国产精品乱视频,国产精品va久久久久久久,2021国产精品视频网站,91久久成人免费,乱色熟女少妇一区二区,天天干夜夜操夜夜操,麻豆久久樱花一区二区av,国产高清久久久久

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 > EpH4 1424.1
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
EpH4 1424.1
EpH4 1424.1
規(guī)格:
貨期:
編號:B230243
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 EpH4 1424.1
商品貨號 B230243
Organism Mus musculus, mouse
Tissue breast epithelium (mammary gland); derived from metastatic site: kidney
Cell Type epithelial cell
Product Format frozen
Morphology epithelial-like
Culture Properties adherent
Biosafety Level 2

[Cells contain CMV and SV40 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.

Disease breast cancer
Gender female
Applications This cell line stably expresses constitutively activated form of MEK1 (Asp218/Asp222 MEK1 phosphorylation site mutant) and can be used in MEK-MAPK pathway studies. 

This cell line is tumorigenic, and can be used to study a breast cancer in vivo model

This cell line was derived from metastatic tumor and can be used to study breast cancer metastasis.

Storage Conditions liquid nitrogen vapor phase
Derivation EpH4 1424.1 was derived from BALB/c mouse xenografts initiated with EpH4 cells stably transfected with an expression vector containing Glu-Glu epitope-tagged phosphorylation site MEK1 mutant (MEKDD).  Cells were rederived from a metastatic tumor to the kidney after selection with 1 mg/mL G418 in complete medium.
Genes Expressed Constitutively activated form of MEK1, expressed
Cellular Products

stably expresses Glu-Glu tagged MEKDD, which is a constitutively activated form of MEK1 (Asp218/Asp222 MEK1 phosphorylation site mutant)

Tumorigenic Yes
Comments

EpH4 1424.1 was derived from BALB/c mouse xenografts initiated with EpH4 cells stably transfected with an expression vector containing Glu-Glu epitope-tagged phosphorylation site MEK1 mutant (MEKDD).  Cells were rederived from a metastatic tumor to the kidney after selection with 1 mg/mL G418 in complete medium.

Activation of MEK1 is mediated through phosphorylation of Ser218 and Ser222 by members of the Raf family of kinases. 

This cell line stably expresses constitutively activated form of MEK1(MEKDD), and can be used in MEK-MAPK pathway studies. 

This cell line was derived from metastatic tumor and can be used to study breast cancer metastasis. 

There are four additional related cell lines: B-MEKDD 116 cell line (ATCC CRL-3069), EpH4 1424 cell line (ATCC CRL-3071), EpH4 1424.2 cell line (ATCC CRL-3210) and EpH4-Ev cell line (ATCC CRL-3063). The EpH4 1424.1 cell line produces the constitutively activated MEK1 mutant MEKDD which has been tagged with Glu-Glu, verified at ATCC.

Complete Growth Medium The base medium for this cell line is ATCC-formulated DMEM Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium:
  • 10% Bovine Calf Serum
  • 1.2 mcg/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 1.0 to 2.0 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. An inoculum of 4 x 103 to 8 x 103 viable cells/cm2 is recommended.
  6. Incubate cultures at 37°C. Subculture when the cell concentration is between 8 x 104 to 1.5 x 105 cells/cm2.

Subcultivation ratio: A subcultivation ratio of 1:6 to 1:15 is recommended.
Medium renewal: Every 2 to 3 days
Culture Conditions Temperature: 37°C
Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Name of Depositor P Leder
References

Pinkas J, et al. MEK1 signaling mediates transformation and metastasis of EpH4 mammary epithelial cells independent of an epithelial to mesenchymal transition. Cancer Res. 62(16): 4781-90. PubMed: 12183438

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
万宁市| 定兴县| 汪清县| 海原县| 许昌县| 阳城县| 安达市| 阳城县| 呼图壁县| 大方县| 临武县| 文成县| 云和县| 四平市| 随州市| 莎车县| 田林县| 突泉县| 平陆县| 黄浦区| 和平区| 北辰区| 遂昌县| 通州市| 瑞安市| 永泰县| 西安市| 平凉市| 金塔县| 毕节市| 化隆| 宝丰县| 玉龙| 株洲县| 虎林市| 库伦旗| 宜州市| 阿拉善盟| 沭阳县| 任丘市| 古浪县|