產(chǎn)品展示
ER-α(Estrogen)雌激素受體(抗原)
點擊次數(shù):21發(fā)布時間:2016/7/22 16:06:08

更新日期:2016/7/22 16:06:08
所 在 地:中國大陸
產(chǎn)品型號:
優(yōu)質(zhì)供應(yīng)
詳細內(nèi)容
【ER-α(Estrogen)雌激素受體(抗原)】齊一生物長期經(jīng)營生化檢測試劑盒及抗體(免費代測)、分子學生物試劑盒、比色法,IFCC推薦法,化學氧化法,速率法、高效液相色譜法、可見分光光度法、紫外分光光度法、酶標法檢測試劑盒等檢測試劑盒、誠信經(jīng)營,價格實惠,服務(wù)周到,質(zhì)量保障!提供各種實驗代測服務(wù)。【ER-α(Estrogen)雌激素受體(抗原)】齊一生物銷售:021-6034 8496;181214 53965;173021 04490網(wǎng)址:www.qiyibio.com
QY-x1124 Ad5DNA轉(zhuǎn)化的胚腎HEK-293
QY-x1125 人原胚腎轉(zhuǎn)化細胞系293 Ad5+
QY-x1126 表達SV40T抗原人胚腎上皮細胞293FT
QY-x1127 人人胚腎細胞AAV-293
QY-x1128 人胚腎上皮包裝細胞GP2-293
QY-x1129 人胚腎上皮包裝細胞GP2-293Luc
QY-x1130 人腎上腺腺瘤細胞NCI-H205 【ER-α(Estrogen)雌激素受體(抗原)】
QY-x1131 人胚腎上皮細胞HK-2C
QY-x1132 人腎癌細胞KC
QY-x1133 人胚腎上皮細胞HKC
QY-x1134 人腎小管近段上皮細胞HK-2
QY-x1135 人腎上腺神經(jīng)母細胞瘤細胞(腦轉(zhuǎn)移)KP-N-NS
QY-x1136 人胚腎細胞2V6.11
QY-x1137 人胚腎二倍體細胞CCC-HEK-1
QY-x1138 人腎癌細胞系(769-P)769-P
QY-x1139 人腎透明細胞癌皮膚轉(zhuǎn)移細胞Caki-1
QY-x1140 人腎上腺皮質(zhì)腺癌細胞SW-13
QY-x1141 人腎癌細胞系A498
QY-x1142 人腎癌細胞系ACHN
QY-x1143 人腎癌細胞GRC-1
QY-x1144 人腎上皮細胞GES
QY-x1145 人腎癌Wilms細胞G401
QY-x1146 Asp2人胚胎腎細胞轉(zhuǎn)化細胞FC33 【ER-α(Estrogen)雌激素受體(抗原)】
QY-x1147 人腎癌細胞SK-RC-42
QY-x1148 人膀胱癌細胞EJ
QY-x1149 人膀胱癌細胞5637(HTB-9)
QY-x1150 人膀胱移行細胞癌細胞T24
QY-x1151 人膀胱鱗癌細胞ScaBER
QY-x1152 人膀胱癌細胞BIU-87
QY-x1153 人膽管癌細胞RBE
QY-x1154 人膽管癌細胞QBC939
QY-x1155 人乳腺癌細胞MCF-7
9240630 Power Supply, 5VDC 1.5 AMP, AP96 CNY
9240593 Unload Valve, Pump, Pressure, AP196/98 CNY
9240562 Fuse, PCB, 315, Eppendorf, AP196/98 CNY
9240536 Motor Assy, SiNug, 17, All, AP96/196 CNY
9240514 CD R/W, AP196/98 CNY
9240504 PC-104, AP98 CNY
9240346 Autopure, Full Agreement "Repair service delivery: onsite
Service response time (repair): 48 hours/2 business days
Periodic inspection/maintenance: yes, 1/agreement year
Inspection/maintenance delivery: onsite
Cost coverage for repair parts: yes, included
Cost coverage for labor: yes, included
Cost coverage for travel: yes, included
Replacement system (Loaner) provision: not included
Transportation cost coverage: not applicable" CNY
9240098 Re-Installation, BR EZ1 The Re-Installation, BR EZ1 facilitates quick implementation of system back into lab routine by minimizing instrument set-up phase. It covers hardware and software check of instrument and provides user with operator refesher overview. Re-installation includes labor and travel costs. Re-installation performance process is documented on a GMP/GLP-compliant Field Service document. CNY
9239852 Foot bumpers, v2.0 (4) CNY
9019944 Cable, P-axis, wires, 8 ch. , C18 CNY
9238880 Bearings up. & low, BS96 CNY
9238836 BioSprint96, Basic Agreement, no PM "Repair service delivery: onsite
Service response time (repair): 5 business days
Periodic inspection/maintenance: not included
Inspection/maintenance delivery: not applicable
Cost coverage for Repair Parts : yes, full coverage
Cost coverage for labor: yes, full coverage
Cost coverage for travel: yes, full coverage
Replacement system (Loaner) provision: not applicable
Transportation cost coverage: not applicable" CNY
9241211 Full Agreement Depot Repair, DML2000, 1y "The Full Agreement Depot Repair, DML2000 provides full service coverage for the DML 2000 luminometer. The service is conducted as an instrument exchange service.
All shipping, labor and repair part costs related to an instrument exchange are included for 1 year. Instrument exchange time is 2 - 3 working days." CNY
9241191 Magnet, tool, QX CNY 【ER-α(Estrogen)雌激素受體(抗原)】
9238825 Spare bucket for plate rotor CNY
9238815 Rect. carrier for 12 tubes 10 ml w/ cap CNY
9019472 TAPE SPACER CLEAR GS CNY
9019464 UV tube, Cxx CNY
9243650 Comprehen Valid., EZ1/QIAcube/QIAsymph """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
9237333 Install, BR plus 3 integr. w. scheduling Installation and training, BioRobot System including three approved integration devices with scheduling CNY
9237328 Upgrade, BR & 2 ext. devices w. sched. Upgrade BioRobot with two approved integration devices using scheduling software CNY
9237173 Shield, V-housing CNY
9233208 Tubing, liquid system 2.5/1.5 CNY
9237155 V-Housing with Sample Needle CNY
9237150 Heater Top CNY
9016151 #App. Package, M48, Pathology CNY
9019179 Opto - plate lock closed, PyroQ96MD CNY
9011883 Upgrade, high speed pipetting system CNY
9011882 Back unit, BR9600 CNY
9011823 Z-Modul; Tip-Adapter 300µl; BR8000 CNY 【ER-α(Estrogen)雌激素受體(抗原)】
9236916 3 Year Warranty, LiquiChip LiquiChip 3-year Warranty with 1 Preventive Maintenance per year. Included in system price. This warranty must be included as a line item on the system quote. It covers the system for three years total including all per incident travel and labor charges, all repair parts, one preventive maintenance visits per year (three in total), and 48- hour priority response. CNY