產(chǎn)品展示
人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家
點(diǎn)擊次數(shù):13發(fā)布時(shí)間:2016/8/15 17:05:15

更新日期:2016/8/15 17:05:15
所 在 地:中國(guó)大陸
產(chǎn)品型號(hào):
優(yōu)質(zhì)供應(yīng)
詳細(xì)內(nèi)容
規(guī)格:小規(guī)格48T.大規(guī)格96T
樣本標(biāo)準(zhǔn):血清,血漿,尿液,胸腹水,腦脊液,細(xì)胞培養(yǎng)上清,組織勻漿等
檢測(cè)方法:酶聯(lián)免疫分析(ELISA)
運(yùn)輸保存:2~8°貯存.保質(zhì)期:6個(gè)月
試驗(yàn)所需自備物品:
1. 酶標(biāo)儀(450nm 波長(zhǎng)濾光片)
2. 高精度移液器,EP 管及一次性吸頭
3. 37℃恒溫箱,雙蒸水或去離子水
4. 吸水紙
【人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家】齊一生物主要經(jīng)營(yíng)進(jìn)口原裝Elisa試劑盒,檢測(cè)試劑種類齊全,價(jià)格實(shí)惠!購(gòu)買齊一生物產(chǎn)品的新老客戶都可享免費(fèi)代測(cè)實(shí)驗(yàn)服務(wù),全程提供技術(shù)支持.如需其它Elisa試劑盒說(shuō)明書(shū)及產(chǎn)品價(jià)格,可來(lái)電咨詢齊一生物銷售:021-6034 8496;181214 53965;173021 04490
試劑盒特點(diǎn)
一、高效、靈敏、特異的抗體;
二、穩(wěn)定的重復(fù)性和可靠性;
三、吸附性能好,空白值低,孔底透明度高的固相載體;
四、適用血清、血漿、組織勻漿液、細(xì)胞培養(yǎng)上清液、尿液等等多種標(biāo)本類型;
試劑盒可概括四個(gè)方面:
1、免疫酶染色各種細(xì)胞內(nèi)成份的定位.
2、研究抗酶抗體的合成.
3、顯現(xiàn)微量的免疫沉淀反應(yīng).
4、定量檢測(cè)體液中抗原或抗體成份.
【人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家】ELISA試劑盒為您節(jié)省實(shí)驗(yàn)經(jīng)費(fèi).
elisa試劑盒回收率是反應(yīng)待測(cè)物在樣品分析過(guò)程中的損失的程度,損失越少,回收率越高,如果作標(biāo)液1PPM,就是1毫克/升,而作出標(biāo)準(zhǔn)數(shù)據(jù)為0.99毫克/升,就是說(shuō)你的回收率是99%,這個(gè)與真實(shí)成分有密切的關(guān)系,說(shuō)明方法的準(zhǔn)確度.比如水中總無(wú)機(jī)氯含量測(cè)定,樣品水中含有無(wú)機(jī)氯20mg/L,取100mL被測(cè)水樣品,加入0.1mL濃度為10mg/mL的含無(wú)機(jī)氯標(biāo)準(zhǔn)樣品,測(cè)定時(shí)忽略體積變化,如果測(cè)定出樣品中無(wú)機(jī)氯為2.98mg/L,則認(rèn)為回收率為99%.
【人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家】試劑盒制備方法包括以下步驟:
1)抗原表位的計(jì)算機(jī)篩選;
2)抗原的制備;
3)血清的采集;
4)間接ELISA方法的建立;
5)間接ELISA方法的敏感性和特異性驗(yàn)證;
6)試劑盒的穩(wěn)定性驗(yàn)證;
7)對(duì)大量樣本進(jìn)行檢測(cè).該方法簡(jiǎn)單、快速、靈敏度高、特異性強(qiáng)、穩(wěn)定性合格、重復(fù)性好.應(yīng)用本發(fā)明制得的試劑盒能有效檢出樣本含量.適用于大批量樣本的檢測(cè)
試劑盒安全性提示:
1.工作人員實(shí)驗(yàn)中避免直接接觸終止液和底物A、B。一旦接觸到這些液體,請(qǐng)盡快用水沖洗。
2.實(shí)驗(yàn)中不要吃喝、抽煙或使用化妝品。
3.不要用嘴吸取試劑盒里的任何成份。
【人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家】齊一生物【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(cè)。避免給您帶來(lái)不必要的損失,請(qǐng)仔細(xì)閱讀購(gòu)買說(shuō)明!
