您好,欢迎来到仪表展览网!
请登录
免费注册
分享
微信
新浪微博
人人网
QQ空间
开心网
豆瓣
会员服务
进取版
标准版
尊贵版
|
设为首页
|
收藏
|
导航
|
帮助
|
移动端
|
官方微信扫一扫
微信扫一扫
收获行业前沿信息
产品
资讯
请输入产品名称
噪声分析仪
纺织检测仪器
Toc分析仪
PT-303红外测温仪
转矩测试仪
继电保护试验仪
定氮仪
首页
产品
专题
品牌
资料
展会
成功案例
网上展会
词多 效果好 就选易搜宝!
上海乾思生物科技有限公司
新增产品
|
公司简介
注册时间:
2017-10-17
联系人:
电话:
Email:
首页
公司简介
产品目录
公司新闻
技术文章
资料下载
成功案例
人才招聘
荣誉证书
联系我们
产品目录
sigma现货
试剂盒
细胞库
美国ATCC
当前位置:
首页
>>>
产品目录
>>>
美国ATCC
仪表展览网
>>>
展馆展区
>>>
MyC-CaP Mus musculus│prostate
>
MyC-CaP Mus musculus│prostate
产品资料
MyC-CaP Mus musculus│prostate
如果您对该产品感兴趣的话,可以
产品名称:
MyC-CaP Mus musculus│prostate
产品型号:
产品展商:
乾思生物中心
产品文档:
无相关文档
简单介绍
MyC-CaP Mus musculus│prostate
产品描述
ATCCCRL-3255 MyC-CaP
基本信息
资源名称
MyC-CaP
种属
Mus musculus
prostate
形态
epithelial-like
提供形式
frozen
致病类型
prostate cancer
**等级
1
应用领域
Study of prostate cancer progression from androgen dependence to a hormone-refractory or androgen-independent stage
培养方法
培养基
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%.
传代方法
Volumes used in this protocol are for 75 cm2 flasks; proportionally reduce or increase amount of dissociation medium for culture vessels of other sizes. Remove and discard culture medium. Briefly rinse the cell layer with Ca++/Mg++ free Dulbecco's phosphate-buffered saline (D-PBS) (ATCC® 30-2200) or 0.05% Trypsin – 0.02% EDTA for Primary Cells (ATCC® PCS-999-003) solution to remove all traces of serum which contains trypsin inhibitor. 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. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting. Transfer cell suspension to a centrifuge tube and spin at approximately 125 x g for 5 to 10 minutes. Discard supernatant. Resuspend the cell pellet in fresh growth medium. Add appropriate aliquots of the cell suspension to new culture vessels. Incubate cultures at 37°C. Subcultivation ratio: 1:5 to 1:20 is recommended.
Medium renewal: 2 to 3 times a week
生长条件
Temperature: 37°C Atmosphere: air, 95%; carbon dioxide (CO2), 5%
生长特性
adherent
存储条件
liquid nitrogen vapor phase;complete growth medium, 90%; DMSO, 10%
详细说明
描述
The cells have an amplified androgen receptor gene despite no prior exposure to androgen withdrawal. These cells express wild-type androgen receptor (AR), retain androgen-dependent transgene expression and demonstrate androgen-dependent growth on soft agar and in mice.
Age
16 months
Gender
male
Strain
FVB; Hi-Myc transgenic
Derivation
The MyC-CaP cell line was derived from a genetically engineered mouse prostate cancer removed from an animal that was never exposed to hormone ablation.
Receptor Expression
wild-type androgen receptor (AR)
Seeding Density
5 x103 to 1 x 104 viable cells/cm2
Population Doubling Time
18 hours
Year of Origin
2005
Restrictions
This product's use is governed by the MTA and the following Contributor Rights (1) Contributor will be informed of all customers that purchase this product; (2) For information on executing a license to use this product for research use (for-profit entities) or Commercial·Use (for-profit and non-profit entities); contact UCLA Office of Intellectual Property at 310-794-0558 or innovation@research.ucla.edu.
产品留言
标题
联系人
联系电话
内容
验证码
点击换一张
注:1.可以使用快捷键Alt+S或Ctrl+Enter发送信息!
2.如有必要,请您留下您的详细联系方式!
温馨提示:为规避购买风险,建议您在购买前务必确认供应商资质与产品质量。
免责申明:以上内容为注册会员自行发布,若信息的真实性、合法性存在争议,平台将会监督协助处理,
欢迎举报
产品留言
标题
内容
联系人
联系电话
电子邮件
公司名称
联系地址
验证码
点击换一张
注:1.可以使用快捷键Alt+S或Ctrl+Enter发送信息!
2.如有必要,请您留下您的详细联系方式!
相关产品
CA46 Homo sapiens, human│
TC1 Mus musculus (B cell); Mus musculus (myeloma), mouse (B cell); mouse (myelo
VMM5A 人黑色素瘤细胞
Dubca Camelus dromedarius, camel│skin
Dubca Camelus dromedarius, camel│skin
若网站内容侵犯到您的权益,请通过网站上的联系方式及时联系我们修改或删除