欧美三级欧美成人高清,麻豆网神马久久人鬼片,男同gay自慰网站,欧美日韩精品一区二区三区激情,在线,男人的天堂av

您的位置:易推廣 > 化工原料 > 化學(xué)試劑 > 生化試劑 > 齊一生物科技(上海)有限公司 > 產(chǎn)品展示 > ELISA檢測(cè)試劑盒 > 雞源ELISA試劑盒 > 雞網(wǎng)狀內(nèi)皮增生癥(ChickenREV)ELISA試劑盒

產(chǎn)品展示

雞網(wǎng)狀內(nèi)皮增生癥(ChickenREV)ELISA試劑盒

點(diǎn)擊次數(shù):25發(fā)布時(shí)間:2016/6/2 18:05:57

雞網(wǎng)狀內(nèi)皮增生癥(ChickenREV)ELISA試劑盒

更新日期:2016/8/27 11:11:43

所 在 地:中國大陸

產(chǎn)品型號(hào):

簡(jiǎn)單介紹:雞網(wǎng)狀內(nèi)皮增生癥(ChickenREV)ELISA試劑盒 貨號(hào)QY-C60096 48T/96T 品牌QYBIO 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 elisa酶聯(lián)免疫分析法 詳細(xì)請(qǐng)見說明書 科研檢測(cè)

優(yōu)質(zhì)供應(yīng)

詳細(xì)內(nèi)容

 雞網(wǎng)狀內(nèi)皮增生癥(ChickenREV)ELISA試劑盒規(guī)    格:96T/48T

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)原理:ELISA試劑盒采用雙抗體一步夾心法酶聯(lián)免疫吸附試驗(yàn)(ELISA

試劑盒保存:2-8℃。

有效期:6個(gè)月

運(yùn)輸方法:泡沫箱配生物冰袋運(yùn)輸

 

雞網(wǎng)狀內(nèi)皮增生癥(ChickenREV)ELISA試劑盒提供免費(fèi)代測(cè)的服務(wù):(您只需把標(biāo)本寄過來,我們?yōu)槟?jié)省時(shí)間,幫您出結(jié)果,原始數(shù)據(jù),分析數(shù)據(jù)均可提供,實(shí)驗(yàn)時(shí)間五個(gè)工作日給您結(jié)果.)如有什么問題請(qǐng)給我們來電:齊一生物銷售:0216034 8496;181214 53965173021 04490;并留下您寶貴的意見和建議、齊一生物全體員工將全心全意為您服務(wù)!產(chǎn)品種類齊全、質(zhì)量可靠、價(jià)格優(yōu)惠、靈敏度高、效果穩(wěn)定、易保存、操作簡(jiǎn)單雞網(wǎng)狀內(nèi)皮增生癥(ChickenREV)ELISA試劑盒

 

