情色五月天开心网,六月丁香小视频

您好，歡迎來到拜力生物網(wǎng)站！請登錄注冊

我的訂單 | 聯(lián)系我們 | 在線客服QQ：3012681483 | 客服電話：400-968-7988 | 工作時間：08:30-17:30

主營產(chǎn)品： ELISA試劑盒、抗體、補體血清、兔補體、干擾素、小鼠測溫儀、進(jìn)口試劑、Quidel代理、Swant代理、PBL Assay Science代理

網(wǎng)站首頁產(chǎn)品中心代理品牌新聞資訊資源中心關(guān)于我們

所在位置：首頁 > 產(chǎn)品中心 > abmgood > abmgood產(chǎn)品

Zebrafish Testicular Feeder Cells (ZtA6-1)

訂購信息

上海拜力生物科技公司

Tel:400-968-7988 021-33779008

Zebrafish Testicular Feeder Cells (ZtA6-1)

品牌：Abmgood

貨號：T2600

規(guī)格：

貨期：

應(yīng)用：

咨詢客服

立即購買加入購物車

Zebrafish Testicular Feeder Cells (ZtA6-1)

商品詳情參考文獻(xiàn) 相關(guān)資料

	Print Version
Safety	BioSafety Level II
Organism	Albino-type (alb-1/alb-1) zebrafish (Danio rerio)
Source Organ	Testis
Growth Properties	Adherent
Morphology	Epithelial and fibroblast-like
Applications	For Research Use Only.
Picture
Picture
Picture
Description	ZtA6 cells are derived from spontaneous tumor-like hypertropheied testis isolated from albino-type (alb-1/alb-1) zebrafish. Clones were analyzed for the expression of the Sertoli cell marker (Sox9a), the germ cell marker (Vas), and the Wilm’s tumor suppressor marker (WT1). 12 clones were derived and have distinctive properties and are available at abm. ZtA6-1 is clone 1 out of 12 derived from the ZtA6 zebrafish testicular cells. ZtA6-1 cells are unique in which there is an absence of Sox9a expression, but expresses WT1 marker, and has phagocytic activity. It is a valuable tool to study the testicular cells in a zebrafish model. Additionally, this cell line may be mitomycin C-treated to be co-cultured with male germ cells to support spermatogenesis.
Quality Control	1) Phagocytic activity was analyzed via the ability to internalize polystyrene beads; 2) RT-PCR was used to assess the presence or absence of WT1, Vas, and Sox9a markers; 3) Functionality test was performed to determine the ability to support male germ cells when co-cultured as feeder cells.
Propagation	Grow cells in T25 gelatin-coated flasks (TM063) with the following conditions. The base medium for this cell line is L-15 medium (ThermoFisher Scientific). To make the completed growth medium, add the following components to the base medium at the following final concentrations: 5 IU/ml human chorionic gonadotropin (Sigma), 2 IU/ml pregnant mare’s serum gonadotropin (Sigma), 0.2 mg/ml L-arginine (Gibco BRL), 0.02 mg/ml L-aspartic acid (Gibco BRL), 0.015 mg/ml L-histidine (Gibco BRL), 0.0725 mg/ml L-lysine HCl (Gibco BRL), 0.02 mg/ml L-proline (Gibco BRL), 0.5% bovine serum albumin (5% w/v stock solution, BSA fraction V, Sigma), 1% Hepes (Sigma), 3% fetal bovine serum (TM999), and 1% Penicillin/Streptomycin (G255). Atmosphere: air: 100%, Temperature: 28.0°C. To prepare as feeder cells: Treat with 10 μg/ml mitomycin C in L-15 for 5 hours before plating for use as feeder cells for further experimentation.
Storage	-180°C
Shipping	On Dry Ice
Notes	For Research Use Only, not for therapeutic or diagnostic purposes.