News
Current position:Technical Service > Cell Line Development
Cell Line Development
Introduction

In transient transfection, the probability of integrating foreign genes into the genome is very low. The majority of the foreign genes remain in free plasmid form, and as the cells are passaged, the plasmid is gradually lost, leading to dilution of gene copies and preventing sustained expression of the foreign gene. Transfection is typically performed using reagents, and the expression is transient.


When foreign DNA is cloned into a lentiviral vector with a resistance marker and packaged into a virus, the lentivirus can infect target cells. After successful infection, the lentiviral genome integrates into the host cell's chromosome. The resistance marker in the vector allows for selection; cells that have been successfully infected will survive in the culture medium, while uninfected cells will not. Under the selective pressure of the resistance marker, stable cell lines that express the target protein or silence specific genes can be successfully generated.


With years of experience in cell culture and viral packaging, Genomeditech offers a cell line construction service. The service involves infecting target cells with lentivirus carrying foreign genes, and through screening, stable cell lines expressing the target gene can be obtained, which are ideal for gene function studies.


Genomeditech Cell Line Construction Platform

Overexpression Cell Lines

    • 1.1 Mixed Clonal Cell Lines

    • 1.2 Monoclonal Cell Lines

sh Knockdown Cell Lines

    • 2.1 shRNA Custom Cell Lines

    • 2.2 shRNA Cell Line Set

Gene Editing Cell Lines

    • 3.1 Knockout Cell Lines / Conditional Knockout

    • 3.2 Knock-in Cell Lines

    • 3.3 Gene Transcription Activation / Inhibition Cell Lines

    • 3.4 Point Mutation Cell Lines

    • 3.5 Methylated / Demethylated Cell Lines

Reporter Gene Cell Lines

    • 4.1 LUC Reporter Cell Lines


特点

稳定表达细胞株主要应用于以下研究中:

(1)需要长期在目的细胞中研究基因功能。通过构建稳定株,可以大大降低频繁转染或者病毒包装的成本,也方便长期的实验研究;

(2)部分蛋白半衰期及长,瞬时RNA只能干扰表达,无法去除已经表达的目的蛋白,通过构建稳定株可以实验更好的基因干扰效果;

(3)瞬转会引入不可预期的拷贝数表达(往往瞬时表达较高),导致因为人为因素造成实验结果的不精确,构建稳定株可以帮助筛选到拷贝数适量的细胞进行实验研究;

(4)稳转株可以用于诱导表达系统的实验,用于控制基因的时空表达;

(5)需要用目的细胞构建动物模型的实验,往往需要构建成稳定株。

优势

(1)吉满生物专注提供病毒包装服务十余年,稳定细胞系构建服务经验丰富!

(2)吉满生物构建的稳定细胞系种子优良,性状稳定,活力无损!

(3)ISO9001认证的质量体系,严格的病毒纯化工艺!

(4)上万篇SCI期刊引用,包括Cell、Science、Nature等顶级期刊!

(5)完善的客户服务体系,技术支持、项目跟进、售后服务获得客户一致好评,确保您订购无忧!

Current position:Technical Service > Cell Line Development
classify
Cell Line Development
Introduction

In transient transfection, the probability of integrating foreign genes into the genome is very low. The majority of the foreign genes remain in free plasmid form, and as the cells are passaged, the plasmid is gradually lost, leading to dilution of gene copies and preventing sustained expression of the foreign gene. Transfection is typically performed using reagents, and the expression is transient.


When foreign DNA is cloned into a lentiviral vector with a resistance marker and packaged into a virus, the lentivirus can infect target cells. After successful infection, the lentiviral genome integrates into the host cell's chromosome. The resistance marker in the vector allows for selection; cells that have been successfully infected will survive in the culture medium, while uninfected cells will not. Under the selective pressure of the resistance marker, stable cell lines that express the target protein or silence specific genes can be successfully generated.


With years of experience in cell culture and viral packaging, Genomeditech offers a cell line construction service. The service involves infecting target cells with lentivirus carrying foreign genes, and through screening, stable cell lines expressing the target gene can be obtained, which are ideal for gene function studies.


Genomeditech Cell Line Construction Platform

Overexpression Cell Lines

    • 1.1 Mixed Clonal Cell Lines

    • 1.2 Monoclonal Cell Lines

sh Knockdown Cell Lines

    • 2.1 shRNA Custom Cell Lines

    • 2.2 shRNA Cell Line Set

Gene Editing Cell Lines

    • 3.1 Knockout Cell Lines / Conditional Knockout

    • 3.2 Knock-in Cell Lines

    • 3.3 Gene Transcription Activation / Inhibition Cell Lines

    • 3.4 Point Mutation Cell Lines

    • 3.5 Methylated / Demethylated Cell Lines

Reporter Gene Cell Lines

    • 4.1 LUC Reporter Cell Lines


特点

稳定表达细胞株主要应用于以下研究中:

(1)需要长期在目的细胞中研究基因功能。通过构建稳定株,可以大大降低频繁转染或者病毒包装的成本,也方便长期的实验研究;

(2)部分蛋白半衰期及长,瞬时RNA只能干扰表达,无法去除已经表达的目的蛋白,通过构建稳定株可以实验更好的基因干扰效果;

(3)瞬转会引入不可预期的拷贝数表达(往往瞬时表达较高),导致因为人为因素造成实验结果的不精确,构建稳定株可以帮助筛选到拷贝数适量的细胞进行实验研究;

(4)稳转株可以用于诱导表达系统的实验,用于控制基因的时空表达;

(5)需要用目的细胞构建动物模型的实验,往往需要构建成稳定株。

优势

(1)吉满生物专注提供病毒包装服务十余年,稳定细胞系构建服务经验丰富!

(2)吉满生物构建的稳定细胞系种子优良,性状稳定,活力无损!

(3)ISO9001认证的质量体系,严格的病毒纯化工艺!

(4)上万篇SCI期刊引用,包括Cell、Science、Nature等顶级期刊!

(5)完善的客户服务体系,技术支持、项目跟进、售后服务获得客户一致好评,确保您订购无忧!

Message consultation
reset
submit
Service
Message
Message consultation
reset
submit