Premade Stable Cell Line

Empowering Discovery with Reporter Stable Cell Line

Cellomics Technology, LLC  has developed the world’s largest collections of genetically engineered stable cell lines to accelerate innovation in academic researches and biotechnology and pharmaceutical R&D. Each of our high-performance cell lines is developed through an evolutionary optimization process — a multi-stage workflow that includes rigorous testing, issue-driven modification, and iterative enhancement — to meet the most demanding research applications. This process takes several months and ensures that the final products deliver:

  • Pure, uniform cell populations
  • Optimized and stable gene expression levels
  • Preserved cellular characteristics
  • Precise, application-ready functional responses
 

The Cellomics premade stable cell line series includes a variety of models tailored for diverse research needs—such as GFP/RFP-labeled cancer cells for in vivo xenograft experiment for animal imaging that can monitor tumor cells growth and metastasis in real-time, CRE-expressing stable cells for gene editing application development, and signaling pathway reporter cell lines for studying the roles of signal transduction pathway in cell behavior.

Cellomics Technology, LLC reporter cell lines includes about more than seven thousands different reporter cell lines, the application of these reporter stable cell lines cover most of common study topics.  Stay tuned for more exciting additions as we continue expanding our product portfolio to empower your innovative research.

Among the lots of publications using our stable reporter cell lines, below are two examples: 

Example 1: Understanding Cancer Invasion in Human Peritoneum

Koch et al., Cancers (2022) 14, 3760. Pharmacologic Targeting of MMP2/9 Decreases Peritoneal Metastasis Formation of Colorectal Cancer in a Human Ex Vivo Peritoneum Culture Model.


In this study, researchers used the Colo205/GFP stable cell line (Cat# SC-1278) engineered by Cellomics Technology, LLC to explore how colorectal cancer cells invade the peritoneum. The Colo205 cells, expressing strong GFP fluorescence, were seeded on patient-derived peritoneal membranes. After 24 hours, GFP-positive Colo205 cells were isolated directly from the peritoneal layer for gene expression profiling. Using this fluorescence-based selection, scientists successfully captured the early molecular events driving cancer cell invasion, revealed by single-cell next-generation sequencing.

Figure 2 (Cancers 2022, 14, 3760) illustrates this workflow — showing the ex vivo peritoneal culture system, the isolation of GFP-expressing Colo205 cells under fluorescence microscopy, and the subsequent transcriptomic analysis identifying MMP-driven mechanisms of metastasis.

Example 2: Tracking Pancreatic Cancer Progression In Vivo


Bhalerao et al., JCI Insight (2023) 8(19):e161563. ST6GAL1 Sialyltransferase Promotes Acinar-to-Ductal Metaplasia and Pancreatic Cancer Progression.


This study examined the role of ST6GAL1 in pancreatic ductal adenocarcinoma (PDAC) using the Suit2 isogenic series, Suit2, S2-013, and S2-LM7AA, which differ in metastatic potential. Each line was genetically engineered by Cellomics Technology, LLC using a CMV-Firefly Luciferase lentiviral vector (PLV-10003: CMV-Firefly luciferase-PGK-puro) to enable in vivo bioluminescent imaging (BLI). This luciferase expression system allowed scientists to track tumor growth and metastatic spread in real time, providing valuable spatial and temporal data on cancer progression. The BLI approach also revealed metastatic lesions in distant organs — such as liver and lung — that would be difficult to identify by conventional methods. Importantly, tumor growth and metastatic burden measured by BLI were consistent with endpoint tumor size and weight, validating the imaging method’s quantitative accuracy.

Figure 1 (JCI Insight, 2023;8(19):e161563) demonstrates that ST6GAL1 is upregulated in metastatic PDAC cells and promotes both tumor growth and metastasis. Overexpression of ST6GAL1 in Suit2 cells increased tumor burden and liver metastases, while knockdown of ST6GAL1 in S2-013 and S2-LM7AA lines suppressed tumor growth and dissemination — confirming ST6GAL1 as a key driver of pancreatic cancer progression.

 

Driving Scientific Impact

These examples highlight how Cellomics Technology’s engineered stable cell lines empower cutting-edge research on dissecting molecular mechanisms of cancer invasion by enabling real-time tracking of tumor dynamics in vivo.

Stable cell lines are invaluable tools for biomedical research and drug discovery, offering consistent and reproducible models for studying complex biological processes. Cellomics’ premade stable cell lines are generated using our well-established lentiviral platform and selected through antibiotic resistance. Because lentiviruses integrate stably into the host genome after transduction, these cell lines continuously express the target genes across subcultures.

 

All the premade stable cell lines can be searched by either the names of cell line, reporter,  or pathway. In case the cell line name has just two characters such as "EA", please then search for "EA cell". Below please find the available most common cell lines and reporters and pathways covered in our collection: 

 

Cell Line Names

 

