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Gene Editing Services

Ubigene has modified over 5000 genes from more than 100 cell lines with our exclusive innovation CRISPR-U™ technology. At the same time, we already provide customers with high quality gene-editing tools for cell or animal research worldwide.

Stable Cell Lines

Knockout Cell Lines

Knockdown Cell Lines

Overexpression Cell Lines

Knockin Cell Lines

Point Mutation Cell Line

Cloning Services

Knockout Plasmid

Point Mutation Plasmid

Knockin Plasmid

Overexpression Plasmid

Knockdown Plasmid

Virus Packaging

Lentivirus Packaging

Adenovirus Packaging

Adeno-associated Virus Packaging

Microbe

Knockout E.coli

Knockout Salmonella

Cell Assay

Cell Proliferation

Cell Migration and Invasion

Cell Cycle

Cell Apoptosis

Detection of Marker Protein Expression

Cytokine Secretion and Enzyme Activity Test

Cytotoxicity Test

EZ-editor™
Gene-editing Series Products

With 12 years of experience, Ubigene has exclusively innovated and developed 6 product lines, fullfilling all kinds of needs from researchers. Experiment process simplified, efficiency improved, achieving our aim of 'Make genome editing easier'!

Red Cotton™ gRNA Plasmid Bank

Regular Plasmid

Lentiviral Plasmid

EZ-editor™ Culture Medium

Transfection Culture Medium

Cell Monoclonal Culture Medium

Knockout-cell-lysate

KO cell lysates (clone)

KO cell lysates (pool)

EZ-editor™ Cell Line

KO Cell Lines

Wild-type Cell Lines

Cas9 Stable Cell Lines

Luciferase Stable Cell Lines

EGFP Stable Cell Lines

EZ-editor™ Kits

Monoclone Validation Kit (extraction free)

EZ-editor™ Gene Knockout kit

Lentiviral Packaging Kit

Mycoplasma Treatment kit

Lentivirus

Red Cotton Gene knockout Project

Ubigene exclusive KO Cell Line Bank, over 5000 KO cell lines, covering thousands of genes from 8 popular signaling pathways and nearly 100 diseases.

Red Cotton CRISPR Gene Editing Designer

Gene Editing Cell Designer

Gene Editing Microbe Designer

Gene Editing Tool Kit

Red Cotton Gene knockout Project

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New CRISPR tool has the potential to correct almost all disease-causing DNA glitches, scientists repo

New CRISPR tool has the potential to correct almost all disease-causing DNA glitches, scientists report A new form of the genome-editing tool CRISPR-Cas9 appears to significantly expand the range of diseases that could be treated with the technology, by enabling scientists to prec…
2019-12-23
With its CRISPR revolution, China becomes a world leader in genome editing

With its CRISPR revolution, China becomes a world leader in genome editing For many people, CRISPR plus China equals the biophysicist He Jiankui, who infamously used the genome editor last year to alter the DNA of two human embryos that would become twin girls. Before his announce…
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Gene editing enables researchers to correct mutation in muscle stem cells in DMD model

Duchenne muscular dystrophy (DMD) is a rare but devastating genetic disorder that causes muscle loss and physical impairments. Researchers have shown in a mouse study that the powerful gene editing technique known as CRISPR may provide the means for lifelong correction of the gene…
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Researchers Launch First Study of In Vivo CRISPR Therapy in Humans

A trial is recruiting patients to test the gene-editing technology’s ability to treat an inherited form of blindness caused by a mutation in the CEP290 gene.
2019-12-20
Gene-editing technique scientists hope will cure cancer and all inherited disease found to have dange

Gene-editing technique scientists hope will cure cancer and all inherited disease found to have dangerous flaw It has been hailed as a cure for cancer and all forms of inherited disease. But scientists have now discovered that a system for editing the genes of living creatures can…
2019-12-19
High-tech method for uniquely targeted gene therapy developed

Neuroscientists have developed new technology that engineers the shell of a virus to deliver gene therapy to the exact cell type in the body that needs to be treated. The researchers believe that the new technology can be likened to dramatically accelerating evolution from million…
2019-12-19
New CRISPR genome editing system offers a wide range of versatility in human cells

A team has developed a new CRISPR genome-editing approach by combining two of the most important proteins in molecular biology -- CRISPR-Cas9 and a reverse transcriptase -- into a single machine.
2019-12-19
A Brief Guide to the Current CRISPR Landscape

Hundreds of CRISPR patents have been granted around the world, and the number of applications continues to grow at a rapid pace.
2019-09-20
Genes that Are Harmless on Their Own Cause Disease When Combined

A case study of a family demonstrates that different genetic mutations from the two parents cause severe heart disease symptoms in the children.
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