產(chǎn)品展示
聚氧乙烯月桂醚CAS:9002-92-0
點(diǎn)擊次數(shù):10發(fā)布時(shí)間:2016/8/26 21:34:54

更新日期:2016/8/26 21:34:54
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
齊一生物專業(yè)代理Sigma西格瑪.美國(guó)BD.賽默飛thermofisher.日本wako.TCL.默克Merck .美國(guó)AMRESCO.Invitrogen.日本榮研化學(xué)株式會(huì)社.EP(歐洲藥典).USP(美國(guó)藥典).BP(英國(guó)藥典)加拿大TRC等試劑.標(biāo)準(zhǔn)品.對(duì)照品原裝產(chǎn)品,正品原裝質(zhì)量,貨期短價(jià)格優(yōu)惠!歡迎前來(lái)選購(gòu)【聚氧乙烯月桂醚CAS:9002-92-0】齊一生物科技(上海)有限公司客服熱:400 9910 197/021-6034 8496網(wǎng)站:http://www.qiyibio.com
"聚氧乙烯月桂醚CAS:9002-92-0 英文名稱:Brij-35 規(guī)格:高純,有害品 包裝:250克 比重: 0·95
儲(chǔ)存條件: RT
用途: 非離子型去垢劑,用于抽提膜蛋白。典型用量:0·1-1%· 適合用于Stein-Moore 色譜。
敏感性: 易吸潮
介紹:
Brij L23,過(guò)去又稱Brij 35,是乙氧基化(23)天然脂肪醇,基于月桂醇,是月桂醇與環(huán)氧乙烯反應(yīng)生成的醚類的聚氧乙烯化合物,為非離子表面活性劑。這個(gè)天然衍生的表面活性劑提供了多種功能優(yōu)勢(shì),包括潤(rùn)濕劑和高發(fā)泡特性。 Brij L23屬非離子型去污劑,通過(guò)膜滲透有效分離親水性蛋白質(zhì)和疏水性蛋白質(zhì),而不改變其生物學(xué)活性。 化學(xué)基團(tuán):非離子型表面活性劑- 乙氧基化脂肪醇·"
QT-00055 金黃色葡萄球菌ATCC33591 凍干粉
QT-00057 大腸埃希氏菌ATCC35218 凍干粉
QT-00059 屎腸球菌ATCC35667 凍干粉
QT-00061 變異鏈球菌ATCC35668 凍干粉
QT-00063 遲緩真桿菌/遲緩埃格特菌ATCC43055 凍干粉
QT-00065 金黃色葡萄球菌ATCC43300 凍干粉 【聚氧乙烯月桂醚CAS:9002-92-0】
QT-00067 弗氏檸檬酸桿菌ATCC43864 凍干粉
QT-00069 淋病柰瑟氏菌ATCC49226 凍干粉
QT-00071 流感嗜血桿菌ATCC49247 凍干粉
QT-00072 肺炎鏈球菌ATCC49619 凍干粉
QT-00074 流感嗜血桿菌ATCC49766 凍干粉
QT-00076 糞腸球菌(高耐)ATCC51299 凍干粉
QT-00078 阪崎腸桿菌ATCC51329 凍干粉
QT-00080 克柔念珠菌ATCC6258 凍干粉
QT-00082 金黃色葡萄球菌ATCC6538 凍干粉
QT-00084 枯草芽孢桿菌ATCC6633 凍干粉
QT-00086 肺炎克雷伯菌ATCC700603 凍干粉
QT-00088 熱帶念珠菌ATCC750 凍干粉
QT-00090 嗜熱脂肪地芽孢桿菌ATCC7953 凍干粉
QT-00092 植物乳桿菌ATCC8014 凍干粉
QT-00094 大腸埃希氏菌ATCC8739 凍干粉
QT-00096 白色假絲酵母/白色念球菌ATCC90029 凍干粉 【聚氧乙烯月桂醚CAS:9002-92-0】
QT-00100 銅綠假單胞桿菌(綠膿桿菌)ATCC9027 凍干粉
QT-00102 枯草芽孢桿菌黑色變種ATCC9372 凍干粉
QT-00103 艱難梭菌ClostridiumdifficileATCC9689 凍干粉
QT-00104 啤酒酵母ATCC9763 凍干粉
QT-00105 黑曲霉ATCC10582 凍干粉
QT-00106 磚紅鏈霉菌ATCC19776 凍干粉
QT-00107 白色葡萄球菌ATCC8799 凍干粉
QT-00108 皺褶青霉ATCC10128 凍干粉
QT-00109 黑曲霉ATCC10864 凍干粉
QT-00110 釀酒酵母ATCC26603 凍干粉
QT-00111 釀酒酵母ATCC26785 凍干粉
9238888 PCB, Main-01, BS96 CNY
9238886 Cable, HM, BS96 CNY 【聚氧乙烯月桂醚CAS:9002-92-0】
9238854 #BR M96, Basic Agreement The Basic Cover Agreement M96 provides full service coverage for the BioRobot M96. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY
9238842 RS232 box, non-online fill, RapidPlate CNY
9241215 Full Agreement Depot Repair, Shaker, 1yr "The Full Agreement Depot Repair, Shaker provides full service coverage for the plate shaker used in the digene HPV application. The service is conducted as an instrument exchange service.
All shipping, labor and repair part costs related to an instrument exchange are included for 1 year. Instrument exchange time is 2 - 3 working days." CNY
9238833 #BR 9604, Basic Agreement The Basic Cover Agreement 9604, 1 PM provides full service coverage for the BioRobot 9604. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY
9238832 BR 9600, Basic Agreement The Basic Cover Agreement 9600 provides full service coverage for the BioRobot 9600. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY
9238819 Rect. carrier for 5 glass tubes 25ml CNY
9237527 Software LiquiChip Workstation IS V2.2. CNY
9237380 Installation, BR MDx & 2 react. setup Installation and training, including two customized reaction setup protocols CNY
9237379 Installation, BR MDx & 1 react. setup Installation and training, including one customized reaction setup protocol CNY
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
9237175 Guard Fan, Platic XYP CNY
9233209 Tubing, 3/2, CNY
9233155 Power Cord, European CNY
9236418 Board, CPU, TWI CNY
9236345 Red LSR CNY
9236166 Safety shield, RapidPlate CNY 【聚氧乙烯月桂醚CAS:9002-92-0】
9230863 Anpressplatte Rose-80 CNY
9235538 Teaching Tool CNY
9230282 Cable, RS323, robot to syringe pump, 225 CNY
5050-2002 hc2 Software V2 Package CNY
BS96RNA BioSprint 96 to RNA (384) - UDP CNY
9240730 Tubing, 1/4" OD, Red, AP CNY
9240713 Poly Muffler Kit, AP96/196 CNY
9240690 Bearings, Lead Screws, AP CNY
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
6000-5013 LumiCheck Plate User Package CNY
288103 bactotype Mycoplasma Mg/Ms PCR Kit (24) CNY
1048147 QIAamp Viral RNA Mini Accessory Set CNY
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