency of AdoHcy leads to hypotonia with elevated serum creatine kinase and transaminases, prolonged prothrombin time and low albumin.