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兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨

點(diǎn)擊次數(shù):14發(fā)布時(shí)間:2016/8/1 20:53:41

兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨

更新日期:2016/8/1 20:53:41

所 在 地:中國大陸

產(chǎn)品型號(hào):

簡單介紹:兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨 QY-R95225 國產(chǎn)/進(jìn)口原裝 48T/96T 齊一生物科技(上海)有限公司銷售:021-6034 8496;181214 53965;173021 04490

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詳細(xì)內(nèi)容

 兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨【友情提示】:本產(chǎn)品僅供科研研究使用,不得用于人體臨床直接檢測。避免給您帶來不必要的損失,請(qǐng)仔細(xì)閱讀購買說明!

 

 

價(jià)格詳細(xì)資料:試劑盒價(jià)格電議,齊一生物銷售:0216034 8496;181214 53965173021 04490,齊一生物科技(上海)有限公司提供ELISA試劑盒受到了廣大研究所.中科院科研單位一致肯定和認(rèn)同。齊一生物大品牌保證,傾力為國內(nèi)外科研院校實(shí)驗(yàn)室提供*優(yōu)質(zhì)產(chǎn)品。

兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨注意事項(xiàng)

1. 當(dāng)混合蛋白溶液時(shí)應(yīng)盡量輕緩,避免起泡。

2. 洗滌過程非常重要,不充分的洗滌易造成假陽性。

3. 一次加樣時(shí)間控制在5分鐘內(nèi),如標(biāo)本數(shù)量多,推薦使用排槍加樣。

4. 請(qǐng)每次測定的同時(shí)做標(biāo)準(zhǔn)曲線,做復(fù)孔。

5. 如標(biāo)本中待測物質(zhì)含量過高,請(qǐng)先稀釋后再測定,計(jì)算時(shí)請(qǐng)*后乘以稀釋倍數(shù)。

6. 在配制標(biāo)準(zhǔn)品、檢測溶液工作液時(shí),請(qǐng)以相應(yīng)的稀釋液配制,不能混淆。

7. 底物請(qǐng)避光保存。

8. 不要用其它生產(chǎn)廠家的試劑替換試劑盒中的試劑。

FOR RESEARCH USE ONLY

Drug Names

Generic Name

This kit can be used for determination of serum, plasma and liquid samples Organization Content.

The experimental principle:

The product levels were measured in samples of the kit by double antibody sandwichmethod. The product with the purified antibody coated microtiter plate, made of solid phase antibody, to package is the product antigen monoclonal antibodies are then added to the micropores, the product and then with HRP labeled antibody binding, the formation of antibody - antigen - antibody complex enzyme label, after thorough washing with TMB chromogenic substrate. TMB in the HRP enzyme catalytic conversion into the blue, and in the action of acid into the final yellow. This product is positively related to the depth of color and in the samples. Instrument measured absorbance in the 450nm wavelength with ELISA (OD), the product concentration in the samples was calculated by standard curve.

Materials provided with the kit

 

Materials provided with the kit 96 determinations Storage

User manual   1  

Closure plate membrane   2  

Sealed bags   1  

Microelisa stripplate    1   2-8

Standard360ng/L 0.5ml×1 bottle   2-8

Standard diluent  1.5ml×1 bottle   2-8

HRP-Conjugate reagent    6ml×1 bottle 2-8

Sample diluent    6ml×1 bottle 2-8

Chromogen Solution A 6ml×1 bottle 2-8

Chromogen Solution B 6ml×1 bottle 2-8

Stop Solution 6ml×1 bottle 2-8

wash  solution    20ml×30 fold

×1bottle  2-8

Specimen requirements

1.    serum- coagulation at room temperature 10-20 mins,centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again. 兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨

2.    plasma-use suited EDTA or citrate plasma as an anticoagulant,mix 10-20 mins ,centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again.

3.    Urine-collect sue a sterile container, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again. The Operation of Hydrothorax and cerebrospinal fluid Reference to it.

4.    cell culture supernatant-detect secretory components, collect sue a sterile container, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant,detect the composition of cells, Dilut cell suspension with PBSPH7.2-7.4, Cell concentration reached 1 million / ml, repeated freeze-thaw cycles, damage cells and release of intracellular components, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again.

