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齐一生物科技(上海)有限公司

产品介绍

人结肠微血管内皮细胞

价 格:¥电议

型 号:

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生产地:其他访问量:18次

发布日期:2016/6/25 22:15:35

更新日期:2016/6/25 22:15:35

详细内容

 人结肠微血管内皮细胞齐一生物科技(上海)有限公司产品已被广泛应用于化学、化工、生命科学的基础研究和开发应用、制药、疾病诊断与控制、人口与健康、生物技术等诸多领域.客户遍布国内各大学、研究所、医院、卫生防疫、商品检验检疫、制药公司、生物技术公司和食品工业等单位. 齐一生物销售:0216034 8496181214 53965173021 04490Web:www.qiyibio.com

人结肠微血管内皮细胞下面是细胞株培养的具体无菌技术要点:

1. 实验开始前,无菌室和无菌操作台需要紫外光照射3060分钟完全灭菌,用70%ethanol擦拭无菌操作台面,并且打开无菌操作台风扇运行10分钟之后,才可以进行实验操作。每次操作只能处理一株细胞株,即使培养基完全相同也不可共用培养基,以避免细胞间污染或失误混淆。实验完成后,请将实验物品拿出工作台,用70%ethanol再次擦拭无菌操作台面。操作间隔应该让无菌操作台运转10分钟到15分钟后,才能进行下一个细胞株的操作。

2. 无菌操作工作的区域应保持清洁和宽敞,必要物品(试管架、吸管、吸取器或吸管盒等)可以暂时放置,其它实验用品使用完毕后应移出,有利于空气流通。实验用品需70%ethanol擦拭后方可带入无菌操作台内。实验操作过程应在台面的中央无菌区域内完成,请勿在边缘非无菌区域进行操作。

3. 小心取用无菌实验物品,避免细菌污染。请勿触碰吸管尖头部和容器瓶口处,也不要在打开的容器正上方进行操作。容器打开后,请用手夹住瓶盖并轻握瓶身,倾斜大约45°角取用,尽量不要将瓶盖口朝上放置于桌面。

4. 工作人员应当首先注意自身安全,必须穿戴齐实验衣和实验手套后才能进行实验。对于病毒感染或是来自人类的细胞株应当特别小心操作,并选择适当等级的无菌操作台进行(至少是Class II)。操作过程中,应避免引起aerosol的产生,小心有毒性药品,例如DMSOTPA等,并避免针头的伤害等等。

5. 定期检测下列项目:

5.1. CO2钢瓶的CO2压力

5.2. CO2培养箱的CO2浓度、温度、和水盘是否有污染(水盘的水需用无菌水,每周定时更换)。

5.3. 无菌操作台内的airflow压力,定期更换紫外线灯管和HEPA过滤膜,预滤网(300小时/预滤网,3000小时/HEPA)。

6. 水槽内可添加消毒剂(Zephrin 1:750),需定期更换水槽中的水。

 

人结肠微血管内皮细胞齐一生物友情提醒,本产品仅供科研使用,不得用于临床及诊断使用!

一细胞说明,具体详细请见细胞附带说明书

 二、客户自备试剂

1、PBS  

2、 2RPMI-1640 培养基(不含 Hepes+ 10%胎牛血清+ 1%双抗

30.25%  W/V)胰蛋白酶(含 0.02% EDTA

三、细胞背景

1、生长方式:贴壁

2、种属:Homo sapiens 

四、培养条件

1、培养基:RPMI-1640 培养基(不含 Hepes+ 10%胎牛血清+ 1%双抗

2、温度:37.0°C

3、气体:空气  95%CO2 5%

人结肠微血管内皮细胞五、培养方法

 收到细胞后,在倒置显微镜下观察整个细胞生长情况:

 如果细胞未长满,用 75%酒精喷洒整个瓶消毒后放到超菌台内,严格无菌操作,打开细胞培养瓶,留10ml 培养液继续培养。如果细胞已长满(达 80-90%)。即可进行传代,具六、体步骤如下:

1,弃去培养液,用PBS 1-2次。

2,向瓶内加入 1.0-2.0ml 胰蛋白酶液,在倒置显微镜下观察细胞消化情况,若细胞大部分变圆,迅速拿回操作台,吸取胰蛋白酶,加含有 6ml  10%血清的培养液,轻轻吹打细胞。

3,加入等量的的培养液,轻轻吹打混匀后吸出一半,分到新的培养

4,传代比例:1:2-1:3  

七、常见问题及解决方案

1、培养瓶有破裂,培养液有漏液:细胞极大可能会污染,所以我们会及时安排帮老师解决。

2、细胞漂浮:培养瓶不开封,瓶口酒精擦拭后平躺放置在培养箱。次日观察,如细胞大部分又贴回瓶底,表明细胞活力正常,剩余漂浮的细胞可以去掉,留 10ml 培养液培养观察,细胞生长至汇合度 80%,进行消化传代;如细胞还是不贴壁,将细胞离心收集转到新培养瓶,原培养瓶加部分培养液继续培养,中间注意观察,我们的技术人员会一直跟踪指导,直到问题解决。

 

细胞培养代理品牌

 

