產(chǎn)品展示
AP2關(guān)聯(lián)激酶1抗體
點(diǎn)擊次數(shù):11發(fā)布時(shí)間:2016/7/20 16:33:17

更新日期:2016/7/20 16:33:17
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
【 AP2關(guān)聯(lián)激酶1抗體】齊一生物科技(上海)有限公司檢測(cè)試劑盒產(chǎn)品已被廣泛應(yīng)用于化學(xué)、化工、生命科學(xué)的基礎(chǔ)研究和開(kāi)發(fā)應(yīng)用、制藥、疾病診斷與控制、人口與健康、生物技術(shù)等諸多領(lǐng)域?蛻舯椴紘(guó)內(nèi)各大學(xué)、研究所、醫(yī)院、衛(wèi)生防疫、商品檢驗(yàn)檢疫、制藥公司、生物技術(shù)公司和食品工業(yè)等單位。【 AP2關(guān)聯(lián)激酶1抗體】齊一生物銷售:021-6034 8496;181214 53965;173021 04490網(wǎng)址:www.qiyibio.com
5000-1404 Plate Cartridge 110V, VTX2 CNY
5000-1277 Top Housing W LID, DML2 CNY
5050-1029 Mouse, PC System spare CNY
5025-1011 Expand 4 Pipettor 240V CNY
9240747 Belt, Reagent Pump 117 groove, AP CNY
9240720 Cable Carrier, Tubing, Dispense Head, AP CNY
9240700 Tubing, Waste, 1 1\4", AP CNY
9243690 DML Luminometer, Repair Fee DML Repair Fee covers Regional Repair Center service for non-service agreement covered DML 2000 and DML 3000 units. Includes labor, parts and shipping materials. CNY
9243652 Comprehen Valid., QuantiPlex/QP Hyres """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 AP2關(guān)聯(lián)激酶1抗體
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614033 careHPV Test, SFDA (24-test) CNY
274203 flocktype IBDV Ab (5) CNY
270803 cattletype MAP Ab (5) CNY
280303 cador BVDV RT-PCR Kit (24) CNY
282303 virotype PRRSV RT-PCR Kit (24) CNY
282305 virotype PRRSV RT-PCR Kit (96) CNY
280443 virotype BTV pan/8 RT-PCR Kit (24) CNY
939012 Buffer N2 (2 x 10 ml) CNY
871105 EGFR PCR Kit (100) CNY
800382 Restriction Map CNY
871005 KRAS PCR Kit (100) CNY
9020586 Power Supply, 24V 60W, DML 3000 CNY
9013314 Shaker adapter, 192-tube, 5 ml CNY
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QY-x2372 人胚肺細(xì)胞WI-38
QY-x2373 非洲綠猴腎細(xì)胞Vero
QY-x2374 細(xì)胞淋巴瘤細(xì)胞U-937
QY-x2375 人腦星形膠質(zhì)母細(xì)胞瘤U-87MG
QY-x2376 人膠質(zhì)瘤細(xì)胞U251
QY-x2377 人骨肉瘤細(xì)胞U-2OS
QY-x2378 單核細(xì)胞系THP-1
QY-x2379 人血液白血病細(xì)胞TF-1
QY-x2380 人舌鱗癌細(xì)胞Tca-8113 AP2關(guān)聯(lián)激酶1抗體
QY-x2381 蝙蝠肺細(xì)胞Tb1Lu
QY-x2382 人乳腺管癌細(xì)胞T-47D
QY-x2383 人膀胱移行細(xì)胞癌細(xì)胞T-24
QY-x2384 人結(jié)腸癌細(xì)胞SW620
QY-x2385 人甲狀腺鱗癌細(xì)胞SW579
QY-x2386 人結(jié)腸癌細(xì)胞SW[SW-]
QY-x2387 豬睪丸細(xì)胞系ST
QY-x2388 小鼠骨髓瘤細(xì)胞SP2/0
QY-x2389 人肝癌細(xì)胞SMMC-7721
QY-x2390 人卵巢癌細(xì)胞SK-OV-3
QY-x2391 人肝癌細(xì)胞SK-HEP-1
QY-x2392 人乳腺腺癌細(xì)胞SK-BR-3
QY-x2393 人子宮頸鱗癌細(xì)胞SiHa
QY-x2394 人膠質(zhì)瘤細(xì)胞SHG-44
QY-x2395 人胃癌SGC7901
QY-x2396 人成骨肉瘤細(xì)胞Saos-2
QY-x2397 大鼠雪旺細(xì)胞RSC96
QY-x2398 小鼠前列腺癌細(xì)胞RM-1 AP2關(guān)聯(lián)激酶1抗體
QY-x2399 人結(jié)腸腺癌細(xì)胞RKO
QY-x2400 猴脈絡(luò)膜-視網(wǎng)膜(內(nèi)皮)細(xì)胞RF/6A
QY-x2401 小鼠單核巨噬細(xì)胞白血病細(xì)胞RAW264.7
QY-x2402 人Burkitt's淋巴瘤細(xì)胞Raji