四虎成人精品国产永久免费无码,久久午夜夜伦鲁鲁片免费无码影视,丝瓜视频在线观看,国产精品女同久久久久电影院

歡迎來到凱學(xué)生物科技(上海)有限公司網(wǎng)站!

熱門關(guān)鍵詞:進(jìn)口ELISA試劑盒,人ELISA試劑盒,大鼠elisa試劑盒價(jià)格,小鼠elisa試劑盒價(jià)格,豬elisa試劑盒,雞elisa試劑盒,兔elisa試劑盒,魚elsa試劑盒,其他種屬elisa試劑盒,豚鼠elisa試劑盒,倉(cāng)鼠elisa試劑盒,裸鼠ELISA試劑盒,進(jìn)口試劑,血清,動(dòng)物血清,人血清,胎牛血清,氨基酸試劑,培養(yǎng)基,顯色培養(yǎng)基,大腸桿菌O157培養(yǎng)基,細(xì)菌總數(shù)培養(yǎng)基,金黃色葡萄球菌檢驗(yàn)培養(yǎng)基,沙門氏菌/賀氏菌檢驗(yàn)培養(yǎng)基, 弧菌檢驗(yàn)培養(yǎng)基,其他培養(yǎng)基,酵母 霉菌 青霉 曲霉培養(yǎng)基, 李斯特氏菌檢驗(yàn)培養(yǎng)基,抗體,二抗,一抗,生物試劑,酶生物試劑,蛋白質(zhì)試劑,抗生素試劑,植物激素及核酸試劑,碳水化合物試劑,色素試劑,維生素試劑,表面活性劑,緩沖試劑,其他生化試劑,標(biāo)準(zhǔn)品對(duì)照品類,對(duì)照品,對(duì)照藥材,標(biāo)準(zhǔn)品,標(biāo)準(zhǔn)試劑,Spectrum試劑,美國(guó)藥典級(jí)試劑等

資料下載您現(xiàn)在的位置:首頁(yè) > 資料下載 > 人腫瘤壞死因子α(TNF-α)說明書
人腫瘤壞死因子α(TNF-α)說明書
發(fā)布時(shí)間:2016/5/16   點(diǎn)擊次數(shù):4798次

 

Human TNF-α

 

FOR RESEARCH USE ONLY

 

 

Assay range20 ng/L -400 ng/L 96 DETERMINATIONS

 

Purpose

 

This kit allows for the determination of TNF-α concentrations in Human serum.

 

 

Principle of the assay

 

The kit assay Human TNF-α level in the sample, use Purified Human TNF-α antibody to coat microtiter plate wells, make solid-phase antibody, then add TNF-α to wells, Combined TNF-α antibody which With HRP labeled, 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 Human TNF-α in the samples is then determined by comparing the O.D. of the samples to the standard curve.

 

Materials provided with the kit

 

1

washsolution

20ml×1bottle

7

Stop Solution

6ml×1 bottle

 

 

 

 

 

 

2

HRP-Conjugate reagent

6ml×1 bottle

8

Standard800ng/L

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

2

membrane

 

 

 

 

 

6

Chromogen Solution B

6ml×1 bottle

12

Sealed bags

1

 

 

 

 

 

 

 

Specimen requirements

 

  • 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.

 

1

 

 

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:

 

400ng/L

5

Standard

150µl Original density Standard+150µl Standard diluent

 

 

 

 

 

200ng/L

4

Standard

150µl 5 Standard+150µl Standard diluent

 

 

 

 

 

100ng/L

3

Standard

150µl 4 Standard+150µl Standard diluent

 

 

 

 

 

50ng/L

2

Standard

150µl 3 Standard +150µl Standard diluent

 

 

 

 

 

25ng/L

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(or 20-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 10 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

 

 

 

 

2

 

 

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 10 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,

 

3

 

 

the result is the sample actual density.

 

Important notes

 

  • 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.

 

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

 

  • 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 .

 

  • 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.

