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Anti-Bad (BCL-xL/BCL-2-associated death promoter)相關(guān)死亡促進(jìn)因子Bad
點(diǎn)擊次數(shù):13發(fā)布時(shí)間:2016/7/18 20:59:42

更新日期:2016/7/18 20:59:42
所 在 地:中國(guó)大陸
產(chǎn)品型號(hào):
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【Anti-Bad (BCL-xL/BCL-2-associated death promoter)相關(guān)死亡促進(jìn)因子Bad抗體】是我公司重點(diǎn)推廣產(chǎn)品,我公司有專業(yè)的人員進(jìn)行全程指導(dǎo),請(qǐng)放心購(gòu)買(mǎi),發(fā)貨時(shí)均會(huì)附上質(zhì)檢報(bào)告單.使用說(shuō)明書(shū)和推薦用法用量,提供正規(guī)發(fā)票. 齊一生物銷售:021-6034 8496;181214 53965;173021 04490網(wǎng)址:www.qiyibio.com
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QY-G154 人子宮內(nèi)膜腺癌細(xì)胞 HEC-1-B 上皮細(xì)胞 貼壁 RPMI-1640 小牛血清
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QY-G157 人宮頸癌細(xì)胞 SiHa 上皮細(xì)胞 貼壁 DMEM(high glucose) 小牛血清 【Anti-Bad (BCL-xL/BCL-2-associated death promoter)相關(guān)死亡促進(jìn)因子Bad抗體】
QY-G158 人宮頸癌細(xì)胞 C-33A 上皮細(xì)胞 貼壁 RPMI-1640 胎牛血清
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QY-G170 人腎癌細(xì)胞 OS-RC-2 上皮細(xì)胞 貼壁 RPMI-1640 小牛血清
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QY-G174 人神經(jīng)膠質(zhì)瘤細(xì)胞 CRT 成纖維細(xì)胞樣 貼壁 DMEM(high glucose) 小牛血清
QY-G175 人膠質(zhì)母細(xì)胞瘤細(xì)胞 A172 成纖維細(xì)胞樣 貼壁 DMEM(high glucose) 小牛血清
QY-G176 神經(jīng)膠質(zhì)瘤細(xì)胞 SHG-44 成纖維細(xì)胞樣 貼壁 RPMI-1640 小牛血清 【Anti-Bad (BCL-xL/BCL-2-associated death promoter)相關(guān)死亡促進(jìn)因子Bad抗體】
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QY-G179 人腎上腺神經(jīng)母細(xì)胞瘤細(xì)胞(腦轉(zhuǎn)移) KP-N-NS 上皮細(xì)胞 貼壁 RPMI-1640 小牛血清
QY-G180 人神經(jīng)上皮瘤細(xì)胞 SK-N-MC 上皮細(xì)胞 貼壁 DMEM(high glucose) 小牛血清
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9243653 Comprehen Valid., Other Extraction Sys """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
386516 Investigator STR GO! Lysis Buffer (200) CNY
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