產(chǎn)品展示
Anti-GR (Glucocorticoid receptor)糖皮質(zhì)激素受體抗體
點(diǎn)擊次數(shù):9發(fā)布時(shí)間:2016/7/20 16:38:10

更新日期:2016/7/20 16:38:10
所 在 地:中國(guó)大陸
產(chǎn)品型號(hào):
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詳細(xì)內(nèi)容
【Anti-GR (Glucocorticoid receptor)糖皮質(zhì)激素受體抗體】齊一生物科技(上海)有限公司檢測(cè)試劑盒產(chǎn)品已被廣泛應(yīng)用于化學(xué)、化工、生命科學(xué)的基礎(chǔ)研究和開(kāi)發(fā)應(yīng)用、制藥、疾病診斷與控制、人口與健康、生物技術(shù)等諸多領(lǐng)域?蛻舯椴紘(guó)內(nèi)各大學(xué)、研究所、醫(yī)院、衛(wèi)生防疫、商品檢驗(yàn)檢疫、制藥公司、生物技術(shù)公司和食品工業(yè)等單位。【Anti-GR (Glucocorticoid receptor)糖皮質(zhì)激素受體抗體】齊一生物銷(xiāo)售:021-6034 8496;181214 53965;173021 04490網(wǎng)址:www.qiyibio.com
QY-x1252 人前列腺上皮細(xì)胞RWPE2
QY-x1253 人男性正常龜頭細(xì)胞系HS68
QY-x1254 小兒包皮細(xì)胞HFF
QY-x1255 人正常前列腺上皮細(xì)胞RWPE-1
QY-x1256 人慢性髓原白血病細(xì)胞K562
QY-x1257 人白血病阿霉素耐藥株K562/Adr
QY-x1258 人原髓細(xì)胞白血病細(xì)胞HL60
QY-x1259 人白血病阿霉素耐藥株HL-60/Ad Anti-GR (Glucocorticoid receptor)糖皮質(zhì)激素受體抗體
QY-x1260 人紅白細(xì)胞白血病細(xì)胞ErythroleukemiaHEL
QY-x1261 人白血病細(xì)胞SK
QY-x1262 人急性早幼粒白血病細(xì)胞(懸浮)NB4
QY-x1263 人白血病細(xì)胞Daudi
QY-x1264 人白血病細(xì)胞KG-1
QY-x1265 人T細(xì)胞白血病細(xì)胞6T-CEM
QY-x1266 人T細(xì)胞白血病細(xì)胞HuT 78
QY-x1267 人T細(xì)胞白血病細(xì)胞A3
QY-x1268 人單核細(xì)胞白血病細(xì)胞THP-1
QY-x1269 人肥大細(xì)胞白血病細(xì)胞CHMAS
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QY-x1273 急性T細(xì)胞白血病細(xì)胞)Jurkat
QY-x1274 人T淋巴瘤轉(zhuǎn)基因細(xì)胞Jurkat D,E Anti-GR (Glucocorticoid receptor)糖皮質(zhì)激素受體抗體
QY-x1275 人T淋巴瘤細(xì)胞Jurkat亞系Jurkat77
QY-x1276 人外周血嗜堿性白細(xì)胞KU812
QY-x1277 人原髓細(xì)胞白血病細(xì)胞AL7P/HL-60R
QY-x1278 人急性成髓細(xì)胞白血病Kasumi-1
QY-x1279 人T細(xì)胞白血病細(xì)胞T-CEM
QY-x1280 人EB病毒轉(zhuǎn)化的B細(xì)胞CGM1
QY-x1281 人血液白血病細(xì)胞TF-1
QY-x1282 人分泌A2抗體B淋巴細(xì)胞BB7.2
QY-x1283 人血管平滑肌 T/G
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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
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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
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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
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