999久久久国产精品,国产情侣一区二区,亚洲AV中文无码乱人伦在线视色,国产欧美一区二区三区在线看,欧美一区精品视频一区二区,色老头在线一区二区三区,又大又粗又硬又爽又黄毛片,国产98在线免费

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 > hTERT-HPNE E6/E7/K-RasG12D
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
hTERT-HPNE E6/E7/K-RasG12D
hTERT-HPNE E6/E7/K-RasG12D
規(guī)格:
貨期:
編號:B241993
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


產品名稱 hTERT-HPNE E6/E7/K-RasG12D
商品貨號 B241993
Organism Homo sapiens, human
Tissue pancreas, duct
Product Format frozen
Morphology epithelial-like
Culture Properties adherent
Biosafety Level 2  [Cells contain Human Papilloma (HPV16) viral DNA sequences]

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 52 years
Gender male
Storage Conditions liquid nitrogen vapor phase
Karyotype This is a pseudodiploid human cell line of male origin. Clonal aberrations included the derivative chromosomes: t(3;18)(p21;q11.2) [balanced translocation], del(6)(q15), add(8)(q11.2) and der(21)t(17;21)(q21;p11.2). The percentage of cells with the normal male chromosome complement increased at high passage and non-clonal aberrations were seen in approximately 20% of the examined cells at all passages.
Derivation
Method: developed by infection of hTERT-HPNE E6/E7 cells (ATCC CRL-4036) with retroviral vector (pLXSN) carrying a G12D mutant of the isoform b of human K-Ras
Clinical Data
male
Antigen Expression
positive for nestin (flow cytometry) (verified at ATCC)
Genes Expressed
positive for nestin (flow cytometry)(verified at ATCC)
Tumorigenic NO
Complete Growth Medium The base medium for this cell line is:
  • 75% DMEM without glucose (Sigma Cat#. D-5030 with additional 2 mM L-glutamine and 1.5 g/L sodium bicarbonate)
  • 25% Medium M3 Base (Incell Corp. Cat# M300F- 500)
To make the complete growth medium, add the following components to the base medium:
  • fetal bovine serum 5% (final conc.)
  • 10 ng/ml human recombinant EGF
  • 5.5 mM D-glucose (1g/L)
  • 750 ng/ml puromycin

Subculturing
Volumes used in this protocol are for 75 cm2 flasks; 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% (w/v) Trypsin - 0.53 mM EDTA solution to remove all traces of serum which 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 2.0 to 3.0 mL of complete growth medium and aspirate cells by gently pipetting.
  5. Transfer cell suspension to a centrifuge tube and spin at approximately 125 X g for 5 to 10 minutes. Discard supernatant.
  6. Resuspend the cell pellet in fresh growth medium. Add appropriate aliquots of the cell suspension to new culture vessels. An inoculum of 4 X 103 to 6 X 103 viable cells/cm2 is recommended.
  7. Incubate cultures at 37°C. Subculture when cell density reaches between 5 X 104 and 6 X 104 cells/cm2.
Subcultivation ratio: 1:8 to 1:12 twice weekly
Medium renewal: every 2 to 3 days
Cryopreservation
Freeze medium: fetal bovine serum (FBS), 90%; DMSO, 10%
Storage temperature: liquid nitrogen vapor phase
Culture Conditions
Temperature: 37°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
STR Profile
CSF1PO: 12
D13S317: 12, 13
D16S539: 12, 13
D5S818: 11
D7S820: 9, 10
TH01: 8, 9
TPOX: 8, 11
vWA: 17
Amelogenin: XY
Population Doubling Level (PDL)

Longevity: >15 PDLs post-cryopreservation recovery

Population Doubling Time approximately 29 hours
Name of Depositor M Ouellette
Year of Origin July 2002
References

Lee KM. et al. Immortalization with telomerase of the Nestin-positive cells of the human pancreas. Biochem. Biophys. Res. Commun. 301(4):1038-1044, 2003. Pubmed: 12589817

Lee KM. et al. Notch2-positive progenitors with the intrinsic ability to give rise to pancreatic ductal cells. Lab. Invest. 85 (8): 1003-1012, 2005. Pubmed: 15924149

Campbell PM, et al. K-Ras promotes growth transformation and invasion of immortalized human pancreatic cells by Raf and phosphatidylinositol 3-kinase signaling. Cancer Res. 67(5): 2098-2106, 2007. PubMed: 17332339

Campbell PM, et al. Ras-driven transformation of human nestin-positive pancreatic epithelial cells. Methods Enzymol. 439: 451-465, 2008. PubMed: 18374182

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
景宁| 屯留县| 施甸县| 上杭县| 景洪市| 墨竹工卡县| 建湖县| 贡山| 古田县| 措美县| 崇阳县| 大同县| 麻江县| 汽车| 繁峙县| 济南市| 湖北省| 五华县| 商洛市| 玉山县| 毕节市| 凤凰县| 儋州市| 额济纳旗| 达日县| 蚌埠市| 无极县| 丽水市| 类乌齐县| 油尖旺区| 阿拉善盟| 沾化县| 临泉县| 陈巴尔虎旗| 湘潭市| 怀仁县| 易门县| 沈阳市| 丹东市| 册亨县| 丘北县|