 

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

 

  • The substrate evade the light preservation.

 

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

 

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

 

  • Do not mix reagents with those from other lots.

 

 

 

Storage and validity

 

1Storage 2-8.

 

2validity six months

 

 

 

 

 

 

 

 

 

 

 

4

 

Human TNF-α

 

FOR RESEARCH USE ONLY

 

 

Assay range20 ng/L -400 ng/L 96 DETERMINATIONS

 

Purpose

 

This kit allows for the determination of TNF-α concentrations in Human serum.

 

 

Principle of the assay

 

The kit assay Human TNF-α level in the sample, use Purified Human TNF-α antibody to coat microtiter plate wells, make solid-phase antibody, then add TNF-α to wells, Combined TNF-α antibody which With HRP labeled, 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 Human TNF-α in the samples is then determined by comparing the O.D. of the samples to the standard curve.

 

Materials provided with the kit

 

1

washsolution

20ml×1bottle

7

Stop Solution

6ml×1 bottle

 

 

 

 

 

 

2

HRP-Conjugate reagent

6ml×1 bottle

8

Standard800ng/L

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

2

membrane

 

 

 

 

 

6

Chromogen Solution B

6ml×1 bottle

12

Sealed bags

1

 

 

 

 

 

 

 

Specimen requirements

 

  • 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.

 

1

 

 

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:

 

400ng/L

5

Standard

150µl Original density Standard+150µl Standard diluent

 

 

 

 

 

200ng/L

4

Standard

150µl 5 Standard+150µl Standard diluent

 

 

 

 

 

100ng/L

3

Standard

150µl 4 Standard+150µl Standard diluent

 

 

 

 

 

50ng/L

2

Standard

150µl 3 Standard +150µl Standard diluent

 

 

 

 

 

25ng/L

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(or 20-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 10 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

 

 

 

 

2

 

 

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 10 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,

 

3

 

 

the result is the sample actual density.

 

Important notes

 

  • 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.

 

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

 

  • 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 .

 

  • 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.

 

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

 

  • The substrate evade the light preservation.

 

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

 

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

 

  • Do not mix reagents with those from other lots.

 

 

 

Storage and validity

 

1Storage 2-8.

 

2validity six months

 

 

 

 

 

 

Human TNF-α

 

FOR RESEARCH USE ONLY

 

 

Assay range20 ng/L -400 ng/L 96 DETERMINATIONS

 

Purpose

 

This kit allows for the determination of TNF-α concentrations in Human serum.

 

 

Principle of the assay

 

The kit assay Human TNF-α level in the sample, use Purified Human TNF-α antibody to coat microtiter plate wells, make solid-phase antibody, then add TNF-α to wells, Combined TNF-α antibody which With HRP labeled, 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 Human TNF-α in the samples is then determined by comparing the O.D. of the samples to the standard curve.

 

Materials provided with the kit

 

1

washsolution

20ml×1bottle

7

Stop Solution

6ml×1 bottle

 

 

 

 

 

 

2

HRP-Conjugate reagent

6ml×1 bottle

8

Standard800ng/L

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

2

membrane

 

 

 

 

 

6

Chromogen Solution B

6ml×1 bottle

12

Sealed bags

1

 

 

 

 

 

 

 

Specimen requirements

 

  • 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.

 

1

 

 

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:

 

400ng/L

5

Standard

150µl Original density Standard+150µl Standard diluent

 

 

 

 

 

200ng/L

4

Standard

150µl 5 Standard+150µl Standard diluent

 

 

 

 

 

100ng/L

3

Standard

150µl 4 Standard+150µl Standard diluent

 

 

 

 

 

50ng/L

2

Standard

150µl 3 Standard +150µl Standard diluent

 

 

 

 

 

25ng/L

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(or 20-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 10 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

 

 

 

 

2

 

 

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 10 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,

 

3

 

 

the result is the sample actual density.

 

Important notes

 

  • 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.

 

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

 

  • 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 .