QYS-03059二胺氧化酶測(cè)試盒50管/24樣可見分光光度法

QYS-03060超氧陰離子測(cè)試盒50管/24樣可見分光光度法

QYS-03061超氧化物歧化酶SOD測(cè)試盒50管/48樣可見分光光度法

QYS-03062超氧化物歧化酶SOD測(cè)試盒100管/96樣酶標(biāo)法

QYS-03063過氧化氫酶CAT測(cè)試盒50管/48樣紫外分光光度法

QYS-03064過氧化物酶POD測(cè)試盒50管/48樣可見分光光度法

QYS-03065銅藍(lán)蛋白含量測(cè)試盒50管/24樣可見分光光度法

QYS-03066銅藍(lán)蛋白含量測(cè)試盒100管/48樣酶標(biāo)法

QYS-03067總抗氧化能力T-AOC測(cè)試盒50管/48樣可見分光光度法

QYS-03068總抗氧化能力T-AOC測(cè)試盒100管/96樣酶標(biāo)法

QYS-03069羥自由基清除能力測(cè)試盒50管/48樣可見分光光度法

QYS-03070羥自由基清除能力測(cè)試盒100管/96樣酶標(biāo)法

QYS-03071植物類黃酮測(cè)試盒50管/24樣可見分光光度法

QYS-03072植物類黃酮測(cè)試盒100管/48樣酶標(biāo)法

QYS-03073植物總酚測(cè)試盒50管/24樣可見分光光度法

QYS-03074植物總酚測(cè)試盒100管/48樣酶標(biāo)法

QYS-03075植物原花青素測(cè)試盒50管/24樣可見分光光度法

QYS-03076植物原花青素測(cè)試盒100管/48樣酶標(biāo)法

QYS-03077尿酸含量測(cè)試盒50管/24樣可見分光光度法

QYS-03078硫氧還蛋白過氧化物酶TPX測(cè)試盒50管/48樣紫外分光光度法

QYS-03079谷胱甘肽過氧化物酶GPX測(cè)試盒50管/48樣GR法

QYS-03080谷胱甘肽S-轉(zhuǎn)移酶GST測(cè)試盒50管/48樣紫外分光光度法

QYS-03081抗壞血酸AsA含量測(cè)試盒50管/48樣紫外分光光度法

QYS-03082總巰基測(cè)試盒50管/24樣可見分光光度法

QYS-03083總巰基測(cè)試盒100管/48樣酶標(biāo)法

QYS-03084超氧化物歧化酶SOD測(cè)試盒50管/48樣可見分光光度法

QYS-03085超氧化物歧化酶SOD測(cè)試盒100管/96樣酶標(biāo)法

QYS-03086過氧化氫酶CAT測(cè)試盒50管/48樣紫外分光光度法

QYS-03087過氧化物酶POD測(cè)試盒50管/48樣可見分光光度法

 

QYS-03088多酚氧化酶PPO測(cè)試盒50管/24樣可見分光光度法


6000-5000Specimen Collection TubesCNY
5000-1430MST Vortexer II - FoamFeetAssembly, 110VCNY
5128-1220Specimen Transport Medium (STM) CECNY
5123-1220Female Swab Specimen Collection KitTMCNY
5100-1400IVDhc2 Sample Conversion KitCNY
EA11424EASYartus BKV RG_IICNY
5050-1075 V.1CD Rom Manual, MST Vortexer 2CNY
EA10124EASYartus EBV RG PCR Kit 2CNY
BR-02DxS B-RAF Mutation Test KitCNY
9240729Tubing, 3/8"OD , Red, APCNY
9240719Cable Carrier, Capper, Elevator, APCNY
9240701O-Ring, Shaker, Lower Body, AP96/196CNY
9240696Fitting, Barbed, 1/4" ID tube, APCNY
9243651Comprehen 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
218076miScript SYBR Green PCR Kit (2000)CNY
271906cattletype Milk Prep Kit (50)CNY
289980intype IC-DNA (1ml)CNY
280437virotype BTV RT-PCR Kit (480)CNY
932836#QIAsymphony Ni-NTA Denat. Kit (384)CNY
800511Verification Sequencing / DNA productionCNY
9238243ZLV BioRobot M96 User ManualCNY
9019988ZLV Mainboard, QGYCNY
9020553Foam angle, transport box, QIACCNY
9020582X-Motor, DML3000CNY
9020584Y-Belt, DML3000 320 TeethCNY
9020594Enclosure, DML3000CNY
9021006Motor, Pipettor Y, DCUCNY
9236333Sample LoopCNY
9013382Shaker adapter, microplate, LHSCNY
9013275Motor, gripper, handler T/L, BR3000CNY
 

聯(lián)系我們

聯(lián)系人:徐經(jīng)理

點(diǎn)擊查看聯(lián)系方式

企業(yè)檔案

  • 會(huì)員類型:免費(fèi)會(huì)員
  • 工商認(rèn)證: 【已認(rèn)證】
  • 最后認(rèn)證時(shí)間:
  • 法人:
  • 注冊(cè)號(hào):
  • 企業(yè)類型:生產(chǎn)商
  • 注冊(cè)資金:人民幣500萬

script>
在線咨詢

提交