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CD73 (5′-nucleotidase cytosolicⅡ)胞漿-5′-核苷酸酶-Ⅱ 抗原
點(diǎn)擊次數(shù):20發(fā)布時(shí)間:2016/7/23 13:07:52

更新日期:2016/7/23 13:07:52
所 在 地:中國(guó)大陸
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【CD73 (5´-nucleotidase cytosolicⅡ)胞漿-5´-核苷酸酶-Ⅱ 抗原】齊一生科技(上海)有限公司感謝您的查閱與咨詢!期待與您的真誠(chéng)合作!
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DQYC70 茶飲料中茶多酚的快速檢測(cè)試劑盒 50次/袋
DQYC71 飲料苯甲酸檢測(cè)試劑盒 50次/袋
DQYC72 氟乙酰胺速測(cè)盒 40次/袋
DQYC73 砷、銻、鉍、汞、銀化物檢測(cè)試劑 30次/袋
DQYC74 檢砷管速測(cè)盒 30次/袋
DQYC75 檢汞管速測(cè)盒 30次/袋
DQYC76 肉制品色素速測(cè)盒 50次/袋 【CD73 (5´-nucleotidase cytosolicⅡ)胞漿-5´-核苷酸酶-Ⅱ 抗原】
DQYC77 豆?jié){生熟度的檢測(cè) 80次/袋
DQYC78 雞蛋新鮮度速測(cè)劑 200ml/袋
DQYC79 食用油中桐油速測(cè)鑒別試劑 50次/袋
DQYC80 食用油中大嘛油速測(cè)鑒別試劑 10次/袋
DQYC81 食用油中巴豆油速測(cè)鑒別試劑 10次/袋
DQYC82 食用油中礦物油速測(cè)鑒別試劑 10次/袋
DQYC83 蜂蜜酸度速測(cè)液 25次/袋
DQYC84 蜂蜜中飴糖速測(cè)液 100次/袋
DQYC85 蜂蜜比重計(jì)(水分測(cè)定) 比重計(jì)
DQYC86 蜂蜜中蔗糖含量速測(cè)液(定性) 100次/袋
DQYC87 蜂蜜中蔗糖含量速測(cè)液(半定量)
DQYC88 蜂蜜中果糖、葡萄糖速測(cè)液 100次/袋
DQYC89 液態(tài)奶中摻加甲醛的檢測(cè)試劑 100次/袋
DQYC90 液態(tài)奶中摻加豆?jié){的檢測(cè)試劑 100次/袋
DQYC91 液態(tài)奶中摻加淀粉的檢測(cè)試劑 60次/袋
DQYC92 液態(tài)奶中摻加硼酸鹽的檢測(cè)試劑 100次/袋 【CD73 (5´-nucleotidase cytosolicⅡ)胞漿-5´-核苷酸酶-Ⅱ 抗原】
DQYC93 液態(tài)奶中摻加尿素的檢測(cè)試劑 50次/袋
DQYC94 液態(tài)奶中摻加食鹽的檢測(cè)試劑 50次/袋
DQYC95 液態(tài)奶中摻加碳酸鈉的檢測(cè)試劑 50次/袋
DQYC96 液態(tài)奶中摻加亞硝酸鹽的檢測(cè)試劑 100次/袋
DQYC97 液態(tài)奶中摻加銨鹽的檢測(cè)試劑 50次/袋
DQYC98 乳稠計(jì)(奶純度) 乳稠計(jì)
DQYC99 碘鹽含量速測(cè)液 200次/袋
DQYC100 游離性余氯速測(cè)盒 200次/袋
DQYC101 水解蛋白快速檢測(cè)試劑盒 50次/袋
74104 RNeasy Mini Kit (50) 50 RNeasy Mini Spin Columns, Collection Tubes (1.5 ml and 2 ml), RNase-free Reagents and Buffers CNY
72251 TurboCapture 96 mRNA Kit (5) For rapid and easy mRNA purification in high-throughput applications. The kit provides a fast and simple procedure for purifying mRNA. Up to 96 samples can be processed simultaneously - ideal for high-throughput applications such as compound screening and target validation (e.g. by siRNA screening). CNY
19407 VacConnectors (500) 500 disposable connectors for use with QIAamp spin columns on luer connectors. Should be ordered in conjuntion with 19408 - VacValves (24). CNY
12281 QIAfilter Plasmid Mega Kit (5) 5 QIAGEN-tip 2500, Reagents, Buffers, 5 QIAfilter Mega-Giga Cartridges CNY
12191 QIAGEN Plasmid Giga Kit (5) 5 QIAGEN-tip 10000, Reagents, Buffers CNY
4502103 artus VZV TM PCR Kit (24) RUO CNY
133271 NeXtalStock PIPES pH 7.0 (200) CNY
133270 NeXtalStock Phosphate-citr. pH 5.2 (200) CNY 【CD73 (5´-nucleotidase cytosolicⅡ)胞漿-5´-核苷酸酶-Ⅱ 抗原】
990512 Filter-Tips, 50 µl (960) CNY
337620 qBiomarker SYBR Green Fluor Mastermix(2) CNY
337011 qBiomarker Somatic Mutations PCR Assays CNY
4500263 artus HSV-1/2 RG PCR Kit (24) CE CNY
939016 Buffer ATL ( 4 x 50 ml),GPR CNY
4500163 artus HSV-1/2 TM PCR Kit (24) CE CNY
1073925 Ni-NTA Superflow (8 x 500 ml),cus,G CNY
9010931 BGR Greifer P7 (alt) CNY
9010858 BGR DT-Abstreifer 8-fach P7xxx D CNY
931036 QIAsymphony Virus/Bact Mini Kit (192) CNY
133248 NeXtalStock Sodium succinate pH6.5 (200) CNY
330603 RT² SYBR Green FAST Mastermix (24) CNY
929608 QX Pro Separation Buffer (40 ml) CNY
5000-1415 Knob RB671CSKWL Matte, VTX2 CNY
5000-1408 Cable Shielded 1/17HP, VTX2 CNY
L2170 hc2 CT/GC HC2 DNA Test PI (CD-ROM) CNY 【CD73 (5´-nucleotidase cytosolicⅡ)胞漿-5´-核苷酸酶-Ⅱ 抗原】
L1971 Rotary Shaker User's Manual CNY
9240705 O-ring Kit, Capper, Spindle, AP CNY
9240693 Actril Sterilant & Test Strips, AP CNY
9243653 Comprehen Valid., Other Extraction 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). 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.
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
386516 Investigator STR GO! Lysis Buffer (200) CNY
208256 QuantiNova Probe PCR Kit (2500) CNY
208254 QuantiNova Probe PCR Kit (500) CNY