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Androstenediol (AED) ELISA Kit

品牌：Biomatik

貨號(hào)：EKU02345

規(guī)格：96T

貨期：

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Androstenediol (AED) ELISA Kit

商品詳情參考文獻(xiàn) 相關(guān)資料

Species Reactivity	Multispecies (General)
Format	96 well plate
Detection Range	123.46-10000 pg/mL
Sensitivity	49.5 pg/mL
Sample Type	Serum, plasma and other biological fluids
Assay Time	2 hours
Gene Name	Androstenediol
Gene Aliases	5-AED; 5AED; 5-Androstenediol; Androst-5-Ene-3Beta,17Beta-Diol
Application	ELISA
Assay Type	Competitive
Detection Method	Colorimetric
Shipping Condition	Blue ice
Storage Instructions	-20 °C. Bring all reagents to room temperature before beginning test. The kit may be stored at 4°C for immediate use within two days upon arrival. Reseal any unused strips with desiccant pack. Minimize freeze/thaw cycles.
Precaution Of Use	The Stop Solution is acidic. Do not allow to contact skin or eyes. Calibrators, controls and specimen samples should be assayed in duplicate. Once the procedure has been started, all steps should be completed without interruption.
Expiry Date	8 months
Specificity	This assay has high sensitivity and excellent specificity for detection of Androstenediol (AED). No significant cross-reactivity or interference between Androstenediol (AED) and analogues was observed.
Test Principle	This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Androstenediol (AED) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Androstenediol (AED) and unlabeled Androstenediol (AED) (Standards or samples) with the pre-coated antibody specific to Androstenediol (AED). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Androstenediol (AED) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Androstenediol (AED) in the sample.
Assay Precision	Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Androstenediol (AED) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level
Stability	The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition. To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
Restrictions	For research use only. Not for diagnostic procedures.
Quality Systems	The Kit is manufactured at ISO 9001 and ISO 13485 certified facilities.
Research Area	Endocrinology;Reproductive science;Hormone metabolism;