吲哚乙酸(IAA)檢測(cè)試劑盒

適用生物 General，通用
吲哚乙酸(IAA)檢測(cè)試劑盒檢測(cè)范圍 2.47-200ng/mL 靈敏度 0.87ng/mL
樣本類型 Tissue or cell culture supernates.
實(shí)驗(yàn)時(shí)長(zhǎng) 2.5h 實(shí)驗(yàn)方法 競(jìng)爭(zhēng)抑制法 吲哚乙酸(IAA)檢測(cè)試劑盒規(guī)格 96T
ELISA Kit for Indole 3 Acetic Acid (IAA)
FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!

Organism species General
吲哚乙酸(IAA)檢測(cè)試劑盒Sample type Tissue or cell culture supernates.
Format 96-well strip plate
Assay length 2.5 hours
Detection range 2.47-200ng/mL The standard curve concentrations used for the ELISA’s were 200ng/mL, 66.67ng/mL, 22.22ng/mL, 7.41ng/mL, 2.47ng/mL
Sensitivity The minimum detectable dose of this kit is typically less than 0.87ng/mL.

Specificity
This assay has high sensitivity and excellent吲哚乙酸(IAA)檢測(cè)試劑盒 specificity for detection of Indole 3 Acetic Acid (IAA).
No significant cross-reactivity or interference between Indole 3 Acetic Acid (IAA) and analogues was observed.
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Indole 3 Acetic Acid (IAA) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Indole 3 Acetic Acid (IAA) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
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吲哚乙酸(IAA)檢測(cè)試劑盒 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.
Reagents and materials provided

Reagents Quantity Reagents Quantity
Pre-coated, ready to use 96-well strip plate 1 Plate sealer for 96 wells 4
Standard 2 Standard Diluent 1×20mL
Detection Reagent A 1×120μL Assay Diluent A 1×12mL
Detection Reagent B 1×120μL Assay Diluent B 1×12mL
TMB Substrate 1×9mL Stop Solution 1×6mL
Wash Buffer (30 × concentrate) 1×20mL Instruction manual 1

Assay procedure summary
1. Prepare all reagents, samples and standards;
2. Add 50μL standard or sample to each well.
    And then add 50μL prepared Detection Reagent A immediay.
    Shake and mix. Incubate 1 hour at 37oC;
3. Aspirate and wash 3 times;
4. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37oC;
5. Aspirate and wash 5 times;
6. Add 90μL Substrate Solution. Incubate 15-25 minutes at 37oC;
7. Add 50μL Stop Solution. Read at 450 nm immediay.
Test principle
This assay employs the competitive 吲哚乙酸(IAA)檢測(cè)試劑盒inhibition enzyme immunoassay technique. A monoclonal antibody specific to Indole 3 Acetic Acid (IAA) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Indole 3 Acetic Acid (IAA) and unlabeled Indole 3 Acetic Acid (IAA) (Standards or samples) with the pre-coated antibody specific to Indole 3 Acetic Acid (IAA). 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 Indole 3 Acetic Acid (IAA) in the sample. 吲哚乙酸(IAA)檢測(cè)試劑盒After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Indole 3 Acetic Acid (IAA) in the sample.