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上海恒遠(yuǎn)生物科技有限公司>技術(shù)文章>豬SIgA ELISA Kit

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豬SIgA ELISA Kit

閱讀:1931          發(fā)布時(shí)間:2011-11-29

      豬分泌型免疫球蛋白A(sIgA)ELISA Kit


FOR RESEARCH USE ONLY

Assay range1μg/ ml -40μg/ ml                     96 determinations

Purpose

This kit allows for the determination of SIgA concentrations in Porcine serum, cell culture supernates and other biological fluids 

Principle of the assay

The kit assay Porcine SIgA level in the sampleuse Purified Porcine SIgA antibody to coat microtiter plate wells, make solid-phase antibody, then add Porcine SIgA to wells, Combined antibody which With HRP labeled goat anti- Porcine become antibody - antigen - enzyme-antibody complex, after washing Compley, Add TMB substrate solution,TMB substrate becomes blue color At HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of  Porcine SIgA in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Materials provided with the kit

1

wash  solution

20ml×1bottle

7

Stopp Solution

6ml×1 bottle

2

HRP-Conjugate reagent

6ml×1 bottle

8

Standard80μg/ ml

0.5ml×1 bottle

3

Microelisa stripplate

12well×8strips

9

Standard diluent

1.5ml×1bottle

4

Sample diluent

6ml×1 bottle

10

Instruction

1

5

Chromogen Solution A

6ml×1 bottle

11

Closure plate membrane

2

6

Chromogen Solution B

6ml×1 bottle

12

Sealed bags

1

Specimen requirements

1.       extract as soon as possible after Specimen collection,and according to the relevant literature, and should be experiment as soon as possible after the extraction. If it can’t, specimen can be kept in -20 to preserve, Avoid repeated freeze-thaw cycles.

2.       Can’t detect the sample which contain NaN3, because NaN3 inhibits HRP active.

Assay procedure

1.       Dilute and add sample:Dilute Original density Standard as follow table:

40μg/ ml

5 Standard

150μl Original density Standard+150μl Standard diluent

20μg/ ml

4 Standard

150μl 5 Standard+150μl Standard diluent

10μg/ ml

3 Standard

150μl 4 Standard+150μl Standard diluent

5μg/ ml

2 Standard

150μl 3 Standard +150μl Standard diluent

2.5μg/ ml

1 Standard

150μl 2 Standard +150μl Standard diluent

2.add sampleSet blank wells separay (blank comparison wells don’t add sample and HRP-Conjugate reagent, other each step operation is same). testing sample well. add Sample dilution 40μl to testing sample well, then add testing sample 10μl (sample final dilution is 5-fold), add sample to wells , don’t touch the well wall as far as possible, and Gently mix.

3.Incubate: After closing plate with Closure plate membrane ,incubate for 30 min at 37.

4.Configurate liquid: 30-fold wash solution diluted 30-fold (or 20-fold) with distilled water and reserve.

5.washingUncover Closure plate membrane, discard Liquid, dry by swing, add washing buffer to every well, still for 30s then drain, repeat 5 times, dry by pat.

6.add enzymeAdd HRP-Conjugate reagent 50μl to each well, except  blank well.

7.incubateOperation with 3.

8.washingOperation with 5.

9.colorAdd Chromogen Solution A 50ul and Chromogen Solution B to each well, evade the light preservation for 15 min at 37

10.Stop the reactionAdd Stop Solution50μl to each well, Stop the reaction(the blue color change to yellow color).

11.assaytake blank well as zero , Read absorbance at 450nm after Adding Stop Solution and within 15min.

Steps description

Standard, Sample diluent

 

Add Standard, Sample diluent, incubate for 30 min at 37.

 

Wash 5 time,Add HRP-Conjugate reagent, incubate for 30 min at 37.

 

Wash 5 times,Add Chromogen Solution A and B, incubate for 30 min at 37.

 

Add Stopp Solution

 

Read absorbance at 450nm within 15 min

 

calculate

Calculate

Take the standard density as the horizontal, the OD value for the vertical ,draw the standard curve on graph paper, Find out the corresponding density according to the sample OD value by the Sample curve, multiplied by the dilution multiple, or calculate the straight line regression equation of the standard curve with the standard density and the OD value ,with the sample OD value in the equation, calculate the sample density, multiplied by the dilution factor, the result is the sample actual density.

Important notes

1.       The kit takes out from the refrigeration environment should be balanced 15-30 minutes in the room temperature, ELISA plates coated if has not use up after opened, the plate should be stored in Sealed bag.

2.       washing buffer will Crystallization separation, it can be heated the water helps dissolve when dilute . Washing does not affect the result.

3.       add Sample with sampler Each step, And proofread its accuracy frequently, avoids the experimental error. add sample within 5 min, if the number of sample is much , recommend to use Volley .

4.       if the testing material content is excessively higher (The sample OD is bigger than the first standard well ),please dilute Sample (n-fold), Please diluente and multiplied by the dilution factor.×n×5.

5.       Closure plate membrane only limits the disposable use, to avoid cross-contamination.

6.       The substrate evade the light preservation.

7.       Please according to use instruction strictly, The test result determination must take the microtiter plate reader as a standard.

8.       All samples, washing buffer and each kind of reject should according to infective material process.

9.       Do not mix reagents with those from other lots. 

Storage and validity

1Storage  2-8.

2validity six months.

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