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Human CDK2 Knockdown Cell Line-HeLa

For research use only. Not intended for any clinical use.

Cat. No. :   CSC-RK0262

Host Cell :   HeLa Validation :   Real-Time RCR

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Cell Line Information

Safety and Packaging

Gene Information

Cat. No. CSC-RK0262
Target Gene CDK2
Abbr HeLa-HuCDK2 Knockdown
Alias CDK2, p33(CDK2)
Host Cell HeLa
Host Cell Species Homo sapiens (Human)
Applications

(1) Studying gene functions

(2) Studying gene interactions and signaling pathways

(3) Target validation and drug discovery

(4) Designing diseases models

Morphology Epithelial
Size >1 × 106 cells / vial
Stability Validated for at least 10 passages
Validation Real-Time RCR
Shipping Dry ice
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
Gene Name CDK2 cyclin-dependent kinase 2 [ Homo sapiens ]
Gene Symbol CDK2
Synonyms p33(CDK2)
Gene Description cyclin-dependent kinase 2
GeneID 1017
Uni ProtID P24941
mRNA Refseq NM_001798.3
Protein Refseq NP_001789.2
Chromosome Location 12q13
Function ATP binding; cyclin binding; cyclin-dependent protein kinase activity; cyclin-dependent protein kinase activity; contributes_to histone kinase activity; metal ion binding; protein binding; protein kinase activity;
Pathway APC/C-mediated degradation of cell cycle proteins, organism-specific biosystem; Activation of ATR in response to replication stress, organism-specific biosystem; Activation of the pre-replicative complex, organism-specific biosystem; B Cell Receptor Signaling Pathway, organism-specific biosystem; BARD1 signaling events, organism-specific biosystem; CDK-mediated phosphorylation and removal of Cdc6, organism-specific biosystem; Cell Cycle, organism-specific biosystem;
MIM 116953
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Background

Q & A

Customer Reviews

The protein encoded by this gene is a member of the cyclin-dependent kinase family of Ser/Thr protein kinases. This protein kinase is highly similar to the gene products of S. cerevisiae cdc28, and S. pombe cdc2, also known as Cdk1 in humans. It is a catalytic subunit of the cyclin-dependent kinase complex, whose activity is restricted to the G1-S phase of the cell cycle, and is essential for the G1/S transition. This protein associates with and is regulated by the regulatory subunits of the complex including cyclin E or A. Cyclin E binds G1 phase Cdk2, which is required for the transition from G1 to S phase while binding with Cyclin A is required to progress through the S phase. Its activity is also regulated by phosphorylation. Two alternatively spliced variants and multiple transcription initiation sites of this gene have been reported. The role of this protein in G1-S transition has been recently questioned as cells lacking Cdk2 are reported to have no problem during this transition.

Customer Q&As
What are the three important functional domains of Cdks?

A: Cdks has three important functional domains. The first functional domain is the binding site of ATP and the active part of the enzyme; the second functional domain is the binding site of the regulatory subunit (Cyclin); the third functional domain is the binding site of P13suc1

How does Cdk drive cells to complete the cell cycle?

A: Various Cdk are activated at specific times during the cell cycle and drive cells to complete the cell cycle by phosphorylating substrates.

How does activated CDK1 keep the cell cycle running?

A: Activated CDK1 phosphorylates target proteins to produce corresponding physiological effects, such as phosphorylation of nucleocapsid proteins leading to nucleocapsid disassembly and loss of nuclear membrane, phosphorylation of H1 leading to condensation of chromosomes, etc. The end result of these effects keeps the cell cycle running.

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