產(chǎn)品展示
人合胞病毒(RSV)IGMELISA試劑盒廠家
點(diǎn)擊次數(shù):12發(fā)布時(shí)間:2016/8/17 17:23:54

更新日期:2016/8/17 17:23:54
所 在 地:中國大陸
產(chǎn)品型號:
優(yōu)質(zhì)供應(yīng)
詳細(xì)內(nèi)容
1.購買我公司任意ELISA試劑盒指標(biāo)享受免費(fèi)代測,并提供技術(shù)指導(dǎo)服務(wù)!
二、實(shí)驗(yàn)材料與試劑配制:
1. 儀器與材料:酶標(biāo)儀(使用前預(yù)熱30分鐘),微量加液器、吸頭、蒸餾水或去離子水,濾紙。
2. 緩沖液使用:加5ul 的緩沖液于50ul 的樣品中,如果樣品量不夠或者不確定,緩沖液和樣品的混合比例不要小于1:10即可混勻,靜置1小時(shí)備用(如果標(biāo)本是血清或者血漿,此步驟忽略)。
3. 洗液的配制:按1:100的比例配制洗液備用。
齊一生物銷售:021-6034 8496;181214 53965;173021 04490
【人合胞病毒(RSV)IGMELISA試劑盒廠家】三. 仔細(xì)閱讀說明書
1.檢查試劑盒標(biāo)簽上的有效期。如果超過有效期,請勿使用。
2. 按說明書確定所有試劑齊全(數(shù)量、體積)
3. 標(biāo)本制備要規(guī)范,每份標(biāo)本體積要按2-3個復(fù)孔以上的量制備(貯存),盡量分裝做備份。
4.短期內(nèi)無法實(shí)驗(yàn)者,注意低溫保存
5.準(zhǔn)備好所有實(shí)驗(yàn)額外所需物品,(比如移液器,試管,清洗器,酶標(biāo)儀)
6. 按說明書將所用試劑平衡至室溫,根據(jù)檢測標(biāo)本數(shù)量確定所需試劑的量
7.檢查試劑盒內(nèi)每種試劑的貯存條件,保證所有試劑均按照試劑盒內(nèi)說明書推薦的條件存儲。 【人合胞病毒(RSV)IGMELISA試劑盒廠家】
8.檢查不穩(wěn)定或者變質(zhì)的試劑溶液(比如沉淀或變色)。有些試劑,比如標(biāo)準(zhǔn)品稀釋液或者檢測稀釋液,可能在設(shè)計(jì)時(shí)就含有沉淀物。所有試劑在滴入酶標(biāo)板之前,必需充分混勻。而由于沉淀物的特性,在加入酶標(biāo)板之前,必需不停攪拌。
9.保證充分的孵育時(shí)間和溫度。
10.切勿使用不同生產(chǎn)批號的試劑取代現(xiàn)有試劑或混合現(xiàn)有試劑。
11.在混合或溶解蛋白溶液時(shí),避免泡沫產(chǎn)生。
12.在實(shí)驗(yàn)開始之前,安排好實(shí)驗(yàn)流程。在實(shí)驗(yàn)開始之前,清潔工作臺。
13.若有問題,應(yīng)與我公司或代理商的技術(shù)支持聯(lián)系
【人合胞病毒(RSV)IGMELISA試劑盒廠家】四、客戶須知
齊一生物銷售:021-6034 8496;181214 53965;173021 04490
1.在收集標(biāo)本前都必須有一個完整的計(jì)劃,必須清楚要檢測的成份是否足夠穩(wěn)定。我們提倡新鮮標(biāo)本盡早檢測,對收集后當(dāng)天就進(jìn)行檢測的標(biāo)本,及時(shí)儲存在4℃?zhèn)溆,如有特殊原因需要周期收集?biāo)本,請?jiān)炷H〔暮,將?biāo)本及時(shí)分裝后放在-20℃或-70℃條件下保存。因冰室與室溫存在一定溫差,蛋白極易降解,直接影響實(shí)驗(yàn)質(zhì)量,所以避免反復(fù)凍融。部分標(biāo)本也可加入適當(dāng)防腐劑,激素類標(biāo)本需添加抑肽酶。
2.試劑盒代測標(biāo)本的客戶取材前須向我司銷售人員索要說明書,具體操作注意事項(xiàng)請與我司技術(shù)人員溝通。
3.液體類標(biāo)本:標(biāo)本必須為液體,不含沉淀。包括血清、血漿、尿液、胸腹水、腦脊液、細(xì)胞培養(yǎng)上清、組織勻漿等。
4.購買前請?zhí)崆案嬖V我們:您樣本的種屬、樣本數(shù)量、待測指標(biāo)及其它特殊要求。
【人合胞病毒(RSV)IGMELISA試劑盒廠家】五、代測數(shù)據(jù)詳細(xì)內(nèi)容
1、ELISA標(biāo)準(zhǔn)曲線;
2、實(shí)驗(yàn)具體詳細(xì)步驟;
3、完整的實(shí)驗(yàn)報(bào)告(試劑耗材,實(shí)驗(yàn)方法,實(shí)驗(yàn)結(jié)果及結(jié)果說明);
4、實(shí)驗(yàn)進(jìn)行階段,我公司客服人員會及時(shí)向您匯報(bào)實(shí)驗(yàn)進(jìn)程。
9238888 PCB, Main-01, BS96 CNY
9238886 Cable, HM, BS96 CNY 【人合胞病毒(RSV)IGMELISA試劑盒廠家】
9238854 #BR M96, Basic Agreement The Basic Cover Agreement M96 provides full service coverage for the BioRobot M96. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY
9238842 RS232 box, non-online fill, RapidPlate CNY
9241215 Full Agreement Depot Repair, Shaker, 1yr "The Full Agreement Depot Repair, Shaker provides full service coverage for the plate shaker used in the digene HPV application. 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
9238833 #BR 9604, Basic Agreement The Basic Cover Agreement 9604, 1 PM provides full service coverage for the BioRobot 9604. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY
9238832 BR 9600, Basic Agreement The Basic Cover Agreement 9600 provides full service coverage for the BioRobot 9600. Costs for service visits are fully covered including travel, labor, and parts. The agreement also includes one annual preventive maintenance visit, with costs for labor and parts covered. With a Basic Cover Agreement, the response time is 5 working days. CNY
