產(chǎn)品展示
IL-8白介素8(白細(xì)胞介素-8)(抗原)
點(diǎn)擊次數(shù):18發(fā)布時(shí)間:2016/7/23 18:19:12

更新日期:2016/7/23 18:19:12
所 在 地:中國(guó)大陸
產(chǎn)品型號(hào):
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詳細(xì)內(nèi)容
【IL-8白介素8(白細(xì)胞介素-8)(抗原)】齊一生物專(zhuān)業(yè)經(jīng)營(yíng)銷(xiāo)售通用試劑.分析試劑.標(biāo)準(zhǔn)物質(zhì).合成試劑.中間體.催化劑.生化試劑等化學(xué)產(chǎn)品,我們致力于以專(zhuān)業(yè)化的視角,提供豐富專(zhuān)業(yè)產(chǎn)品資料及其相關(guān)技術(shù)開(kāi)發(fā)資訊,產(chǎn)品內(nèi)容覆蓋分析化學(xué).無(wú)機(jī)化學(xué).有機(jī)化學(xué).生命科學(xué).材料科學(xué)等領(lǐng)域. 【IL-8白介素8(白細(xì)胞介素-8)(抗原)】已迅速發(fā)展成為國(guó)內(nèi)科學(xué)試劑的運(yùn)營(yíng)商,是國(guó)家重點(diǎn)實(shí)驗(yàn)室指定供應(yīng)商,并與國(guó)內(nèi)多家科研單位緊密合作. 齊一生物銷(xiāo)售:021-6034 8496;181214 53965;173021 04490網(wǎng)站:http://www.qiyibio.com
【IL-8白介素8(白細(xì)胞介素-8)(抗原)】齊一生物科技(上海)有限公司經(jīng)營(yíng)試劑種類(lèi)眾多:覆蓋分析化學(xué)品,無(wú)機(jī)化學(xué)品,有機(jī)化學(xué)品,生物化學(xué)品,材料化學(xué)品等.試劑信息齊全:包含試劑特性描述,詳細(xì)質(zhì)量信息,應(yīng)用方法.標(biāo)準(zhǔn), 科研 用途以及正在開(kāi)發(fā)的前沿應(yīng)用歡迎前來(lái)選購(gòu)。齊一生物銷(xiāo)售:021-6034 8496;181214 53965;173021 04490網(wǎng)站:http://www.qiyibio.com
9238815 Rect. carrier for 12 tubes 10 ml w/ cap CNY
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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
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9019143 Power supply, PyroQ96 CNY
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9015690 Rings (10), pinching, 4.5/3.2 mm CNY
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QY-x1188 人乳腺癌細(xì)胞MB-271
QY-x1189 人乳腺癌細(xì)胞ER-30
QY-x1190 人乳腺癌細(xì)胞M453
QY-x1191 人乳腺浸潤(rùn)性導(dǎo)管癌旁皮膚細(xì)胞CCD-1095Sk
QY-x1192 人乳腺細(xì)胞HBL-100
QY-x1193 人乳腺導(dǎo)管瘤細(xì)胞UACC812
QY-x1194 人乳腺癌細(xì)胞系1590 【IL-8白介素8(白細(xì)胞介素-8)(抗原)】
QY-x1195 人卵巢癌細(xì)胞A2780
QY-x1196 人卵巢癌細(xì)胞Sw626
QY-x1197 人卵巢癌順鉑耐藥株COC1/CDDP
QY-x1198 人卵巢癌紫杉醇耐藥株A2780/Taxol
QY-x1199 人卵巢癌細(xì)胞系Anglne
QY-x1200 人卵巢癌細(xì)胞OVCaR-3
QY-x1201 人卵巢癌細(xì)胞Caov-3
QY-x1202 人卵巢癌細(xì)胞HO-8910
QY-x1203 人高轉(zhuǎn)移卵巢癌細(xì)胞HO-8910PM
QY-x1204 人卵巢癌細(xì)胞8910PM
QY-x1205 人卵巢癌細(xì)胞HOC1
QY-x1206 人卵巢癌細(xì)胞COC1
QY-x1207 人卵巢癌細(xì)胞OVAC
QY-x1208 人卵巢癌細(xì)胞Ovary
QY-x1209 人卵巢畸胎瘤細(xì)胞PA-1
QY-x1210 人卵巢癌細(xì)胞SK-OV-3 【IL-8白介素8(白細(xì)胞介素-8)(抗原)】
QY-x1211 人卵巢透明細(xì)胞癌細(xì)胞ES-2
QY-x1212 人卵巢癌細(xì)胞系3AO
QY-x1213 人子宮內(nèi)膜癌細(xì)胞ISK (Ishikawa)
QY-x1214 人子宮內(nèi)膜腺癌細(xì)胞HEC-1-A
QY-x1215 人子宮內(nèi)膜腺癌細(xì)胞HEC-1-B
QY-x1216 人子宮內(nèi)膜腺癌細(xì)胞AN3 CA
QY-x1217 人子宮內(nèi)膜腺癌細(xì)胞KLE
QY-x1218 人宮頸癌細(xì)胞HeLa
QY-x1219 人Hela細(xì)胞耐藥亞株(Hela/DDP)Hela