Name: DNA Damage Control Cell Extracts
Price: 165.00 USD
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Product Information

Product Usage Information

Boil for 3 min prior to use. Load 10 µL of phosphorylated and nonphosphorylated DNA Damage Control Cell Extracts per lane.

Storage

Supplied in SDS Sample Buffer: 62.5 mM Tris- HCl (pH 6.8 at 25°C), 2% w/v SDS, 10% glycerol, 50 mM DTT, 0.01% w/v bromophenol blue or phenol red. Store at –20°C, or at –80°C for long-term storage.

Product Description

Nonphosphorylated DNA Damage Control Cell Extracts: Total cell extracts from 293 cells to serve as a negative control. Supplied in SDS Sample Buffer.

Phosphorylated DNA Damage Control Cell Extracts: Total cell extracts from 293 cells, treated with 100 mJ/cm² UV light and a 2 hr recovery, serve as a positive control. Supplied in SDS Sample Buffer.

This control cell extract has been validated using Cell Signaling Technology^® antibodies, as referenced in the figure captions. Please refer to the product webpage or datasheet for specific antibody information.

Background

Ataxia telangiectasia mutated (ATM) and ATM and Rad3-related (ATR) kinases are PI3K-related kinase (PIKK) family members that phosphorylate multiple substrates on serine or threonine residues that are followed by a glutamine in response to DNA damage or replication blocks (1-3). p53 is phosphorylated by ATM, ATR, and DNA-PK at Ser15. This phosphorylation impairs the ability of MDM2 to bind p53, thereby promoting accumulation and activation of p53 in response to DNA damage (4,5). Chk1 and Chk2, downstream protein kinases of ATM/ATR, play an important role in DNA damage checkpoint control, embryonic development, and tumor suppression (6). Chk1 is phosphorylated at Ser280 and Ser296 following DNA damage. The amino-terminal domain of Chk2 contains a series of seven serine or threonine residues, including Thr68, each followed by glutamine (SQ or TQ motif). After DNA damage by ionizing radiation (IR), UV irradiation, or hydroxyurea treatment, Thr68 and other sites in this region become phosphorylated by ATM/ATR (7-9). The breast cancer susceptibility proteins BRCA1 and BRCA2 are frequently mutated in cases of hereditary breast and ovarian cancers and have roles in multiple processes related to DNA damage, repair, cell cycle progression, transcription, ubiquitination, and apoptosis. Numerous DNA-damage-induced phosphorylation sites on BRCA1 have been identified, including serine 1524, and kinases activated in a cell cycle-dependent manner, including Aurora A and CDK2, can also phosphorylate BRCA1. IR, DNA, and radiometric-induced DNA damage also result in rapid phosphorylation of the histone H2A family member H2A.X at Ser139 by ATM (10,11). Within minutes following DNA damage, Ser139-phosphorylated H2A.X localizes to sites of DNA damage at subnuclear foci (12).

Alternate Names

DNA damage; extract; lysate

限制使用

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For Research Use Only. Not for Use in Diagnostic Procedures.

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.

U.S. Patent No. 7,429,487, foreign equivalents, and child patents deriving therefrom.

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DNA Damage Control Cell Extracts #4768