亚洲精品无码成人片久久不卡,亚洲自偷自偷在线传媒,亚洲精品在线,久久无码精品九号,欧洲av人人爽爽,亚洲精品蜜桃久久久久久,亚洲精品久久午夜无码专区电影,辽宁少妇高潮45分钟,少妇高清性色生活片,无码八少妇久久

熱門搜索:A549    293T 金黃色葡萄球菌 大腸桿菌 AKK菌
購物車 1 種商品 - 共0元
當前位置: 首頁 > ATCC代理 > CHO-CD36
最近瀏覽歷史
聯(lián)系我們
  • 0574-87157013
  • mingzhoubio@163.com
  • 浙江省寧波市鎮(zhèn)海區(qū)莊市街道興莊路9號
  • 創(chuàng)e慧谷42號樓B幢401室
CHO-CD36
CHO-CD36
規(guī)格:
貨期:
編號:B164252
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 CHO-CD36
商品貨號 B164252
Organism Cricetulus griseus, hamster, Chinese
Tissue ovary
Product Format frozen
Morphology epithelial
Culture Properties adherent
Biosafety Level 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Gender female
Applications
The cells can be used in adherence assays as a target cell for malaria infected erythrocytes.
Functional expression of the transfected receptor molecules on CHO-CD36 was confirmed using parasites with different cytoadherence phenotypes and cytoadherence inhibition experiments with a panel of anti-CD36 antibodies.
The use of isolates obtained from malaria patients in The Gambia confirmed the applicability of using these cells in assays for laboratory studies.
Storage Conditions liquid nitrogen vapor phase
Derivation
The CHO-CD36 cell line was constructed at DNAX Research Institute, Palo Alto, California by transfecting Chinese hamster ovary (CHO) cells with linearized cDNA of human CD36 in pCDM8 by electroporation in a 10 fold molar excess over pBJ1-Neo.
The use of isolates obtained from malaria patients in The Gambia confirmed the applicability of using these cells in assays for laboratory studies.
Clinical Data
The use of isolates obtained from malaria patients in The Gambia confirmed the applicability of using these cells in assays for laboratory studies.
female
Comments
The CHO-CD36 cell line was constructed at DNAX Research Institute, Palo Alto, California by transfecting Chinese hamster ovary (CHO) cells with linearized cDNA of human CD36 in pCDM8 by electroporation in a 10 fold molar excess over pBJ1-Neo.
Stable transfectants were then selected by growth in culture medium containing G418.
CHO-CD36 cells express high levels of human CD36 (a ligand for erythrocytes infected with the human malaria parasite, Plasmodium falciparum).
The cells can be used in adherence assays as a target cell for malaria infected erythrocytes.
Functional expression of the transfected receptor molecules on CHO-CD36 was confirmed using parasites with different cytoadherence phenotypes and cytoadherence inhibition experiments with a panel of anti-CD36 antibodies.
The use of isolates obtained from malaria patients in The Gambia confirmed the applicability of using these cells in assays for laboratory studies.
A culture submitted to the ATCC in August 1993 was found to be contaminated with mycoplasma, and the line was cured by a 21 day treatment with BM Cycline.
Complete Growth Medium The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, Catalog No. 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing Volumes used in this protocol are for 75 cm2 flask; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS) or 0.25%Trypsin-0.53mM EDTA solution.
  3. Add 2.0 to 3.0 mL of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes).
    Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal.
  4. Add 6.0 to 8.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Add appropriate aliquots of the cell suspension to new culture vessels.
  6. Incubate cultures at 37°C.

Subcultivation Ratio: 1:6 to 1:10
Medium Renewal: Every 2 to 3 days

Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 13 in Culture of Animal Cells, a Manual of Basic Technique by R. Ian Freshney, 5th edition, published by Wiley-Liss, N.Y., 2005.

Cryopreservation

Complete growth medium described above supplemented with 5% (v/v) DMSO.  Cell culture tested DMSO is available as ATCC Catalog No. 4-X.

Culture Conditions
Temperature: 37°C
Atmosphere: Air, 95%; Carbon dioxide (CO2), 5%
梅經(jīng)理 17280875617 1438578920
胡經(jīng)理 13345964880 2438244627
周經(jīng)理 17757487661 1296385441
于經(jīng)理 18067160830 2088210172
沈經(jīng)理 19548299266 2662369050
李經(jīng)理 13626845108 972239479
三原县| 赫章县| 聊城市| 浮山县| 寻乌县| 益阳市| 武平县| 盐亭县| 丹东市| 青阳县| 怀远县| 寻乌县| 读书| 河西区| 广安市| 吉木萨尔县| 即墨市| 东阳市| 临沧市| 玉门市| 永顺县| 忻城县| 云林县| 双柏县| 托克托县| 商城县| 涞水县| 彭山县| 通海县| 出国| 高要市| 盘锦市| 钟山县| 理塘县| 织金县| 宜黄县| 商南县| 宾阳县| 宣汉县| 建德市| 遂川县|