ED EDGENS'S SERVICESGENS'S SERVICES EDGENS'S SERVICES

KO Cell Line

  • PBRM1 knockout cell line (A549)
    Cat.No.: EDJ0001-K01
    Gene: PBRM1
    Gene ID: 55193
    Size: 1×10⁶cells
    Cell Form: Adherent
    Price: $1500.00
  • PKM1 knockout cell line (A549)
    Cat.No.: EDJ0002-K02
    Gene: PKM1
    Gene ID: 5315
    Size: 1×10⁶cells
    Cell Form: Adherent
    Price: $1500.00
  • S100A9 knockout cell line (A549)
    Cat.No.: EDJ0003-K03
    Gene: S100A9
    Gene ID: 6280
    Size: 1×10⁶cells
    Cell Form: Adherent
    Price: $1500.00
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Wild Type Cell Line

  • 293T (Human Embryonic Kidney Cell Line)
    Cat.No.: EDC2024001-W01
    Passage Ratio: 1/5,2days
    Price: $980.00
     
  • MPC-5 (Mouse renal podocytes)
    Cat.No.: EDC2024002-W02
    Passage Ratio: 1/4,2days
    Price: $1200.00
     
  • Mac-T (Bovine Breast Epithelial Cell Line)
    Cat.No.: EDC2024003-W03
    Passage Ratio: 1/5, 2days
    Price: $1600.00
     
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ABOUT ED ABOUT EDGENS'SGENS'S ABOUT EDGENS'S

EDITGENE is rooted in independent technology development and upholds the business philosophy of "Innovation · Sharing." We focus on developing and optimizing CRISPR/Cas-based genome editing technologies. Currently, we have established four core technology platforms: Editx™, Bingo™, HES™, and FASST, providing cell gene editing and CRISPR detection CRO services to research institutions and pharmaceutical companies worldwide.

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Years of experience in gene editing

Enable widespreaduse of gene editing
Enable widespreaduse of gene editing

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Client satisfaction has been achieved by EDITGENE

Expand and enhance gene editing applications
Expand and enhance gene editing applications

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Cell lines have been successfully edited genes

Reduce the cost ofgene edit-ing
Reduce the cost ofgene edit-ing

ED EDGENS'S TEAMGENS'S TEAM EDGENS'S TEAM

COOPERATIVE PARTNERS COOPERATIVE PARTNERS

赛默飞
BioTrader,Inc
SATT NORD
University of California, San Francisco
Memorial Sloan Kettering Cancer Center
Cleveland clinic
Jnvena
Texas A&M University School of Dentistry
EVERGREEN
派真生物
RBM
IRBM S.p.A.
Max Planck Institute for Multidisciplinary Sciences
Queen’s University
Sibylla Biotech SpA
Universidade-de-Santiago-de-Compostela
Uppsala universitet
Utah University
Technion-Israel Institute of Technology
Max Planck Institute for Multidisciplinary Sciences

ED EDGENS'S TRUE POWER IN ACTIONGENS'S TRUE POWER IN ACTION EDGENS'S TRUE POWER IN ACTION

WENS FOODSTUFF GROUP CO.. LTD, China
Dr. Zeng

WENS FOODSTUFF GROUP CO.. LTD, China

WENS FOODSTUFF GROUP CO.. LTD, China WENS FOODSTUFF GROUP CO.. LTD, China WENS FOODSTUFF GROUP CO.. LTD, China WENS FOODSTUFF GROUP CO.. LTD, China WENS FOODSTUFF GROUP CO.. LTD, China

The CRISPR detection results of EDITGENE were good. Isothermal amplification plus CRISPR, which is relatively simple,fast and convenient. We will perform futher evaluation for EDITGENE's swine fever testing kit.


Products & Services: CRISPER Detection
SHANGHAI JIAO TONG UNIVERSITY, China
Dr. Yin

SHANGHAI JIAO TONG UNIVERSITY, China

SHANGHAI JIAO TONG UNIVERSITY, China SHANGHAI JIAO TONG UNIVERSITY, China SHANGHAI JIAO TONG UNIVERSITY, China SHANGHAI JIAO TONG UNIVERSITY, China SHANGHAI JIAO TONG UNIVERSITY, China

EDITGENE's CAS enzymes work quite good. I have tried other CAS enzymes on the market before, but EDITGENE's is better. The cutting efficiency detected by EDITGENE's CAS enzyme was higher.


Products & Services: Cell Line Engineering
FOSHAN UNIVERSITY, China
Dr. Liu

FOSHAN UNIVERSITY, China

FOSHAN UNIVERSITY, China FOSHAN UNIVERSITY, China FOSHAN UNIVERSITY, China FOSHAN UNIVERSITY, China FOSHAN UNIVERSITY, China

We ordered overexpression and gene knockout cell lines twice, and all projects were completed quick and with good results. We will continue to order cell line projects with EDITGENE in future.


