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MAPRE1 Knockout Cell Line-293T

MAPRE1 Knockout Cell Line-293T

Cat.No. :  CSC-RT0214

Host Cell:  293T Target Gene:  MAPRE1

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

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Cell Line Information

Cell Culture Information

Safety and Packaging

Cat. No. CSC-RT0214
Description 293T-MAPRE1 (-/-) is a stable cell line with a homozygous knockout of human MAPRE1
Target Gene MAPRE1
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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Background

Publications

Q & A

Customer Reviews

The protein encoded by this gene was first identified by its binding to the APC protein which is often mutated in familial and sporadic forms of colorectal cancer. This protein localizes to microtubules, especially the growing ends, in interphase cells. During mitosis, the protein is associated with the centrosomes and spindle microtubules. The protein also associates with components of the dynactin complex and the intermediate chain of cytoplasmic dynein. Because of these associations, it is thought that this protein is involved in the regulation of microtubule structures and chromosome stability. This gene is a member of the RP/EB family. [provided by RefSeq, Jul 2008]
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
Expedited

MAPRE1 Knockout Cell Line-293T has significantly expedited my research progress, enabling me to unravel the intricate mechanisms of gene function and uncover novel insights into biological processes.

United States

01/27/2022

Bolstered

The outstanding reproducibility of results obtained with MAPRE1 Knockout Cell Line-293T has bolstered the credibility and impact of my scientific findings, reinforcing the robustness of my conclusions.

Germany

07/19/2022

Revolutionized

MAPRE1 Knockout Cell Line-293T has revolutionized my research approach, enabling me to tackle complex research questions and make significant contributions to my field.

United States

11/03/2022

Invaluable

MAPRE1 Knockout Cell Line-293T's profound contribution to advancing our understanding of gene function and its implications in diverse areas of study is invaluable.

United States

02/23/2023

Elevated

By utilizing MAPRE1 Knockout Cell Line-293T, I have elevated the quality and significance of my research, leaving a lasting impact on the scientific community.

France

04/11/2023

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