5.    Tissue samples- After cutting samples, check the weight,add PBSPH7.2-7.4, Rapidly frozen with liquid nitrogen, maintain samples at 2-8 after melting,add PBSPH7.4, Homogenized by hand or Grinders, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant.

6.    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 cant, specimen can be kept in -20 to preserve, Avoid repeated freeze-thaw cycles.

7.    Cant detect the sample which contain NaN3, because NaN3 inhibits HRP active.

Assay procedure

1.Dilute and add sample to Standard: set 10 Standard wells on the ELISA plates coated, add Standard 100μl to the first and the second well, then add Standard dilution 50μl to the first and the second well, mix; take out 100μl form the first and the second well then add it to the third and the forth well separately. then add Standard dilution 50μl to the third and the forth well ,mix ; then take out 50μl from the third and the forth well discard, add 50μl to the fifth and the sixth well ,then add Standard dilution 50μl to the fifth and the sixth well, mix ; take out 50μl from the fifth and the sixth well and add to the seventh and the eighth well, then add Standard dilution 50μl to the seventh and the eighth well ,mix ; take out 50μl from the seventh and the eighth well and add to the ninth and the tenth well, add Standard dilution 50μl to the ninth and the tenth well, mix , take out 50μl from the ninth and the tenth well discard(add Sample 50μl to each well after Diluting ,(density: 240ng/L,160ng/L ,80ng/L,40ng/L, 20ng/L)

2.add sampleSet blank wells separately (blank comparison wells .dont 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 , dont touch the well wall as far as possible, and Gently mix. 兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨

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 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.

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 mins, if the number of sample is much , recommend to use Volley . 兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨

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.

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.

 

 

Storage and validity

1Storage  2-8.

2validity six months.

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Service response time (repair): 5 business days

Periodic inspection/maintenance: not included

Inspection/maintenance delivery: not applicable

Cost coverage for Repair Parts : yes, full coverage

Cost coverage for labor: yes, full coverage

Cost coverage for travel: yes, full coverage

Replacement system (Loaner) provision: not applicable

Transportation cost coverage: not applicable"        CNY                             

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9019464  UV tube, Cxx             CNY                             

9243650  Comprehen Valid., EZ1/QIAcube/QIAsymph    """The Comprehensive Validation Support plan specific to a laboratory's needs will incorporate all of the requirements for the internal validation guidelines from the FBI's Quality Assurance Standards (QAS).

 

The Comprehensive Validation Support service includes all travel and labor charges for up to 20 days by the QIAGEN Validation Team. Typically, one week will be required to extract, quantify, and amplify the validation study samples and may require multiple individuals. Usually, two weeks is required to analyze the data and one week to write the final report. The expected time period to complete the Comprehensive Validation is six weeks. The actual time may vary depending on resource availability, including laboratory time dedicated to validation activities.

 

Lab Work – The QIAGEN specialist(s) will travel to the laboratory to conduct the on-site validation lab work. The QIAGEN specialist team will perform and complete all extractions, quantifications, amplfications, and capillary electrophoresis. The laboratory is responsible for providing systems/protocols that may be needed (generally laboratory SOPs, ex. interpretation guidelines). Additionally, the laboratory staff may be required to provide additional data needed for interpretation (ex. quantification/amplification/CE results) during the data review phase of the validation.

 

Once the final scope of the validation is determined, QIAGEN will provide a quote for all consumables required for the validation.  Non-QIAGEN chemistry and accessories are not included and should  be purchased to cover the validation experimental design including qPCR, STR, NIST standards, required samples types (blood, semen, buccal samples) and required substrates (swabs, materials, etc).   The Customer is expected to have all materials on-hand 1 week prior to the validation start date.

 

Data Analysis – The Comprehensive Validation Support plan encompasses data collection (quants, amps, CE) during the on-site visit. The laboratory may be responsible for sharing (typically electronically via e-mail) any validation data requested after the on-site visit. A QIAGEN specialist will complete all of the data analysis produced from the validation study design. This includes qPCR (quant) and STR (amp) analysis and linkage to starting samples.

