产品展示
2,4-二羟基-4’-硝基偶氮苯CAS:74-39-5
点击次数:14发布时间:2016/8/29 21:59:40
更新日期:2018/3/30 11:59:05
所 在 地:中国大陆
产品型号:
优质供应
详细内容
齐一生科技(上海)有限公司感谢您的查阅与咨询!期待与您的真诚合作!
低价格现货供应,欢迎前来选购【2,4-二羟基-4’-硝基偶氮苯CAS:74-39-5】齐一生物科技(上海)有限公司客服热:400 9910 197/021-6034 8496网站:www.qiyibio.com
"2,4-二羟基-4’-硝基偶氮苯CAS:74-39-5 英文名称:Azoviolet 规格:AR 包装:25克 熔点: 199-200°C
比重: 1·45
储存条件: RT,避光
用途: 镁的测定,吸附指示剂。
敏感性: 对湿度敏感
介绍: 能溶于稀碱溶液,呈红紫色,微溶于沸醇、丙酮、乙酸和甲苯,均呈黄色,不溶于水。吸收波长432nm。有刺激性。"
QTR-981 马传染性动脉炎iELISA抗体检测试剂盒
QTR-982 马疱疹病毒抗体检测试剂盒
QTR-983 西尼罗河热IgM抗体检测试剂盒
QTR-984 兔粘液瘤病毒抗体检测试剂盒
QTR-985 兔出血病病毒抗体检测试剂盒
QTR-986 兔出血病病毒抗原检测试剂盒 【2,4-二羟基-4’-硝基偶氮苯CAS:74-39-5】
QTR-987 伯氏疏螺旋体抗体检测试纸条
QTR-988 犬冠状病毒抗体检测试剂盒
QTR-989 犬瘟热IgG检测试剂盒
QTR-990 犬瘟热IgM检测试剂盒
QTR-991 犬细小IgM检测试剂盒
QTR-992 犬细小抗体检测试剂盒
QTR-993 犬细小抗原检测试剂盒
QTR-994 犬细小抗原检测试纸条
QTR-995 犬艾利希体抗体检测试剂盒
QTR-996 犬艾利希体抗体检测试纸条
QTR-997 犬心丝虫抗原检测试纸条
QTR-998 犬利什曼抗体检测试剂盒
QTR-999 犬利什曼抗体检测试纸条
QTR-1000 狂犬病抗原检测试剂盒
QTR-1001 FELINE specialties猫病
QTR-1002 猫冠状病毒抗体检测试剂盒 【2,4-二羟基-4’-硝基偶氮苯CAS:74-39-5】
QTR-1003 猫白血病抗体检测试剂盒
QTR-1004 猫白血病病毒抗原检测试纸条
QTR-1005 猫白血病抗原p27定量检测试剂盒
QTR-1006 "猫免疫缺陷病(Feline
Immunodefciency (FIV))
"
QTR-1007 猫免疫缺陷病抗体检测试剂盒
QTR-1008 猫免疫缺陷病抗体检测试纸条
QTR-1009 猫免疫缺陷病抗体定量检测试剂盒
QTR-1010 布鲁氏菌PCR测试剂盒 24次
QTR-1011 副结核分枝杆菌PCR检测试剂盒 100次
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 【2,4-二羟基-4’-硝基偶氮苯CAS:74-39-5】
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
180984 GeneRead Adapter I Set 12plex (72) CNY
614035 careHPV Test, SFDA (96-test) CNY
282605 virotype Influenza A RT-PCR Kit (96) CNY
272703 pigtype PRRSV Ab (5) CNY
273003 pigtype Salmonella Ab (5) CNY
280377 virotype BVDV RT-PCR Kit (480) CNY
9018462 Marker Kit, QC tool, QX CNY
800372 Shipping, Postage, Packaging (express) CNY
800373 Data Carrier CNY 【2,4-二羟基-4’-硝基偶氮苯CAS:74-39-5】
9019521 ZLV ADAPTER KIT M&N 8 STRIP CNY
9019595 ZLV Bush, tip stripper, Cx8 CNY
9019935 Cable harness, X-axis 8 core, CQX CNY
9020596 Tape Foam,045X750 Double Stick,DML 3000 CNY
9017843 Tool, cable, communication, RS232, QIAC CNY
9013401 Cable set, cooling system, 90/120 CNY
9234873 ZLVPipetting Station for 2 microtit. CNY
9013395 Tip disposal bags CNY
9013391 Tubing set, PVC, BR9604 CNY