9238819 Rect. carrier for 5 glass tubes 25ml CNY
9237527 Software LiquiChip Workstation IS V2.2. CNY
9237380 Installation, BR MDx & 2 react. setup Installation and training, including two customized reaction setup protocols CNY
9237379 Installation, BR MDx & 1 react. setup Installation and training, including one customized reaction setup protocol CNY
9237378 BR MDx, Installation The Installation, BR MDx facilitates the quick implementation of the BioRobot MDx into the lab routine by minimizing the instrument start-up phase. It covers the hardware and software installation of the BioRobot MDx instrument and provides the user with an introductory training on operation and user maintenance. The installation includes labor and travel costs. The performance of the installation process is documented on a GMP/GLP-compliant Field Service document. CNY
9237175 Guard Fan, Platic XYP CNY
9233209 Tubing, 3/2, CNY
9233155 Power Cord, European CNY
9236418 Board, CPU, TWI CNY
9236345 Red LSR CNY
9236166 Safety shield, RapidPlate CNY 【人合胞病毒(RSV)IGMELISA試劑盒廠家】
9230863 Anpressplatte Rose-80 CNY
9235538 Teaching Tool CNY
9230282 Cable, RS323, robot to syringe pump, 225 CNY
5050-2002 hc2 Software V2 Package CNY
BS96RNA BioSprint 96 to RNA (384) - UDP CNY
9240730 Tubing, 1/4" OD, Red, AP CNY
9240713 Poly Muffler Kit, AP96/196 CNY
9240690 Bearings, Lead Screws, AP CNY
9243654 Comprehen Valid., Other Quant. 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). For planning purposes and to ensure a smooth process, the Customer is expected to have all materials on-hand and inventoried one (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
6000-5013 LumiCheck Plate User Package CNY
288103 bactotype Mycoplasma Mg/Ms PCR Kit (24) CNY
1048147 QIAamp Viral RNA Mini Accessory Set CNY
270043 cattletype BHV1 gB Ab (5) CNY
QT-00005 福氏志賀氏菌(Shigellaflexneri)ATCC12022 凍干粉
QT-00006 表皮葡萄球菌ATCC12228 凍干粉
QT-00007 敗毒梭菌ClostridiumsepticumATCC12464 凍干粉
QT-00008 陰溝腸桿菌ATCC13047 凍干粉
QT-00009 產(chǎn)氣莢膜梭菌ATCC13124 凍干粉
QT-00010 熒光假單胞菌ATCC13525 凍干粉
QT-00011 嬰兒雙歧桿菌ATCC15697 凍干粉 【人合胞病毒(RSV)IGMELISA試劑盒廠家】
QT-00012 短雙歧桿菌ATCC15700 凍干粉
QT-00013 青春雙歧桿菌ATCC15703 凍干粉
QT-00014 黑曲霉ATCC16404 凍干粉
QT-00015 惡臭假單胞菌ATCC17485 凍干粉
QT-00016 單增李斯特氏菌ATCC19111 凍干粉
QT-00018 溶組織梭菌ClostridiumhistolyticumATCC19401 凍干粉
QT-00020 生孢梭菌ATCC19404 凍干粉
QT-00022 破傷風(fēng)桿菌/梭菌ClostridiumtetaniATCC19406 凍干粉
QT-00024 化膿性鏈球菌ATCC19615 凍干粉
QT-00025 黃桿菌屬ATCC21047 凍干粉
QT-00026 近平滑念珠菌ATCC22019 凍干粉
QT-00027 變異鏈球菌ATCC25175 凍干粉
QT-00028 脆弱擬桿菌ATCC25285 凍干粉
QT-00029 洋蔥假單胞菌ATCC25416 凍干粉
QT-00030 大腸埃希氏菌ATCC25922 凍干粉
QT-00032 金黃色葡萄球菌ATCC25923 凍干粉 【人合胞病毒(RSV)IGMELISA試劑盒廠家】
QT-00034 宋內(nèi)氏志賀氏菌(Sh.sonnei)ATCC25931 凍干粉
QT-00035 金黃色葡萄球菌ATCC27217 凍干粉
QT-00037 創(chuàng)傷弧菌ATCC27562 凍干粉
QT-00038 銅綠假單胞桿菌(綠膿桿菌)ATCC27853 凍干粉
QT-00040 糞腸球菌ATCC29212 凍干粉
QT-00041 金黃色葡萄球菌ATCC29213 凍干粉
QT-00047 兩歧雙歧桿菌ATCC29521 凍干粉
QT-00049 多形擬桿菌ATCC29741 凍干粉
QT-00051 糞腸球菌ATCC33186 凍干粉
QT-00053 空腸彎曲菌ATCC33291 凍干粉