Products & Services: Cell Line Engineering
HUARUIBANGYAN, China
Dr. Ge

HUARUIBANGYAN, China

HUARUIBANGYAN, China HUARUIBANGYAN, China HUARUIBANGYAN, China HUARUIBANGYAN, China HUARUIBANGYAN, China

EDITGENE provides CRISPR gene edited cells to us. There are other companies that specialize in gene editing, but EDITGENE's R&D and successful rate is better. The quality control and project management are professional. End users are satisfied with projects results.


Products & Services: CRISPR Screening

BUSINESS MAP BUSINESS MAP

Callaboration Case

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Callaboration Case
Cooperative Partner

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Cooperative Partner
Coverage Area

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COLLABORATIVE LITERATURE COLLABORATIVE  LITERATURE

Number of article
Influencing of factor
Numbers of user
Selected Articles Periodical IF Using The Product Corperatvie Partner Link
PAIT effect: Padlock activator inhibits the trans-cleavage activity of CRISPR/Cas12a
Biosensors and Bioelectronics
10.7
LbCas12a
Generation of recombinant antibodies by mammalian expression system for detecting S-metolachlor in
Journal of Hazardous Materials
12.2
Bioactive polysaccharides from Vigna umbellata and its characterization
Biosensors and Bioelectronics
10.7
HCT116 and RAW264.7 Cell Line
Deep whole-genome analysis of 494 hepatocellular carcinomas
nature
50.5
PPP1R12B, KCNJ12, FGA point mutation hepg2 cell line
Electrical stimulation of piezoelectric BaTiO3 coated Ti6Al4V scaffolds promotes anti-inflammatory p
Biomaterials
12.8
RAW264.7 cell line
Optimization of CRISPR/Cas12a detection assay and its application in the detection of Echinococcus g
Veterinary Parasitology
2
LbCas12a
Rapid and Simple Detection of Burkholderia gladioli in Food Matrices Using RPA-CRISPR/Cas12a Method
Foods
4.7
LbCas12a
A Rapid RPA-CRISPR/Cas12a Detection Method for Adulteration of Goat Milk Powder
Foods
4.7
LbCas12a
Targeted Macrophage CRISPR-Cas13 mRNA Editing in Immunotherapy for Tendon Injury
Advanced Science
15.1
LWaCas13a
PAIT effect: Padlock activator inhibits the trans-cleavage activity of CRISPR/Cas12a
Biosensors and Bioelectronics
10.7
LbCas12a
Dumbbell probe initiated multi-rolling circle amplification assisted CRISPR/Cas12a for highly sensit
Biosensors and Bioelectronics
10.7
A super convenient and specific CRISPR/Cas12a diagnostic platform for toxigenic Burkholderia gladiol
Food Control
5.6
ATM depletion induces proteasomal degradation of FANCD2 and sensitizes neuroblastoma cells to PARP i
Induction of Pluripotent Stem Cells from Mouse Embryonic and Adult Fibroblast Cultures by Defined Fa
iPSC-derived lung and lung cancer organoid model to evaluate cisplatin encapsulated autologous iPSC-
Macrophages derived from human induced pluripotent stem cells (iPSCs) serve as a high-fidelity cellu
CLASH enables large-scale parallel knock-in for cell engineering
Modulation of cell cycle increases CRISPR-mediated homology-directed DNA repair
Vasorin (VASN) overexpression promotes pulmonary metastasis and resistance to adjuvant chemotherapy
The alteration of LBX1 expression is associated with changes in parameters related to energy metabol
High Expression of SRSF10 Promotes Colorectal Cancer Progression by Aberrant Alternative Splicing of
ATM depletion induces proteasomal degradation of FANCD2 and sensitizes neuroblastoma cells to PARP i
α1,6-Fucosyltransferase contributes to cell migration and proliferation as well as to cancer stemn
Droplets for Gene Editing Using CRISPR-Cas9 and Clonal Selection Improvement Using Hydrogels
Prime editing functionally corrects cystic fibrosis-causing CFTR mutations in human organoids and ai
The lnc-CTSLP8 upregulates CTSL1 as a competitive endogenous RNA and promotes ovarian cancer metasta
CRISPR/Cas9-mediated knockin of IRES-tdTomato at Ins2 locus reveals no RFP-positive cells in mouse i
Exploring the role of CBLB in acute myocardial infarction: transcriptomic, microbiomic, and metabolo
SENP1-Mediated deSUMOylation Regulates the Tumor Remodeling of Glioma Stem Cells Under Hypoxic Stres
Generation of Human Isogenic Induced Pluripotent Stem Cell Lines with CRISPR Prime Editing
EDGENE

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