 

  • 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.

 

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

 

  • The substrate evade the light preservation.

 

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

 

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

 

  • Do not mix reagents with those from other lots.

 

 

 

Storage and validity

 

1Storage 2-8.

 

2validity six months

 

 

 

 

 

 

Human TNF-α

 

FOR RESEARCH USE ONLY

 

 

Assay range20 ng/L -400 ng/L 96 DETERMINATIONS

 

Purpose

 

This kit allows for the determination of TNF-α concentrations in Human serum.

 

 

Principle of the assay

 

The kit assay Human TNF-α level in the sample, use Purified Human TNF-α antibody to coat microtiter plate wells, make solid-phase antibody, then add TNF-α to wells, Combined TNF-α antibody which With HRP labeled, 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 Human TNF-α in the samples is then determined by comparing the O.D. of the samples to the standard curve.

 

Materials provided with the kit

 

1

washsolution

20ml×1bottle

7

Stop Solution

6ml×1 bottle

 

 

 

 

 

 

2

HRP-Conjugate reagent

6ml×1 bottle

8

Standard800ng/L

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

2

membrane

 

 

 

 

 

6

Chromogen Solution B

6ml×1 bottle

12

Sealed bags

1

 

 

 

 

 

 

 

Specimen requirements

 

  • 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.

 

1

 

 

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:

 

400ng/L

5

Standard

150µl Original density Standard+150µl Standard diluent

 

 

 

 

 

200ng/L

4

Standard

150µl 5 Standard+150µl Standard diluent

 

 

 

 

 

100ng/L

3

Standard

150µl 4 Standard+150µl Standard diluent

 

 

 

 

 

50ng/L

2

Standard

150µl 3 Standard +150µl Standard diluent

 

 

 

 

 

25ng/L

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(or 20-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 10 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

 

 

 

 

2

 

 

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 10 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,

 

3

 

 

the result is the sample actual density.

 

Important notes

 

  • 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.

 

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

 

  • 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 .

 

  • 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.

 

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

 

  • The substrate evade the light preservation.

 

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

 

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

 

  • Do not mix reagents with those from other lots.

 

 

 

Storage and validity

 

1Storage 2-8.

 

2validity six

文件下載    圖片下載    
极品偷香村医全文免费阅读| 高潮AAA人人爽人人爱| 亚洲AV久久无码精品九九| 蜜桃成人无码AV在线观看一电影| 亚洲精品乱码久久久久久蜜桃图片| 无码高潮少妇毛多水多水免费| 丰满人妻中伦妇伦精品APP| 精品成A人无码亚洲成A按摩| 扒开老师双腿猛进入白浆小说| 精品无码国产一区二区三区麻豆| 天天摸日日添狠狠添婷婷| 国产精品亚洲日韩欧美色窝窝色欲| 国产69精品久久久久777| 精品久久久久久无码中文野结衣| 免费A级毛片无码免费视频APP| 无码免费人妻A片AAA毛片一区| 久久伊人色AV天堂九九小黄鸭| AAAAA级少妇高潮大片| 久久国产精品无码一区二区三区| 久久午夜羞羞影院免费观看| 国产色视频一区二区三区| 精品一区二区三区免费播放| 羞羞漫画_成人漫画_成人专用| 亚洲一区二区三区日本久久九| 超碰国产精品久久国产精品99| 999久久久免费精品国产| 精品国产一区二区三区四区VR| 曰本性L交片免费看| 粗大黑头紫大黑头紫挤进| CHINESE山西老熟女BBW| H视频在线观看| 老板把我抱到办公室揉我胸视频| 天堂√最新版中文在线| 国产在线精品一区二区中文| 亚洲人成无码网站在线观看| 久久精品99久久香蕉国产色戒| 国产免费一区二区三区免费视频| 高傲人妻女教师的沉沦长篇| 成人免费一区二区三区视频| 美女脱内衣让男生揉摸的视频| 日日摸日日踫夜夜爽无码久久|