人妻少妇偷人精品无码丨色婷婷av久久久久久久丨欧美xxxx做受性欧美88丨欧洲女人牲交视频免费丨亚洲精品久久久av无码专区

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(dāng)前位置: 首頁 > ATCC代理 > MC3T3-E1 Subclone 14
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(hào)
  • 創(chuàng)e慧谷42號(hào)樓B幢401室
MC3T3-E1 Subclone 14
MC3T3-E1 Subclone 14
規(guī)格:
貨期:
編號(hào):B162184
品牌:Mingzhoubio

標(biāo)準(zhǔn)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 MC3T3-E1 Subclone 14
商品貨號(hào) B162184
Organism Mus musculus, mouse
Tissue bone, calvaria
Cell Type preosteoblast
Product Format frozen
Morphology fibroblast
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.

Age newborn
Strain C57BL/6
Applications
These cell lines are good models for studying in vitro osteoblast differentiation, particularly ECM signaling. They have behavior similar to primary calvarial osteoblasts.
Storage Conditions liquid nitrogen vapor phase
Derivation
A series of subclones were isolated from the cloned but phenotypically heterogeneous MC3T3-E1 cell line.
Genes Expressed
collagen
Cellular Products
collagen
Tumorigenic Yes
Effects
Yes, in immunodeficient mice
Comments

The subclones were selected for high or low osteoblast differentiation and mineralization after growth in medium containing ascorbic acid.

The MC3T3-E1 Subclone 4 (ATCC CRL-2593) and the MC3T3 Subclone 14 (ATCC CRL-2594) lines exhibit high levels of osteoblast differentiation after growth in ascorbic acid and 3 to 4 mM inorganic phosphate.

They form a well mineralized extracellular matrix (ECM) after 10 days.

The MC3T3 Subclone 24 (ATCC CRL-2595) and the MC3T3 Subclone 30 (ATCC CRL-2596) lines exhibit poor osteoblast differentiation after growth in ascorbic acid. They do not form ECM. They can be used as negative controls for Subclones 4 and 14.Mineralizing subclones selectively express mRNAs for the osteoblast markers, bone sialoprotein (BSP), osteocalcin (OCN), and the parathyroid hormone (PTH)/parathyroid hormone-related protein (PTHrP) receptor.

Subclones with both high and low differentiation potential produce similar amounts of collagen in culture and express comparable basal levels of mRNA encoding Osf2/Cbfa1, an osteoblast-related transcription factor.
After implantation into immunodeficient mice, highly differentiating subclones form bone-like ossicles resembling woven bone, while poorly differentiating cells only produce fibrous tissue.
Complete Growth Medium The base medium for this cell line is Alpha Minimum Essential Medium with ribonucleosides, deoxyribonucleosides, 2 mM L-glutamine and 1 mM sodium pyruvate, but without ascorbic acid (GIBCO, Custom Product, Catalog No. A1049001). 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 0.25% (w/v) Trypsin-0.53% (w/v) EDTA solution to remove all traces of serum that contains trypsin inhibitor.
  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

Subculture Ratio: 1:6 to 1:8
Medium Renewal: Every 2 to 3 days.
Note: For more information on enzymatic dissociation and subculturing of cell lines consult Chapter 10 in Culture of Animal Cells, a manual of Basic Technique by R. Ian Freshney, 3rd edition, published by Alan R. Liss, N.Y., 1994

Cryopreservation
Freeze medium: Complete growth medium 95%; DMSO, 5%
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Temperature: 37°C
Name of Depositor RT Franceschi
Deposited As mouse
References

Wang D, et al. Isolation and characterization of MC3T3-E1 preosteoblast subclones with distinct in vitro and in vivo differentiation/mineralization potential. J. Bone Miner. Res. 14: 893-903, 1999. PubMed: 10352097

forms bone-like ossicles

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
主站蜘蛛池模板: 日本vs亚洲vs韩国一区三区| 春色校园综合人妻av| 成人麻豆日韩在无码视频| 亚洲精品欧美综合一区二区| 99久久久国产精品消防器材| 日本一区二区三区免费高清| 国内精品伊人久久久久777| 午夜福利精品亚洲不卡| 777午夜福利理伦电影网| 无码国产色欲xxxxx视频| 亚洲中文字幕无码一区二区三区| 超清中文乱码字幕在线观看| 精产国品一区二区三产区| 午夜成人无码片在线观看影院| 亚洲国产欧美日韩在线人成| 精品国产青草久久久久福利| 国产熟睡乱子伦午夜视频| 掀开奶罩边吃边摸下娇喘视频| 天堂а√中文在线| 久久97久久97精品免视看| 可以直接免费观看的av网站| 欧美人与动牲交zooz乌克兰| 东京热毛片无码dvd一二三区| 国精产品48x国精产品| 最新av偷拍av偷窥av网站| 国产69精品久久久久777| 免费国产成人高清在线视频 | 女人被躁到高潮免费视频| 久久综合给久久狠狠97色| 欧美一区二区三区成人片在线| 日本丰满熟妇bbxbbxhd| 日韩69永久免费视频| 欧美性受xxxx白人性爽| 国产96在线 | 欧美| 青青青国产在线观看资源| 97久久精品人人槡人妻人| 爆乳熟妇一区二区三区霸乳| 天美传媒精品1区2区3区| 亚洲精品国产av现线| 国产av国片精品| 在线中文新版最新版在线 |