カタログ製品コード : C-EK12042
Human Apolipoprotein A1/Apo A1 ELISA kit
24T | ¥53,200 | (¥2,217/T) (税別) |
48T | ¥67,200 | (¥1,400/T) (税別) |
96T | ¥76,000 | (¥792/T) (税別) |
標準納期 : 2週間 |
カタログ製品コード : C-EK12042
Human Apolipoprotein A1/Apo A1 ELISA kit
24T | ¥53,200 | (¥2,217/T) (税別) |
48T | ¥67,200 | (¥1,400/T) (税別) |
96T | ¥76,000 | (¥792/T) (税別) |
標準納期 : 2週間 |
メーカー名 | 遺伝子名 | 種交差性 | 測定範囲 | サンプル量 | 適用サンプル | ドキュメント |
---|---|---|---|---|---|---|
MultiSciences | Apolipoprotein A1/Apo A1 | Human | 3.13 - 200 ng/ml | 10 μl (prediluted) | 血清、血漿、細胞培養上清 |
■保存方法 :
キットは未開封の場合、4℃で保管すること。 開封後は標準溶液を-20℃で保存し、他の試薬は4℃で保存すること。
■構成内容 :
96-well polystyrene microplate coated with a monoclonal antibody against Apo A1 |
Human Apo A1 Standard, lyophilized |
Apo A1 Detect Antibody |
Streptavidin-HRP |
Assay Buffer (10×) |
Substrate (TMB) |
Stop Solution |
Washing Buffer (20×) |
Plate Covers |
■キーワード :
Homo sapiens,Human,Apolipoprotein A-I,Apo-AI,ApoA-I,Apolipoprotein A1,APOA1
■ターゲット情報 :
This assay employs the quantitative sandwich enzyme immunoassay technique for the quantitative detection of human Apo A1. The Human Apolipoprotein A1/Apo A1 ELISA is for research use only. Not for diagnostic or therapeutic procedures.
Apolipoprotein A1 (Apo A1) is the major protein component of high density lipoprotein (HDL) in plasma. Chylomicrons secreted from the intestinal enterocyte also contain Apo A1, but it is quickly transferred to HDL in the bloodstream. The protein has a specific role in lipid metabolism. It promotes fat efflux, including cholesterol, from tissues to the liver for excretion. It is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. Apo A1 was also isolated as a prostacyclin (PGI2) stabilizing factor, and thus may have an anticlotting effect.
Apo A1 is often used as a biomarker for prediction of cardiovascular diseases and the ratio Apo B-100/Apo A1 has been reported as a stronger predictor for the risk of myocardial infarction than any other lipid measurement. Defects in the gene encoding it are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis.