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L-苯丙氨酸甲酯鹽酸鹽CAS:7524-50-7
點擊次數(shù):14發(fā)布時間:2016/8/30 16:08:52

更新日期:2018/3/30 11:59:03
所 在 地:中國大陸
產(chǎn)品型號:
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"L-苯丙氨酸甲酯鹽酸鹽CAS:7524-50-7 英文名稱:H-Phe-OMe•HCl 規(guī)格:特純,98.0% 包裝:10克 熔點: 158-162 °C
比重: 1·092
比旋光度: 38 ° (C=2, EtOH)
儲存條件: RT
用途: 用于生化試劑,醫(yī)藥中間體。
敏感性: 易吸潮"
QT-00470 皺褶青霉 支 上海 820
QT-00471 串珠鐮刀菌 支 上海 820
QT-00472 嗜熱脂肪地芽孢桿菌 支 上海 820
QT-00476 單增李斯特氏菌 ATCC 19111 支 上海 820
QT-00477 單核細胞增生李斯特氏菌 支 上海 460
QT-00478 福氏志賀氏菌(Shigella flexneri) 支 上海 460
QT-00479 兩歧雙歧桿菌 ATCC 29521 支 上海 1500 【L-苯丙氨酸甲酯鹽酸鹽CAS:7524-50-7】
QT-00480 嬰兒雙歧桿菌 ATCC 15697 支 上海 1500
QT-00481 長雙歧桿菌 支 上海 460
QT-00482 青春雙歧桿菌 ATCC 15703 支 上海 1500
QT-00483 動物雙歧桿菌 支 上海 1500
QT-00484 短雙歧桿菌 ATCC 15700 支 上海 1500
QT-00485 干酪乳桿菌干酪亞種 支 上海 460
QT-00486 德氏乳桿菌保加利亞亞種 支 上海 460
QT-00487 嗜酸乳桿菌 支 上海 460
QT-00488 羅伊氏乳桿菌 支 上海 820
QT-00489 鼠李糖乳桿菌 支 上海 820
QT-00490 植物乳桿菌 支 上海 460
QT-00491 嗜熱乳酸鏈球菌 支 上海 460
QT-00492 出血性大腸埃希氏菌 支 上海 820
QT-00493 阪崎腸桿菌 支 上海 460
QT-00494 德氏乳桿菌乳酸亞種 支 上海 460
QT-00495 鼠李糖乳桿菌 ATCC 7469 2支 美國 MBL 1810 【L-苯丙氨酸甲酯鹽酸鹽CAS:7524-50-7】
QT-00496 大腸埃希氏菌 ATCC 25922 支 上海 400
QT-00497 大腸埃希氏菌 ATCC 25922 2支 美國 MBL 1400
QT-00498 大腸埃希氏菌 ATCC 25922 5支 美國 MBL 2600
QT-00499 糞腸球菌 ATCC 29212 支 上海 400
QT-00500 糞腸球菌 ATCC 29212 2支 美國 MBL 1550
QT-00501 糞腸球菌 ATCC 29212 5支 美國 MBL 2620
QT-00502 產(chǎn)氣莢膜梭菌 ATCC 13124 支 上海 460
QT-00503 產(chǎn)氣莢膜梭菌 ATCC 13124 2支 美國 MBL 1810
9240520 Motor Assy, Sz. 17, Common, AP98 CNY
9240102 Re-Installation, LiquiChip The Re-Installation, LiquiChip facilitates quick implementation of system back into lab routine by minimizing instrument set-up phase. It covers hardware and software check of instrument and provides user with operator refesher overview. Re-installation includes labor and travel costs. Re-installation performance process is documented on a GMP/GLP-compliant Field Service document. CNY
9019940 Power supply, vac pump, CX1 CNY
9019477 LASER MODUAL GS CNY
9019476 Spacer, 0.2 mm short set, GSC CNY
9238888 PCB, Main-01, BS96 CNY
9238886 Cable, HM, BS96 CNY 【L-苯丙氨酸甲酯鹽酸鹽CAS:7524-50-7】
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 【L-苯丙氨酸甲酯鹽酸鹽CAS:7524-50-7】
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