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齐一生物专业代理Sigma西格玛.美国BD.赛默飞thermofisher.日本wako.TCL.默克Merck .美国AMRESCO.Invitrogen.日本荣研化学株式会社.EP(欧洲药典).USP(美国药典).BP(英国药典)加拿大TRC等试剂.标准品.对照品原装产品,正品原装质量,货期短价格优惠!欢迎前来选购【羧肽酶A(牛胰)CAS:11075-17-5】齐一生物科技(上海)有限公司客服热:400 9910 197/021-6034 8496网站:http://www.qiyibio.com
羧肽酶A(牛胰)CAS:11075-17-5 英文名称:Carboxypeptidase A 规格:BR,50u/mg 包装:500U 储存条件: 2~8℃
QY-G066 人肺腺癌细胞 H1299 上皮细胞 贴壁 RPMI-1640 胎牛血清 【羧肽酶A(牛胰)CAS:11075-17-5】
QY-G067 人高转移肺癌细胞 95-D 上皮细胞 贴壁 RPMI-1640 小牛血清
QY-G068 人肺癌细胞 H125 上皮细胞 贴壁 RPMI-1640 胎牛血清
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QY-G070 人小细胞肺癌细胞 NCI-H446 上皮细胞 贴壁 RPMI-1640 小牛血清
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QY-G076 人肺腺癌细胞(胸膜渗出液) Calu-3 上皮细胞 贴壁 DMEM(high glucose) 小牛血清
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QY-G081 人结肠癌细胞 HT-29 上皮细胞 贴壁 DMEM(high glucose) 小牛血清
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337620 qBiomarker SYBR Green Fluor Mastermix(2) CNY
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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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