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L-丙氨酰胺鹽酸鹽CAS:33208-99-0

點擊次數(shù):13發(fā)布時間:2016/8/24 18:34:26

L-丙氨酰胺鹽酸鹽CAS:33208-99-0

更新日期:2016/8/24 18:34:26

所 在 地:中國大陸

產(chǎn)品型號:

簡單介紹:L-丙氨酰胺鹽酸鹽CAS:33208-99-0 英文名稱:L-Alaninamide hydrochloride 規(guī)格:BR,99% 包裝:5克 齊一生物科技(上海)有限公司銷售:021-6034 8496;181214 53965;173021 04490

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 L-丙氨酰胺鹽酸鹽CAS:33208990齊一生物銷售:0216034 8496181214 53965;173021 04490

齊一生物科技(上海)有限公司是一家專業(yè)銷售生化檢測試劑盒.酶聯(lián)免疫試劑盒,抗體蛋白.生化試劑,標準品和對照品的大型化學科技公司.自公司成立以來,本著始終擁有的創(chuàng)業(yè)激情,公司的銷售額保持高速增長,企業(yè)規(guī)模不斷擴大. L-丙氨酰胺鹽酸鹽CAS:33208990齊一生物科技(上海)有限公司全國熱線:400-991-0197網(wǎng)址:www.qiyibio.com

"L-丙氨酰胺鹽酸鹽CAS:33208990   英文名稱:LAlaninamide hydrochloride   規(guī)格:BR99%   包裝:5      熔點: 212217°C

比旋光度: 11 ° (C=1, MeOH)

儲存條件: RT

介紹: mp : 217 °C [α]20D : 11 ° (C=1, MeOH)"

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QY-L0858       土荊皮甲酸 82508-32-5      Pseudolaric acid A  82508-32-5     20mg                   

QY-L0859       土荊皮乙酸82508-31-4       Pseudolaric Acid B  82508-31-4     20mg                    L-丙氨酰胺鹽酸鹽CAS:33208990

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QY-L0876       五味子乙素61281-37-6       Schisandrin B  61281-37-6     20mg                   

QY-L0877       五味子醇甲7432-28-2  Schisandrin     7432-28-2      20mg                   

QY-L0878       五味子酯甲58546-56-8       Schisantherin A      58546-56-8     20mg                   

QY-L0879       五味子醇乙58546-54-6       Schisandrol B  58546-54-6    20mg                   

QY-L0880       五味子丙素61301-33-5       Schisandrin C 61301-33-5     20mg                   

QY-L0881       戈米辛G       Gomisin G           20mg                   

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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.

 

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