  • 5637
  • 22RV1
  • 3T3-L1
  • 4T1
  • 769-P
  • 786-O
  • A172
  • A2058
  • A375
  • A549
  • A673
  • ACHN
  • AGS
  • ATDC
  • BEAS-2B
  • BT-20
  • BT-474
  • BT-549
  • BW5147.3
  • BXPC-3
  • C2C12
  • C6
  • CAL-27
  • Calu-3
  • CCRF-CEM
  • CFPAC-1
  • CHO-K1
  • Colo205
  • Colo-320DM
  • CT26 wt
  • DAOY
  • Daudi
  • DLD-1
  • DU145
  • EA
  • ES-2
  • FaDU
  • GH3
  • H4
  • HAP1
  • HCC827
  • HCT116
  • HCT-15
  • HCT-8
  • HEC-1-A
  • HEK293
  • Hela
  • HEP-3B
  • HepG2
  • HH
  • HL60
  • HOS
  • HPAC
  • HPAF-II
  • HS746T
  • HT1080
  • HT1376
  • HT29
  • IMR-32
  • IMR-90
  • IOMM-LEE
  • ISHIKAWA
  • J82
  • JEKO-1
  • Jurkat
  • K1
  • K562
  • K-562
  • KASUMI-1
  • KG-1
  • KLE
  • LL/2
  • LN-229
  • LOVO
  • LS-174T
  • M1
  • MC3T3-E1
  • MCF7
  • MDA-MB-231
  • MEFS
  • MEWO
  • MG-63
  • Mia Paca-2
  • MINO
  • MM1S
  • MOLT-4
  • MRC-5
  • MS751
  • MSTO-211H
  • MV4-11
  • Nalm-6
  • NAMALWA
  • NCI-H1437
  • NCI-H292
  • NCI-H441
  • NCI-H460
  • NCI-H69
  • NCI-H929
  • NIH3T3
  • NTERA-2
  • OVCAR-3
  • Panc-1
  • PBL-2H3
  • PC-3
  • PLC/PRF/5
  • Raji
  • RAMOS
  • Raw264.7
  • RD
  • REH
  • RENCA
  • RKO
  • RPMI-8226
  • RS4;11
  • RT4
  • SCC-15
  • SCC-25
  • SCC-4
  • SCC-9
  • SIHA
  • SJSA-1
  • SK-N-AS
  • SKOV3
  • SNU-1
  • SNU-16
  • SR
  • SU-DHL-4
  • SU-DHL-6
  • SUP-B15
  • SW1990
  • SW48
  • SW620
  • T24
  • T47D
  • T98G
  • TALL-104
  • TCCSUP
  • TF-1
  • THP-1
  • TT
  • TuTu80
  • U2OS
  • U-87 MG
  • UM-UC3
  • VCAP
  • ZR-75-1
  •  
    Reporter/Pathways/Imaging

     

  • AP1-JNK-firefly luciferase reporter
  • AP1-JNK-GFP reporter
  • AP1-JNK-RFP reporter
  • Calcium Indicator GCaMP6f reporter
  • Calcium Indicator GCaMP6s reporter
  • Calcium Indicator GCaMP7 reporter
  • Calcium Indicator GCaMP8 Reporter
  • cAMP-PKA Pathway CRE GFP Reporter
  • cAMP-PKA Pathway CRE Pathway Firefly Luciferase Reporter
  • cAMP-PKA Pathway CRE RFP Reporter
  • cell cycle S Reporter
  • Cre Recombinase Reporter
  • Cre-GFP Reporter
  • Cre-RFP Reporter
  • firefly luciferase
  • Firefly luciferase-GFP Reporter
  • firefly luciferase-HSV1-tk Reporter
  • FLP Recombinase Reporter
  • Fluc-miRFP670
  • G1 phase YFP-labeled
  • GFP Reporter
  • GFP-Firefly Luciferase Reporter
  • GFP-firefly luciferase-HSV1-tk Reporter
  • Hedgehog Pathway Firefly Luciferase Reporter
  • Hedgehog Pathway GFP reporter
  • Hedgehog Pathway RFP reporter
  • HSV1-tk Reporter
  • HSV1-tk-firefly luciferase Reporter
  • IFNbeta-Firefly Luciferase Reporter
  • IFNbeta-GFP Reporter
  • IFNbeta-RFP Reporter
  • JAK-Stat Pathway Firefly Luciferase Reporter
  • JAK-Stat Pathway GFP Reporter
  • JAK-Stat Pathway RFP Reporter
  • MAPK-ERK ELK1 Pathway Firefly Luciferase Reporter
  • MAPK-ERK Pathway ELK1 GFP Reporter
  • MAPK-ERK Pathway ELK1 RFP Reporter
  • MAPK-ERK Pathway SRE Pathway Firefly Luciferase reporter
  • MAPK-ERK SRE Pathway GFP Reporter
  • MAPK-ERK SRE Pathway RFP Reporter
  • NFAT-Firefly Luciferase Reporter
  • NFAT-GFP Reporter
  • NFAT-RFP Reporter
  • NF-KB Firefly Luciferase Reporter
  • NF-kB-GFP Reporter
  • NF-kB-RFP Reporter
  • Notch Pathway Firefly Luciferase Reporter
  • Notch Pathway GFP Reporter
  • Notch Pathway RFP Reporter
  • Nuclear GFP Reporter
  • Nuclear RFP Reporter
  • PI3K-AKT Pathway Firefly Luciferase Reporter
  • PI3K-AKT Pathway GFP Reporter
  • PI3K-AKT Pathway RFP Reporter
  • RFP Reporter
  • RFP-Firefly Luciferase Reporter
  • RFP-Firefly Luciferase-HSV1-tk Reporter
  • Tet-rtTA Reporter
  • TGFbeta-SMAD-Firefly Luciferase Reporter
  • TGFbeta-SMAD Pathway GFP Reporter
  • TGFbeta-SMAD Pathway RFP Reporter
  • TGF-β Pathway Firefly Luciferase Reporter
  • Wnt-β-Catenin Pathway Firefly Luciferase Reporter
  • Wnt-β-Catenin Pathway GFP Reporter
  • Wnt-β-Catenin Pathway RFP Reporter
  •  

    The above products can also be browsed through the below five categories.

     

     

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