 

Validation data CD/flashdrive – QIAGEN will review the validation data and draft a validation summary document, ensuring compliance with the FBI's QAS requirements/standards. QIAGEN will send validation data in an electronic format (email/CD/flashdrive) to the laboratory. The laboratory is responsible for final compilation, any format change preferences, review and signoff of the validation report. The documentation provided by QIAGEN will aide in demonstrating compliance with all accreditation guidelines during laboratory audits. Should a hard copy of the validation study be preferred, the laboratory is required to specify prior to the onset of the validation.

 

Post-validation QIAGEN-to-Laboratory Transfer – Following completion of the validation and generation of the draft validation summary document, a designated member of the QIAGEN validation team will review the validation with the Lab Manager and the Technical Leader. Following sign off on the validation report, training of the laboratory DNA staff will occur. Refer to the Post-validation Competency Training for additional information. """     CNY                             

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9237155  V-Housing with Sample Needle                  CNY                             

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9011882  Back unit, BR9600            CNY                             

9011823  Z-Modul; Tip-Adapter 300µl; BR8000               CNY                             

9236916  3 Year Warranty, LiquiChip       LiquiChip 3-year Warranty with 1 Preventive Maintenance per year.  Included in system price.  This warranty must be included as a line item on the system quote.  It covers the system for three years total including all per incident travel and labor charges, all repair parts, one preventive maintenance visits per year (three in total), and 48- hour priority response.     CNY                             

9019143  Power supply, PyroQ96             CNY                             

9019129  Cable - Reagent, PyroQ96ID             CNY                             

9019126  PCB 2 - Connection, PyroQ96ID                 CNY                             

9019114  IPC mainboard, PyroQ96ID               CNY                             

9019025  Worktable, side wall, left, EZ1xl                CNY                             

9019012  Motor Y, EZ1xl          CNY                             

9018942  Adapter, 2xRing of 12 COBAS Amplicore          CNY                             

9022737  Rotor-Gene AssayManager SOW              CNY                             

9016061  Tubing Set, Syringe inlet, BR8000 I           CNY                             

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QY-L0802 石杉?jí)A甲102518-79-6   (-)-Huperzine A         102518-79-6    20mg                          

QY-L0803 石杉?jí)A乙(95%103548-82-9      Huperzine B     103548-82-9    20mg                          

QY-L0804 3,4,5-三甲氧基苯甲酸甲酯1916-07-0  Methyl 3,4,5-trimethoxybenzoate  1916-07-0         20mg                         

QY-L0805 3,4,5-三甲氧基苯甲酸118-41-2    Gallic acid trimethyl ether       118-41-2  20mg                          

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QY-L0809 石吊蘭素152743-19-6   Lysionotin          152743-19-6    20mg                          

QY-L0810 麝香酮541-91-3      3-Methylcyclopentadeca          541-91-3  20mg                          

QY-L0811 酮麝香81-14-1        "Musk ketone

"       81-14-1    20mg                           【兔子巨噬細(xì)胞炎性蛋白1α(MIP-1α/CCL3)ELISA試劑盒現(xiàn)貨】

QY-L0812 桑辛素62596-29-6 Morusin   62596-29-6       20mg                          

QY-L0813 桑色素480-16-0      Morin       480-16-0  20mg                          

QY-L0814 桑皮苷A102841-42-9     mulberroside A         102841-42-9    20mg                          

QY-L0815 桑皮苷C102841-43-0      Mulberroside C         102841-43-0    20mg                          

QY-L0816 桑根酮 C 80651-76-9      Sanggenon C    80651-76-9       20mg                          

QY-L0817 桑根酮 D  81422-93-7 Sanggenon D   81422-93-7       20mg                          

QY-L0818 D-松醇10284-63-6 D-Pinitol   10284-63-6       20mg                          

QY-L0819 山姜素36052-37-6 Alpinetin          36052-37-6       20mg                          

QY-L0820 水晶蘭苷5945-50-6        Monotropein   5945-50-6         20mg                          

QY-L0821 鼠李糖6155-35-7   L-Rhamnose monohydrate       6155-35-7         20mg                          

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QY-L0825 酸棗仁皂苷B55466-05-2        Jujuboside B     55466-05-2       20mg                          

QY-L0826 酸棗仁皂苷A1194851-84-8   Jujuboside A1   194851-84-8    20mg                          

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