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CCNI Knockout Cell Line-293T

CCNI Knockout Cell Line-293T

Cat.No. :  CSC-RT0220

Host Cell:  293T Target Gene:  CCNI

Size:  1x10^6 cells/vial, 1mL Validation:  Sequencing

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Cell Line Information

Cell Culture Information

Safety and Packaging

Cat. No. CSC-RT0220
Description 293T-CCNI (-/-) is a stable cell line with a homozygous knockout of human CCNI
Background The protein encoded by this gene belongs to the highly conserved cyclin family, whose members are characterized by a dramatic periodicity in protein abundance through the cell cycle. Cyclins function as regulators of CDK kinases. Different cyclins exhibit distinct expression and degradation patterns which contribute to the temporal coordination of each mitotic event. This cyclin shows the highest similarity with cyclin G. The transcript of this gene was found to be expressed constantly during cell cycle progression. The function of this cyclin has not yet been determined. [provided by RefSeq, Jul 2008]
Target Gene CCNI
Host Cell 293T
Host Cell Species Homo sapiens (Human)
Revival Rapidly thaw cells in a 37°C water bath. Transfer contents into a tube containing pre-warmed media. Centrifuge cells and seed into a 25 cm2 flask containing pre-warmed media.
Mycoplasma Negative
Format One frozen vial containing millions of cells
Storage Liquid nitrogen
Safety Considerations

The following safety precautions should be observed.

1. Use pipette aids to prevent ingestion and keep aerosols down to a minimum.

2. No eating, drinking or smoking while handling the stable line.

3. Wash hands after handling the stable line and before leaving the lab.

4. Decontaminate work surface with disinfectant or 70% ethanol before and after working with stable cells.

5. All waste should be considered hazardous.

6. Dispose of all liquid waste after each experiment and treat with bleach.

Ship Dry ice
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Q & A

Customer Reviews

Customer Q&As
How is the knockout cell line validated?

A: The knockout cell product is validated by PCR amplification and Sanger Sequencing to confirm the mutation at the genomic level. Please find the detailed mutation info in the datasheet.

Is the product a single clonal cell or mixed cell pool?

A: Single clonal cell.

Can I confirm gene knockout by RT-qPCR?

A: No. This knockout cell product is generated using the CRISPR/Cas9 system to induce small insertions or deletions (indels) resulting in frameshift mutations. Although these frameshift mutations typically disrupt the coding gene, there is a possibility that the non-functional transcript may still be transcribed. Consequently, this could potentially yield misleading results when analyzed by RT-qPCR.

How can I store the cell product?

A: The cell line should be stored in liquid nitrogen for long-term preservation.

Is it possible to get multiple knockout clones for my GOI?

A: For most cases, we often keep at least 2 clones with different frameshift mutations. Please feel free to contact us to check if there are additional available clones.

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Customer Reviews
Grateful

As my research journey unfolds, I am grateful for the opportunities CCNI Knockout Cell Line-293T has provided me, propelling me towards new discoveries and scientific breakthroughs.

United States

10/09/2021

Extends

CCNI Knockout Cell Line-293T's impact extends beyond the laboratory, as it has allowed me to collaborate with researchers from diverse backgrounds, fostering a sense of camaraderie and shared passion for genetics.

United States

01/27/2022

Future research endeavors

Through using CCNI Knockout Cell Line-293T, I have honed my technical skills and gained valuable insights into the fascinating world of gene manipulation, paving the way for future research endeavors.

Germany

07/19/2022

Confident

As I reflect on my scientific achievements, I am confident that CCNI Knockout Cell Line-293T will remain an indispensable tool in my pursuit of knowledge and innovation in the realm of genetics.

United States

11/03/2022

Continues

With immense gratitude, I acknowledge the transformative role of CCNI Knockout Cell Line-293T, as it continues to shape and inspire my path as a dedicated researcher.

United States

02/23/2023

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