Human Monokine Induced By Interferon Gamma (MIg) ELISA Kit EKU05998|产品详情|进口橙子视频旧款采购网

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Human Monokine Induced By Interferon Gamma (MIg) ELISA Kit

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Human Monokine Induced By Interferon Gamma (MIg) ELISA Kit

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货号：EKU05998

规格：96T

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Human Monokine Induced By Interferon Gamma (MIg) ELISA Kit

商品详情参考文献相关资料

Species Reactivity	Homo sapiens (Human)
Format	96 well plate
Detection Range	31.25-2000 pg/mL
Sensitivity	12.5 pg/mL
Sample Type	Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay Time	3 hours
UniProt	Q07325
Gene ID	4283
Gene Name	Monokine Induced By Interferon Gamma
Gene Aliases	CXCL9; CMK; Humig; MI-G; SCYB9; Crg-10; Chemokine (C-X-C motif) ligand 9; Small-inducible cytokine B9; Gamma-interferon-induced monokine
Application	ELISA
Assay Type	Sandwich
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 Monokine Induced By Interferon Gamma (MIg). No significant cross-reactivity or interference between Monokine Induced By Interferon Gamma (MIg) and analogues was observed.
Test Principle	The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Monokine Induced By Interferon Gamma (MIg). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Monokine Induced By Interferon Gamma (MIg). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Monokine Induced By Interferon Gamma (MIg), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Monokine Induced By Interferon Gamma (MIg) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Assay Precision	Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Monokine Induced By Interferon Gamma (MIg) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low,
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	Cytokine;