腎系膜細(xì)胞 5 ×105 1ml
膀胱上皮細(xì)胞 5 × 105 1ml
膀胱平滑肌細(xì)胞 5 × 105 1ml
腎動(dòng)脈內(nèi)皮細(xì)胞 5 × 105 1ml
腎動(dòng)脈平滑肌細(xì)胞 5 × 105 1ml
腎小管上皮細(xì)胞 5 × 105 1ml
骨細(xì)胞 5 × 105 1ml
滑膜細(xì)胞 5 × 105 1ml
骨骼肌細(xì)胞 5 × 105 1ml
表皮角化細(xì)胞 5 × 105 1ml
真皮成纖維細(xì)胞 5 × 105 1ml
軟骨細(xì)胞 5 × 105 1ml
成骨細(xì)胞 5 × 105 1ml
破骨細(xì)胞 5 × 105 1ml
腦動(dòng)脈血管內(nèi)皮細(xì)胞 5 × 105 1ml 【人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家】
腦靜脈血管平滑肌細(xì)胞 5 × 105 1ml
腦靜脈血管內(nèi)皮細(xì)胞 5 × 105 1ml
腦動(dòng)脈血管平滑肌細(xì)胞 5 × 105 1ml
腦膜細(xì)胞 5 × 105 1ml
神經(jīng)元細(xì)胞 5 × 105 1ml
神經(jīng)膠質(zhì)細(xì)胞 5 × 105 1ml
腦微血管內(nèi)皮細(xì)胞 5 × 105 1ml
眼晶狀體上皮細(xì)胞 5 × 105 1ml
視網(wǎng)膜微血管內(nèi)皮細(xì)胞 5 × 105 1ml
小梁網(wǎng)細(xì)胞 5 × 105 1ml
視網(wǎng)膜色素上皮細(xì)胞 5 × 105 1ml
視網(wǎng)膜muller細(xì)胞 5 × 105 1ml
虹膜色素上皮細(xì)胞 5 × 105 1ml
角膜上皮細(xì)胞 5 × 105 1ml
角膜內(nèi)皮細(xì)胞 5 × 105 1ml
胰島β細(xì)胞 5 × 105 1ml 【人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家】
5128-1220 Specimen Transport Medium (STM) CE CNY
5123-1220 Female Swab Specimen Collection KitTM CNY
5100-1400IVD hc2 Sample Conversion Kit CNY
EA11424 EASYartus BKV RG_II CNY
5050-1075 V.1 CD Rom Manual, MST Vortexer 2 CNY
EA10124 EASYartus EBV RG PCR Kit 2 CNY
BR-02 DxS B-RAF Mutation Test Kit CNY
9240729 Tubing, 3/8"OD , Red, AP CNY
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9240701 O-Ring, Shaker, Lower Body, AP96/196 CNY 【人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家】
9240696 Fitting, Barbed, 1/4" ID tube, AP CNY
9243651 Comprehen Valid., QIAgility """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). For planning purposes and to ensure a smooth process, the Customer is expected to have all materials on-hand and inventoried one (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
218076 miScript SYBR Green PCR Kit (2000) CNY
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280437 virotype BTV RT-PCR Kit (480) CNY
932836 #QIAsymphony Ni-NTA Denat. Kit (384) CNY
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9238243 ZLV BioRobot M96 User Manual CNY
9019988 ZLV Mainboard, QGY CNY
9020553 Foam angle, transport box, QIAC CNY
9020582 X-Motor, DML3000 CNY
9020584 Y-Belt, DML3000 320 Teeth CNY
9020594 Enclosure, DML3000 CNY
9021006 Motor, Pipettor Y, DCU CNY
9236333 Sample Loop CNY 【人鈣粘蛋白相關(guān)的神經(jīng)受體1(CNR-1)ELISA試劑盒廠家】
9013382 Shaker adapter, microplate, LHS CNY
9013275 Motor, gripper, handler T/L, BR3000 CNY
9013269 Fitting, PA tubing M6x1, 2.25mm, (10) CNY
9013210 Cabling kit, moving, BR8000 CNY
9013198 Tubing,pres.sen.con.auto vac,BR8000v1.00 CNY
9013188 Valve set, pressure relaese, dispenser, CNY
9011730 Cable, level sensor, BR8000 CNY