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
當前位置: 首頁 > ATCC代理 > L6
最近瀏覽歷史
聯系我們
  • 0574-87157013
  • mingzhoubio@163.com
  • 浙江省寧波市鎮海區莊市街道興莊路9號
  • 創e慧谷42號樓B幢401室
L6
L6
規格:
貨期:
編號:B164949
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規格:
凍干粉
斜面
甘油
平板


產品名稱 L6
商品貨號 B164949
Organism Rattus norvegicus, rat
Tissue skeletal muscle
Cell Type myoblast
Product Format frozen
Morphology myoblast
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.

Applications
This cell line is a suitable transfection host.
Storage Conditions liquid nitrogen vapor phase
Images
Derivation
The L6 myogenic line was isolated originally by Yaffe from primary cultures of rat thigh muscle maintained for the first two passages in the presence of methyl cholanthrene.
Genes Expressed
myosin
Cellular Products
myosin
Comments
L6 cells fuse in culture to form multinucleated myotubes and striated fibers. The extent of cell fusion declines with passage and the cells should be frozen at low passage and periodically recloned with selection for fusion competent cells.
Tested and found negative for ectromelia virus (mousepox).
Complete Growth Medium The base medium for this cell line is ATCC-formulated Dulbecco's Modified Eagle's Medium, Catalog No. 30-2002. 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 are given for a 75 cm2 flask. Increase or decrease the amount of dissociation medium needed proportionally for culture vessels of other sizes. Subculture before the cells become confluent to retard the loss of differentiating ability that is observed as the cells are passaged. Corning® T-75 flasks (catalog #430641) are recommended for subculturing this product.
  1. Remove and discard culture medium.
  2. Briefly rinse the cell layer with 0.25% (w/v) Trypsin- 0.53 mM 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.
Subcultivation Ratio: A subcultivation ratio of 1:20 to 1:40 is recommended
Medium Renewal: 2 to 3 times per week
Note: The myoblastic component of this line will be depleted rapidly if the cells are allowed to become confluent.
Cryopreservation
Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37°C
Name of Depositor D Schubert
Deposited As Rattus sp.
Passage History
The L6 myogenic line was isolated originally by Yaffe from primary cultures of rat thigh muscle maintained for the first two passages in the presence of methyl cholanthrene.
L6 cells fuse in culture to form multinucleated myotubes and striated fibers. The extent of cell fusion declines with passage and the cells should be frozen at low passage and periodically recloned with selection for fusion competent cells.
References

Mandel JL, Pearson ML. Insulin stimulates myogenesis in a rat myoblast line. Nature 251: 618-620, 1974. PubMed: 4421831

Richler C, Yaffe D. The in vitro cultivation and differentiation capacities of myogenic cell lines. Dev. Biol. 23: 1-22, 1970. PubMed: 5481965

Yaffe D. Retention of differentiation potentialities during prolonged cultivation of myogenic cells. Proc. Natl. Acad. Sci. USA 61: 477-483, 1968. PubMed: 5245982

Osawa H, et al. Identification and characterization of basal and cyclic AMP response elements in the promoter of the rat hexokinase II gene. J. Biol. Chem. 271: 17296-17303, 1996. PubMed: 8663388

Osawa H, et al. Analysis of the signaling pathway involved in the regulation of hexokinase II gene transcription by insulin. J. Biol. Chem. 271: 16690-16694, 1996. PubMed: 8663315

Cross References

Nucleotide (GenBank) : M87067 R.norvegicus activin type IIB receptor mRNA.

Nucleotide (GenBank) : X57986 Rat mRNA for C alpha subunit of the cAMP-dependent protein kinase.

梅經理 17280875617 1438578920
胡經理 13345964880 2438244627
周經理 17757487661 1296385441
于經理 18067160830 2088210172
沈經理 19548299266 2662369050
李經理 13626845108 972239479
主站蜘蛛池模板: 国产乱子夫妻xx黑人xyx真爽| 国产高清色高清在线观看| 精品综合久久久久久98| 国产成人精品a视频| 午夜私人成年影院| 亚洲熟妇无码八v在线播放| av鲁丝一区鲁丝二区鲁丝三区| 国产伦精品一区二区三区免费迷| 国产人妻高清国产拍精品| 鲁一鲁一鲁一鲁一曰综合网 | 中文字幕人妻熟女人妻| 久久久久国产精品人妻| 久久精品av麻豆| 亚洲伊人久久精品酒店| 国产精品毛片无码| 久久婷婷五月综合色精品| 免费无遮挡很爽很污很黄的网站| 亚洲高清国产拍精品闺蜜合租| 国产精品沙发午睡系列| 久久人人爽人人爽人人片dvd| 免费无码午夜福利片69| 无码精品人妻一区二区三区湄公河 | 国产国拍精品av在线观看| 国内精品久久久久影院优| 一本久久知道综合久久| 亚洲妇女无套内射精| 午夜福利不卡在线视频| 国产高清在线精品一区免费| 老熟女高潮一区二区三区| 麻豆精品一卡二卡三卡| 亚洲色播永久网址大全| 欧美一区二区三区成人片在线| 国产xxxx做受性欧美88| 国产日韩在线视看高清视频手机| 老头边吃奶边弄进去呻吟| 无码人中文字幕| 337p亚洲日本中国大胆69| 男女下面一进一出无遮挡| 国产女人的高潮国语对白| 3d动漫精品啪啪一区二区中 | 真实国产乱啪福利露脸|