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Anti-Skp2 (S-phase kinase-associated protein 2,SKP2)細胞S相激酶相關
點擊次數(shù):12發(fā)布時間:2016/7/23 16:27:16

更新日期:2016/7/23 16:27:16
所 在 地:中國大陸
產品型號:
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【Anti-Skp2 (S-phase kinase-associated protein 2,SKP2)細胞S相激酶相關蛋白抗體】齊一生科技(上海)有限公司感謝您的查閱與咨詢!期待與您的真誠合作!
低價格現(xiàn)貨供應,歡迎前來選購齊一生物銷售:021-6034 8496;181214 53965;173021 04490網站:www.qiyibio.com【Anti-Skp2 (S-phase kinase-associated protein 2,SKP2)細胞S相激酶相關蛋白抗體】
QYD586 禽腦脊髓炎ELISA試劑盒(AE-Ab) 96孔/盒
QYD587 傳染性喉氣管炎ELISA試劑盒(ILT-Ab) 96孔/盒
QYD588 鴨腸炎沙門氏菌ELISA試劑盒(SE-Ab) 96孔/盒
QYD589 鴨鼠傷寒沙門氏菌ELISA試劑盒 (ST-Ab) 96孔/盒
QYD590 雞傳染性貧血ELISA試劑盒(CAV-Ab) 96孔/盒
QYD591 偽狂犬 -抗體檢測ELISA 96孔/盒
QYD592 豬瘟 - 抗體檢測ELISA 96孔/盒 【Anti-Skp2 (S-phase kinase-associated protein 2,SKP2)細胞S相激酶相關蛋白抗體】
QYD593 豬瘟 - 抗原檢測 ELISA 96孔/盒
QYD594 口蹄疫-NS(3ABC) - 抗體檢測ELISA 96孔/盒
QYD595 口蹄疫-NS(3ABC)- 抗體檢測ELISA 96孔/盒
QYD596 口蹄疫 - 抗體檢測ELISA 96孔/盒
QYD597 藍耳病 - 抗體檢測ELISA 96孔/盒
QYD598 圓環(huán)病毒 IgG - 抗體檢測ELISA 96孔/盒
QYD599 豬水泡病毒 - 抗體檢測ELISA 96孔/盒
QYD600 豬細小病毒 - 抗體檢測ELISA: Ceditest PPV 96孔/盒
QYD601 豬傳染性胸膜肺炎 - 抗體檢測ELISA:Ceditest APP 96孔/盒
QYD602 豬瘟 - 抗體檢測ELISA 96孔/盒
QYD603 豬傳染性胸膜肺炎 - 抗體檢測ELISA 96孔/盒
QYD604 豬丹毒 - 抗體檢測ELISA 96孔/盒
QYD605 豬丹毒 - 抗原檢測ELISA 96孔/盒
QYD606 豬傳染性胃腸炎 - 抗體檢測ELISA 96孔/盒
QYD607 豬沙門氏菌 - 抗體檢測ELISA 96孔/盒
QYD608 豬流感- 抗體檢測ELISA 96孔/盒 【Anti-Skp2 (S-phase kinase-associated protein 2,SKP2)細胞S相激酶相關蛋白抗體】
QYD609 豬流感- 抗原檢測ELISA 96孔/盒
QYD610 豬副嗜血桿菌- 抗體檢測ELISA 96孔/盒
QYD611 豬輪狀病毒- 抗體檢測ELISA 96孔/盒
QYD612 豬輪狀病毒- 抗原檢測ELISA 96孔/盒
QYD613 反芻動物弓形蟲抗體檢測ELISA 96孔/盒
QYD614 非洲豬瘟抗體檢測試劑盒 96孔/盒
QYD615 鯉魚卵黃蛋白原試劑盒 96孔/盒
QYD616 虹鱒魚卵黃蛋白原試劑盒 96孔/盒
QYD617 鮭科魚卵黃蛋白原試劑盒 96孔/盒
74121 RNeasy Protect Starter Kit RNAlater RNA Stabilization Reagent (20 ml), 6 RNeasy Mini Spin Columns, 2 RNeasy Midi Spin Columns, Collection Tubes (1.5 and 2 ml), RNase-free Reagents and Buffers CNY
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 【Anti-Skp2 (S-phase kinase-associated protein 2,SKP2)細胞S相激酶相關蛋白抗體】
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 【Anti-Skp2 (S-phase kinase-associated protein 2,SKP2)細胞S相激酶相關蛋白抗體】
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