BD 产品涉及分子生物学、细胞生物学、免疫学和蛋白质组学等诸多领域,旗下拥有Clontech Discovery labware Pharmingen Falcon 等质品牌,值得称赞的是每一个品牌在其所在的领域都是其中的佼佼者。 
http://www.bdbiosciences.com/home.jsp

 

细胞培养代理品牌

 

GIBCO 作为细胞培养的金字招牌,是在此领域的领导者,现在是Invitrogen的一部分。Gibco可以提供为广泛的品种以满足用户不同的需求,每一种产品都通过为严格的品质管理。同时,Gibco也可按客户的要求对培养基的配方进行改动,或完全按客户的配方进行生产。 
http://www.invitrogen.com/site/us/en/home.html

 

人结肠微血管内皮细胞齐一生物科技(上海)有限公司是一家专业生产和销售各种生化试剂,细胞株、原代细胞、菌种、医药中间体,标准品和对照品的大型化学科技公司. 齐一生物销售:0216034 8496181214 53965173021 04490Web:www.qiyibio.com

 

9238854#BR M96, Basic AgreementThe 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

9238842RS232 box, non-online fill, RapidPlateCNY

9241215Full 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 AgreementThe 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

9238832BR 9600, Basic AgreementThe 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

9238819Rect. carrier for 5 glass tubes 25mlCNY

9237527Software LiquiChip Workstation IS V2.2.CNY

9237380Installation, BR MDx & 2 react. setupInstallation and training, including two customized reaction setup protocolsCNY

9237379Installation, BR MDx & 1 react. setupInstallation and training, including one customized reaction setup protocolCNY

9237378BR MDx, InstallationThe 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

9237175Guard Fan, Platic XYPCNY

9233209Tubing, 3/2,CNY

9233155Power Cord, EuropeanCNY

9236418Board, CPU, TWICNY

9236345Red LSRCNY

9236166Safety shield, RapidPlateCNY

9230863Anpressplatte Rose-80CNY

9235538Teaching ToolCNY

9230282Cable, RS323, robot to syringe pump, 225CNY

5050-2002hc2 Software V2 PackageCNY

BS96RNABioSprint 96 to RNA (384) - UDPCNY

9240730Tubing, 1/4" OD, Red, APCNY

9240713Poly Muffler Kit, AP96/196CNY

9240690Bearings, Lead Screws, APCNY

9243654Comprehen 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

6000-5013LumiCheck Plate User PackageCNY

288103bactotype Mycoplasma Mg/Ms PCR Kit (24)CNY

1048147QIAamp Viral RNA Mini Accessory SetCNY

270043cattletype BHV1 gB Ab (5)CNY

1019992Buffer Set (RNeasy 96 BioRobot 9604 KitCNY

 

273401pigtype Toxoplasma Ab (1)CNY


QY-x1684人胚肺二倍体细胞CCC-HPF-1胚胎;肺DMEM+ 10% FBS
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QY-x1687人肝癌细胞Hep G2HB-8065?肝细胞癌DMEM+10%NBCS
QY-x1688人肝癌细胞BEL-7402肝癌RPMI 1640 + 10% NBCS
QY-x1689鼠肝癌细胞H22(悬浮)肝癌RPMI 1640 + 10% NBCS
QY-x1690人肺腺癌
QY-x1691人肺癌细胞SPC-A-1肺癌RPMI 1640 + 10% FBS
QY-x1692人肺癌细
QY-x1693人非小细胞肺癌细胞A549CCL-185?肺癌RPMI 1640 + 10% NBCS
QY-x1694人肺癌细胞GLC82肺癌
QY-x1695人小细胞肺癌细胞
QY-x1696人肺鳞癌细胞NCI-H446HTB-171?肺癌RPMI 1640 + 10% NBCS
QY-x1697人肺鳞癌细胞NC1-H460肺鳞癌RPMI 1640 + 10% FBS
QY-x1698鼠Lewis肺腺癌细胞(非小细胞)LLC肺癌RPMI 1640 + 10% FBS
QY-x1699人胃腺癌细胞(低分化)BGC-823胃癌RPMI 1640 + 10% NBCS
QY-x1700人胃癌细胞NCI-N87CRL-5822? 胃癌RPMI 1640 + 10% FBS
QY-x1701人胃癌细胞(未分化)HGC-27胃癌RPMI 1640 + 10% NBCS
QY-x1702人乳腺癌细胞MCF-7HTB-22?腺癌,乳腺,胸水。DMEM+10%NBCS
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QY-x1705人结肠癌细胞CaCo-2HTB-37?结肠癌DMEM+10%FBS
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QY-x1707人恶性黑色素瘤细胞A-375CRL-1619? 皮肤;恶性黑色素瘤DMEM+10%NBCS
QY-x1708鼠黑色素瘤细胞B16-luc黑色素瘤RPMI 1640 + 10% NBCS
QY-x1709人纤维肉瘤细胞HT1080CCL-121? 纤维肉瘤MEM或 DMEM+10%FBS
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QY-x1711人T淋巴细胞白血病细胞(悬浮)Jurkat E6-1TIB-152?T淋巴细胞;急性T细胞白血病RPMI 1640 + 10% FBS
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