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伪狂犬病毒抗体检测试剂盒
点击次数：9发布时间：2016/6/19 21:26:30
更新日期：2016/6/19 21:26:30
所 在 地：中国大陆
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相关标签：伪狂犬病毒抗体检测试剂盒
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【伪狂犬病毒抗体检测试剂盒】齐一生物科技（上海）有限公司是一家专业销售生化检测试剂盒.酶联免疫试剂盒,抗体蛋白.生化试剂,标准品和对照品的大型化学科技公司.自公司成立以来,本着始终拥有的创业激情,公司的销售额保持高速增长,企业规模不断扩大. 齐一生物销售：021－6034 8496；181214 53965；173021 04490网址：www.qiyibio.com
QT-00267表皮葡萄球菌CMCC(B)26069冻干粉
QT-00268普通变形杆菌CMCC(B)49027冻干粉
QT-00269福氏志贺氏菌CMCC(B)26003冻干粉
QT-00270痢疾志贺氏菌CMCC(B)51252冻干粉
QT-00271福氏志贺氏菌CMCC(B)51572冻干粉
QT-00272宋氏志贺氏菌CMCC(B)51592冻干粉
QT-00273阴沟肠杆菌CMCC(B)45301冻干粉
QT-00274肠埃希氏菌CMCC(B)44103冻干粉
QT-00275单核增生性李斯特氏菌CMCC(B)54002冻干粉
QT-00276已型副伤寒沙门氏菌CMCC(B)50094冻干粉
QT-00277枯草芽孢杆菌CMCC(B)63501冻干粉
QT-00278小肠结肠炎耶尔森氏菌CMCC(B)52204冻干粉
QT-00279粘质沙雷伯氏菌CMCC(B)41002冻干粉
QT-00280产气肠杆菌CMCC(B)45103冻干粉
QT-00281肺炎克雷伯氏菌CMCC(B)46117冻干粉
QT-00282蜡样芽孢杆菌CMCC(B)63301冻干粉
QT-00283短小芽孢杆菌CMCC(B)63202冻干粉
QT-00284铜绿假单胞菌CMCC(B)10104冻干粉
QT-00285大肠埃希氏菌CMCC(B)44102冻干粉
QT-00286鼠伤寒沙门氏菌CMCC(B)50115冻干粉
QT-00287黑曲霉CMCC(B)98003冻干粉
QT-00288大肠埃氏菌8099冻干粉
QT-00289非01霍乱弧菌Vb0冻干粉
QT-00290伤寒沙门氏菌CMCC(B)50071冻干粉
QT-00291德氏乳杆菌保加利亚亚种CICC6045冻干粉
QT-00292乳链球菌CICC6016冻干粉
QT-00293瑞士乳杆菌CICC6024冻干粉
QT-00294巴氏醋杆菌巴氏亚种CICCT006冻干粉
QT-00295丙酮丁醇梭菌（丙酮丁醇杆菌）CICC8011冻干粉
QT-00296白球拟酵母CICC1040冻干粉
74182RNeasy 96 Kit (12)For 12 x 96 total RNA preps: 12 RNeasy 96 Plates, Elution Microtubes CL (1.2 ml), Caps, RNase-free Reagents ａnd BuffersCNY
74136RNeasy Plus Mini Kit (250)CNY
28004MinElute PCR Purification Kit (50)50 MinElute Spin Columns, Buffers, Collection Tubes (2 ml)CNY
74124RNeasy Protect Mini Kit (50)RNAlater RNA Stabilization Reagent (50 ml), 50 RNeasy Mini Spin Columns, Collection Tubes (1.5 ml ａnd 2 ml), RNase-free Reagents ａnd BuffersCNY
19588Elution Microtubes CL (24 x 96)CNY
19133QIAGEN Proteinase K (10)10 ml (>600 mAU/ml, solution)CNY
19076Buffer ATL200 ml Tissue Lysis Buffer for 1000 prepsCNY
19048EndoFree Plasmid Buffer SetBuffers P1, P2, P3, QBT, QC, QN, ER, TE, Endotoxin-free water, RNase A; for 10 plasmid mega- or 5 gigapreps (endotoxin-free)CNY
12961QIAGEN Plasmid Plus Maxi Sample Kit (5)QIAGEN Plasmid Plus Kits enable ultrafast, large-scale plasmid purification of pure plasmid DNA. The use of a vacuum manifold allows purification of up to 12 (Mega ａnd Giga) or up to 24 (Midi ａnd Maxi) samples in parallel with low hands-on needs. Low elution volumes yield highly concentrated plasmid DNA for direct use without ethanol precipitation. QIAGEN Plasmid Plus Kits also feature a novel wash buffer for endotoxin reduction.CNY
12243QIAfilter Plasmid Midi Kit (25)25 QIAGEN-tip 100, Reagents, Buffers, 25 QIAfilter Midi CartridgesCNY
12123QIAGEN Plasmid Mini Kit (25)25 QIAGEN-tip 20, Reagents, BuffersCNY
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4503065artus CMV LC PCR Kit (96) CECNY
6000-5000Specimen Collection TubesCNY
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5128-1220Specimen Transport Medium (STM) CECNY
5123-1220Female Swab Specimen Collection KitTMCNY
5100-1400IVDhc2 Sample Conversion KitCNY
EA11424EASYartus BKV RG_IICNY
5050-1075 V.1CD Rom Manual, MST Vortexer 2CNY
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9240729Tubing, 3/8"OD , Red, APCNY
9240719Cable Carrier, Capper, Elevator, APCNY
9240701O-Ring, Shaker, Lower Body, AP96/196CNY
9240696Fitting, Barbed, 1/4" ID tube, APCNY
9243651Comprehen Valid., QIAgility"""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
218076miScript SYBR Green PCR Kit (2000)CNY
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