ATP結(jié)合盒轉(zhuǎn)運(yùn)蛋白G1(ABCG1)檢測(cè)試劑盒

適用生物 Homo sapiens (Human，人)
ATP結(jié)合盒轉(zhuǎn)運(yùn)蛋白G1(ABCG1)檢測(cè)試劑盒檢測(cè)范圍 0.156-10ng/mL 靈敏度 0.063ng/mL
樣本類型 Tissue homogenates, cell lysates and other biological fluids.
實(shí)驗(yàn)時(shí)長(zhǎng) 4.5h 實(shí)驗(yàn)方法 雙抗夾心法 ATP結(jié)合盒轉(zhuǎn)運(yùn)蛋白G1(ABCG1)檢測(cè)試劑盒規(guī)格 96T

ELISA Kit for ATP Binding Cassette Transporter G1 (ABCG1)

FOR IN VITRO AND RESEARCH USE ONLY, NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES!

ATP結(jié)合盒轉(zhuǎn)運(yùn)蛋白G1(ABCG1)檢測(cè)試劑盒Specificity

This assay has high sensitivity and excellent specificity for detection of ATP Binding Cassette Transporter G1 (ABCG1).
No significant cross-reactivity or interference between ATP Binding Cassette Transporter G1 (ABCG1) and analogues was observed.

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level ATP Binding Cassette Transporter G1 (ABCG1) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level ATP Binding Cassette Transporter G1 (ABCG1) 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 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.

ATP結(jié)合盒轉(zhuǎn)運(yùn)蛋白G1(ABCG1)檢測(cè)試劑盒Reagents and materials provided

Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 100μL standard or sample to each well. Incubate 2 hours at 37^oC;
3. Aspirate and add 100μL prepared Detection Reagent A. Incubate 1 hour at 37^oC;
4. Aspirate and wash 3 times;
5. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37^oC;
6. Aspirate and wash 5 times;
7. Add 90μL Substrate Solution. Incubate 15-25 minutes at 37^oC;
8. Add 50μL Stop Solution. Read at 450nm immediay.

ATP結(jié)合盒轉(zhuǎn)運(yùn)蛋白G1(ABCG1)檢測(cè)試劑盒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 ATP Binding Cassette Transporter G1 (ABCG1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to ATP Binding Cassette Transporter G1 (ABCG1). 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 ATP Binding Cassette Transporter G1 (ABCG1), 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 ATP Binding Cassette Transporter G1 (ABCG1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.