背景介紹/context：

iPSC (induced Pluripotent Stem cells) reprogrammed from human Fibroblasts of a Gaucher Syndrome (Morbus Gaucher) patient.This iPS cell line was created using a normal human fibroblast derived from tissue of a male infant suffering from Gaucher Syndrom (Morbus Gaucher). The iPS cell line was generated using an episomal reprogramming containing a prprietary mix of vectors, containing Oct-4, Sox-2, Klf-4 along with p53 Anti-sense, EBNA-1. The cell line was validated for pluripotency based on colony morphology, alkaline phosphatase expression, and expression of SSEA-4.iPS colonies exhibit classical morphology and growth.Absence of Mycoplasma was confirmed.The cell line is shipped on dry ice.

由戈謝氏綜合征(Morbus Gaucher)患者的人類成纖維細(xì)胞重編程的iPSC(誘導(dǎo)多能干細(xì)胞)。這一iPS細(xì)胞系是利用一個(gè)患有戈謝氏綜合征(Morbus Gaucher)男嬰的組織中提取的正常人類成纖維細(xì)胞創(chuàng)建的。iPS細(xì)胞系是通過一種非遺傳重編程產(chǎn)生的，其中含有一種彗星載體組合，包括Oct-4, Sox-2, Klf-4和p53 Anti-sense, EBNA-1。根據(jù)菌落形態(tài)、堿性磷酸酶表達(dá)和SSEA-4表達(dá)驗(yàn)證該細(xì)胞株的多能性。iPS菌落呈現(xiàn)典型的形態(tài)和生長(zhǎng)。證實(shí)無支原體。細(xì)胞系用干冰運(yùn)送。

動(dòng)物種別/Organism  人

組織來源 Tissue and Cell Type iPSC(誘導(dǎo)多能干細(xì)胞)

形態(tài)/Morphology 貼壁生長(zhǎng) 

注意事項(xiàng)：此產(chǎn)品僅供科研使用