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Anti-ESA/FITC熒光素標記ESA抗體IgG(標記抗體)
點擊次數(shù):33發(fā)布時間:2016/7/24 13:50:07

更新日期:2016/7/24 13:50:07
所 在 地:中國大陸
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【Anti-ESA/FITC熒光素標記ESA抗體IgG(標記抗體)】齊一生物專業(yè)代理Sigma西格瑪.美國BD.賽默飛thermofisher.日本wako.TCL.默克Merck .美國AMRESCO.Invitrogen.日本榮研化學株式會社.EP(歐洲藥典).USP(美國藥典).BP(英國藥典)加拿大TRC等試劑.標準品.對照品原裝產(chǎn)品,正品原裝質(zhì)量,貨期短價格優(yōu)惠!歡迎前來選購齊一生物銷售:021-6034 8496;181214 53965;173021 04490網(wǎng)站:http://www.qiyibio.com【Anti-ESA/FITC熒光素標記ESA抗體IgG(標記抗體)】
QT-00110 釀酒酵母ATCC26603 凍干粉
QT-00111 釀酒酵母ATCC26785 凍干粉
QT-00112 運動發(fā)酵單孢菌ATCC29191 凍干粉
QT-00113 假單胞桿菌ATCC31554 凍干粉
QT-00114 糞產(chǎn)堿桿菌ATCC31555 凍干粉
QT-00115 菅囊酵母ATCC32691 凍干粉
QT-00116 弗氏檸檬酸桿菌ATCC10787 凍干粉 【Anti-ESA/FITC熒光素標記ESA抗體IgG(標記抗體)】
QT-00117 莢膜紅細菌ATCC11166 凍干粉
QT-00118 發(fā)根土壤桿菌(發(fā)根植物單胞菌)ATCC11325 凍干粉
QT-00119 生孢梭菌(產(chǎn)芽孢梭狀芽孢桿菌)ATCC11437 凍干粉
QT-00120 痤瘡丙酸桿菌ATCC11827 凍干粉
QT-00121 地衣芽孢桿菌ATCC11946 凍干粉
QT-00122 谷氨酸棒桿菌ATCC13032 凍干粉
QT-00123 熏衣草灰鏈霉菌ATCC13306 凍干粉
QT-00124 豬霍亂沙門氏菌豬霍亂亞種ATCC13312 凍干粉
QT-00125 脫氮假單胞菌ATCC13867 凍干粉
QT-00126 耐放射異常球菌ATCC13939 凍干粉
QT-00127 綠針假單胞菌ATCC13985 凍干粉
QT-00128 腸炎沙門氏菌腸炎亞種ATCC14028 凍干粉
QT-00129 巨大芽孢桿菌ATCC14581 凍干粉
QT-00130 吸水鏈霉菌奧薩霉素亞種ATCC15420 凍干粉
QT-00131 長雙歧桿菌ATCC15707 凍干粉
QT-00132 放射性根瘤菌ATCC15955 凍干粉 【Anti-ESA/FITC熒光素標記ESA抗體IgG(標記抗體)】
QT-00133 短密青霉ATCC16024 凍干粉
QT-00134 副溶血性弧菌ATCC17802 凍干粉
QT-00135 單核增生李斯特菌ATCC19115 凍干粉
QT-00136 缺陷短波單胞菌ATCC19146 凍干粉
QT-00137 師崗鏈霉菌ATCC19166 凍干粉
QT-00138 脫氮付球菌ATCC19367 凍干粉
QT-00139 絲狀鏈霉菌ATCC19753 凍干粉
QT-00140 裂殖壺菌ATCC20888 凍干粉
QT-00141 產(chǎn)朊假絲酵母ATCC22023 凍干粉
9237378 BR MDx, Installation The Installation, BR MDx facilitates the quick implementation of the BioRobot MDx into the lab routine by minimizing the instrument start-up phase. It covers the hardware and software installation of the BioRobot MDx instrument and provides the user with an introductory training on operation and user maintenance. The installation includes labor and travel costs. The performance of the installation process is documented on a GMP/GLP-compliant Field Service document. CNY
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9243654 Comprehen Valid., Other Quant. 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). 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
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