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Human CDK4 Knockout Cell Line-HCT116

Human CDK4 Knockout Cell Line-HCT116

Cat.No. :  CSC-RT2742

Host Cell:  HCT116 Target Gene:  CDK4

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

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Cell Line Information

Cell Culture Information

Safety and Packaging

Cat. No. CSC-RT2742
Description This cell is a stable cell line with a homozygous knockout of human CDK4 using CRISPR/Cas9.
Target Gene CDK4
Host Cell HCT116
Host Cell Species Homo sapiens (Human)
Size Form 1 vial (>10^6 cell/vial)
Shipping Dry ice package
Storage Liquid Nitrogen
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

Applications

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Q & A

Customer Reviews

CDK4 (Cyclin-dependent kinase 4) is an essential protein in humans, encoded by the CDK4 gene. The main function of CDK4 is to participate in the G1-S phase of the cell cycle, acting as a catalytic subunit in a protein kinase complex. The activity of CDK4 is tightly regulated by its binding to D-type cyclins and the CDK inhibitor p16INK4a. More specifically, CDK4 phosphorylates the retinoblastoma protein (Rb), an important step in regulating cell cycle progression. This phosphorylation event dissociates the E2F transcription factor from the Rb/E2F complex and subsequently initiates transcription of E2F target genes responsible for G1 phase progression. In addition to its role in normal cell cycle regulation, CDK4 has important clinical implications, especially in cancer. Mutations in CDK4 and its associated regulatory proteins, including D-type cyclins, p16INK4a, CDKN2A, and Rb, have been implicated in various cancers. A specific mutation, CDK4 (R24C), was initially identified in melanoma patients. This mutation has been extensively studied in animal models, confirming its role as an oncogene. Due to its widespread involvement in tumorigenesis, CDK4 has emerged as a promising target for cancer therapy. Various CDK4 inhibitors are currently in clinical trials to evaluate their efficacy in treating different types of cancer.
Cancer Research: This cell line is useful for studying the role of CDK4 in cancer cell proliferation. By comparing the proliferation rates of CDK4 knockout cells to wild-type HCT116 cells, researchers can better understand how CDK4 promotes tumor growth, potentially identifying new targets for cancer treatment. Drug Development: The CDK4 knockout HCT116 cell line can be used as a model for screening and evaluating CDK4 inhibitors and other therapeutic agents. It provides insight into the efficacy and specificity of potential drugs, allowing researchers to identify compounds that specifically target the CDK4 pathway without affecting other cellular mechanisms. Cell Cycle Regulation Studies: CDK4 plays a critical role in the cell cycle, specifically the transition from G1 to S phase. This knockout cell line is useful for elucidating the molecular mechanisms involved in cell cycle regulation and determining how CDK4 loss affects cell cycle progression. Genomic Studies: This cell line can be used for genetic studies, including studying gene regulation, expression, and the effects of CDK4 loss on the broader genomic landscape. It can be used to study compensatory mechanisms that cells may employ in the absence of CDK4. Signal Transduction Studies: CDK4 is part of several signal transduction pathways. By using CDK4 knockout cell lines, researchers can dissect these pathways and understand how the loss of CDK4 affects various signaling cascades.
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
Invaluable tool

By studying CDK4 knockout cells, we can assess the effect of CDK4 loss on cell behavior, providing valuable insights into its role in cancer development.

United States

08/23/2020

Worked very well

The CDK4 KO cell line has high specificity, so it is easy to detect expression.

United States

01/27/2022

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