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3D4/21-Luc

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3D4/21-Luc
Copy Product Info
Catalog#
YC-C041-Luc-P
Size
1*10^6 Cells/vial (frozen vial)
Culture method
85%RPMI-1640+10%FBS+1%Glutamax+1%SodiumPyruvate+1%NEAA+1%Hepes+2.2g/L Glucose
Price(USD)
$1590
Instruction
-

Overview

Gene reporter systems are widely used in studies of eukaryotic gene expression and cellular physiology, serving as a common approach to improving experimental accuracy and reliability. The luciferase reporter system, which detects luciferase activity using luciferin or firefly aldehyde as substrates, is one of the most extensively applied reporter systems. Owing to its operational simplicity, high sensitivity, and high success rate, it is widely applied in gene expression research.

The 3D4/21-Luciferase cell line developed by Ubigene was generated using the lentivirus method. In addition to enabling stable and high-efficiency expression of the luciferase gene, it offers high specificity, excellent imaging quality, and accurately quantifiable luminescence intensity. This cell line supports a broad range of downstream applications, including promoter activity analysis, mammalian two-hybrid assays, and in vivo animal imaging studies. Its flexibility and quantitative performance make it reliable for gene regulation research, functional validation, and preclinical model development.

Detailed Product Information

3D4/21-Luc
Product name
3D4/21-Luc
Reporter gene
Firefly Luciferase
Catalog number
YC-C041-Luc-P
Resistance gene
Puromycin
Product category
Luciferase Stable Cell Lines
Mycoplasma test
Negative
Species
Pig
Accession
-
Cell morphology
Macrophage-like, adherent
Shipping condition
Frozen vials; dry-ice package
Passage ratio
1:2~1:3
Storage condition
Liquid nitrogen
Culture method
85%RPMI-1640+10%FBS+1%Glutamax+1%SodiumPyruvate+1%NEAA+1%Hepes+2.2g/L Glucose
Intended use
For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use.
Background

The parental porcine monomyeloid cell line, 3D4, was established in December of 1998 following transfection of primary porcine alveolar macrophage cultures with the pSV3neo plasmid. Single cell cloning and selection in G-418 of the 3D4 parental cell line resulted in establishment of 3D4/2 (ATCC CRL-2845), 3D4/21 (ATCC CRL-2843) and 3D4/31 (ATCC CRL-2844).

Product Advantages

Easy to use
Easy to use

Cas9 cell lines in our cell bank can stably express Cas9 protein. Each Cas9 Stable Cell Line is easy to use and enables gene knockout simply by transfecting gRNA, while transfection of gRNA and donor DNA results in gene knock-in or point mutations

High-efficient KO
High-efficient KO

These Cas9 stable cell lines have been used to construct the KO cell lines for various genes, gene KO efficiency 5-10 times improved.

Curated cells
Curated cells

Selected cells, low passages, good cell condition, high activity, applicable for all kinds of gene-editing experiments.

Plasmid Backbone Map

Plasmid Backbone Map

View Picture

Quality Control

1. Bacteria and fungi test
None Detected.
2. Mycoplasma test
Negative.
4. Luciferase stable expression validation
In vivo imaging process
In vivo imaging process
Figure 1. In vivo imaging process of luciferase stable tumor cell line
Luciferase validation process
Luciferase activity was detected using the Dual-Luciferase® Reporter Assay System Kit(Promega, Cat: E1910), and the firefly luciferase reaction intensity was read in the Microplate Reader (BioTek, Synergy LX).
In vivo imaging process
Figure 2. Luciferase activity validation workflow
RT-qPCR Test Results
Sample NameDuplicated well 1Duplicated well 2Duplicated well 3Average valueRatio
3D4/21-Luc----NaN
3D4/21----

Intended use

For research use only. Not intended for human or animal clinical trials, therapeutic or diagnostic use

Unpacking and Storage Instructions

1.
Cell Reception
2.
Unpacking and storage instructions

Handling procedure

1.
Cell Thawing
2.
Cell Passaging
3.
Cell cryopreservation

References

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