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人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家
點擊次數(shù):12發(fā)布時間:2016/8/17 15:07:53

更新日期:2016/8/17 15:07:53
所 在 地:中國大陸
產(chǎn)品型號:
優(yōu)質(zhì)供應
詳細內(nèi)容
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價格詳細資料:試劑盒價格電議,齊一生物銷售:021-6034 8496;181214 53965;173021 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同。齊一生物大品牌保證,傾力為國內(nèi)外科研院校實驗室提供*優(yōu)質(zhì)產(chǎn)品。
【人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家】注意事項
1. 當混合蛋白溶液時應盡量輕緩,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. 一次加樣時間控制在5分鐘內(nèi),如標本數(shù)量多,推薦使用排槍加樣。
4. 請每次測定的同時做標準曲線,做復孔。
5. 如標本中待測物質(zhì)含量過高,請先稀釋后再測定,計算時請*后乘以稀釋倍數(shù)。
6. 在配制標準品、檢測溶液工作液時,請以相應的稀釋液配制,不能混淆。
7. 底物請避光保存。
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℃
Standard:360ng/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. 【人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家】
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 PBS(PH7.2-7.4), 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 PBS(PH7.2-7.4), Rapidly frozen with liquid nitrogen, maintain samples at 2-8℃ after melting,add PBS(PH7.4), 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 can’t, specimen can be kept in -20 ℃ to preserve, Avoid repeated freeze-thaw cycles.
7. Can’t 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 sample:Set blank wells separately (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. 【人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家】
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.washing:Uncover 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 enzyme:Add HRP-Conjugate reagent 50μl to each well, except blank well.
7.incubate:Operation with 3.
8.washing:Operation with 5.
9.color:Add Chromogen Solution A 50ul and Chromogen Solution B to each well, evade the light preservation for 15 min at 37℃
10.Stop the reaction:Add Stop Solution50μl to each well, Stop the reaction(the blue color change to yellow color).
11.assay:take 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 . 【人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家】
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.
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Storage and validity
1.Storage: 2-8℃.
2.validity: six months.
9011892 Tubing, teflon, M6, 2.5 x 0.5 mm, 0.65 m CNY
9011887 Holder, tip rack, front unit CNY
9011881 Front unit, BR9600 CNY
9011878 Shaker adapter, microplate Adapter for accommodating four 96-well plates or othe labware with the same base dimensions) on the 4-plate shaker system; not for use with the robotic handling system CNY
9011862 Worktable right, BR8000 v1.01 CNY
9019147 IPC Hard Drive - no software, PyroQ96 CNY
9019072 PyroMark Plate Hotel, PyroQ96MD CNY
9019062 PyroMark Q24 Software For use with PyroMark Q24 instrument.Software for setting up a run and analyzing mutations and CpGs CNY
9019000 Cover, rear, EZ1xl CNY
9018998 Cover, front, top, EZ1xl CNY
9018956 Reagent Block, 24x2ml Flat-Base Tubes CNY
9018945 Adapter QIAGEN BioRobot M48 Tubes CNY
9022706 Clevis Pin, X-pulley, DML3000 CNY
9016062 Tubing Set, Wash pump, BR8000 I CNY
9016031 Tubing, retractable, DISU, BR8 RD v2 CNY 【人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家】
9015712 DISU Retraction Mechanism BR8,complete CNY
9015654 Communication cable RS485, BR M48 CNY
9015594 PM Kit Biorobot EZ1 CNY
9019160 Valve - Dispense, PyroQ96MD CNY
9014206 Tubing Set, Waste Sys., BR8 RD CNY
9014139 Sensor; 4l-Bottle; Vac.-Cont.; BR8000 CNY
9014118 Tubing, vacuum, textile reinforced, 3m CNY
9014061 Magnet, 96-well, Type A CNY
9021199 Transport Box PyroMark Q24 CNY
9021163 QIAxcel ScreenGel Software CNY
35370 Penta-His Alexa Fluor 647 Conjugate 125 ul Penta-His Alexa Fluor 647 Conjugate, 200 ug/ml CNY
9018300 EZ1 Advanced Test Card CNY
9018293 EZ1 Advanced DNA Blood Card CNY
800354 Setup Large Clone / Large Scale /Genomic CNY
9239544 Assy, XY, Slotted Optical Switch 2 CNY
9015287 Filter, dust, left, M48 CNY 【人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家】
QM101-6 Pfu DNA Polymerase(2.5u/ul) 250U
QM101-8 long taq DNA Polymerase(2.5u/ul) 250U
QM101-9 冷抑制熱啟動HotStart Taq DNA Polymerase 250U
QM101-09 2×HotStart Taq PCR MasterMix(含染料) 0.5ml
QM101-12 10x JumpStart Buffer 熱啟動緩沖液(不含酶) 1ML
QM101-14 2 x SY Green qPCR Mix 50200
QM201-1 2×Taq PCR MasterMix(含染料) 1ml5×1ml
QM201-3 2×Taq PCR MasterMix(不含染料) 1ml5×1ml
QM201-5 2×Taq Plus PCR MasterMix(含染料) 0.5ml5×1ml
QM201-7 2×Taq Plus PCR MasterMix(不含染料) 0.5ml5×1ml 【人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家】
QM201-9 2×Pfu PCR MasterMix(含染料) 0.5ml5×1ml
QM201-11 2×Pfu PCR MasterMix(不含染料) 0.5ml5×1ml
QM201-13 2×Long Taq PCR Master Mix(含染料) 0.5m
QM201-15 2×Long Taq PCR Master Mix(不含染料) 0.5m
QM201-17 2×HotStart Taq PCR MasterMix(含染料) 0.5m
QM201-19 2×HotStart Taq PCR MasterMix(不含染料) 0.5m
QM301-1 超純 dNTP Mixture(2.5 mM each) 1ML
QM301-4 超純 dNTP Mixture(10 mM each) 1ML
QM301-5 dATP 100mMsolution 0.25 ml
QM301-6 dCTP 100mM solution 0.25 ml
QM301-7 dGTP 100mM solution 0.25 ml
QM301-8 dTTP 100mM solution 0.25 ml
QM301-9 PCR enhancer 100μ
QT101-4 TUREscript 1st Strand cDNA Synthesis Kit(鏈反轉(zhuǎn)錄試劑盒) 2050
QT101-1 TUREscript H Minus M-MuLV Reverse Transcriptase 5000U
QT101-6 TUREscript One Step RT-PCR Kit(一步法反轉(zhuǎn)錄試劑盒) 2050 【人T細胞活化連接蛋白(LAT)ELISA試劑盒廠家】
QT101-8 TUREscript SY Green qRT-PCR Kit (兩步法熒光定量反轉(zhuǎn)錄試劑盒) 2050
QD101-1 DNA MarkerⅠ(條帶100.200.300.400.500.600) "50T
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QD101-3 DNA Marker Ⅱ(條帶100.300.500.700.900.1200) "50T
"
QD101-5 DNA Marker Ⅲ(條帶300.500.800.1500.2000.3000.5000) "50T
"
QD101-7 DNA Marker Ⅳ(條帶500.1000.1500.3000.5000.8000) "50T
"
QD101-9 DNA Marker Ⅴ(條帶200.400.700.1000.1500.2000) "50T
"
QD101-11 DNA MarkerⅥ(條帶250.1000.2500.5000.7000.10000) "50T
"