14-933-M

ATM, active

• Synonym(s): Ataxia telangiectasia mutated
• UNSPSC Code: 12352200
• eCl@ss: 32160405
• NACRES: NA.32

Properties

• biological source: human
• Quality Level: 100
• mol wt: M_w 352 kDa
• manufacturer/tradename: Upstate^®
• technique(s): activity assay: suitable (kinase)
• NCBI accession no.: NM_000051
• UniProt accession no.: Q13315
• Gene Information: human ... ATM(472)

Description

General description

Research area: CANCER

Product Source: Recombinant, human FLAG-tagged ATM full length, expressed in a mammalian cell line.

The Ataxia telangiectasia mutated protein (ATM) is a serine/threonine protein kinase primarily found in the nuclei of cells and plays a crucial role in cellular processes. It shows similarities with phosphatidylinositol-3′-kinases and possesses inherent protein kinase activity. Located on chromosome 11 (11q22-23), the ATM gene comprises 66 exons and codes for the ATM protein consisting of 3056 amino acids. The ATM protein is made up of various domains and belongs to the phosphatidylinositol 3-kinase-related kinase (PIKK) superfamily. ATM kinase forms inactive homodimers under normal conditions and is activated under stressful conditions like DNA structural changes, oxidative stress, nutrient deprivation, or hypoxia.

Application

ATM protein has been used for in vitro ATM kinase assays to check the radiosensitization induced in pancreatic cells by kinase inhibition.

Biochem/physiol Actions

The Ataxia telangiectasia mutated protein (ATM), belonging to the phosphatidylinositol 3-kinase family, is involved in multiple cellular signaling pathways. It serves as a key regulator of the DNA double-strand break (DSB) repair pathway by sensing these breaks and regulating the physiological responses through tumor protein 53 (TP53), checkpoint kinase 1 (CHK1), and checkpoint kinase 2 (CHK2) pathways. It is also involved in activating proteins like p53 and cdc25C, thus acting as a tumor suppressor. Moreover it serves an important role in mitogenic signal transduction, meiotic recombination, and cell cycle control. However, loss in ATM activity leads to development of ataxia-telangiectasia (AT), a rare autosomal recessive disorder causing neurodegeneration, hypersensitivity to radiation, immune deficiencies, and an increased susceptibility to cancer. Alterations in the ATM gene are frequently observed in various types of cancer, including breast, pancreatic, prostate, and ovarian cancer. Necessary for activation of ABL1 and SAPK. Phosphorylates DYRK2, CHEK2, p53/TP53, FANCD2, NFKBIA, BRCA1, CTIP, nibrin (NBN), TERF1, RAD9 and DCLRE1C. May play a role in vesicle and/or protein transport. May play a role in vesicle and/or protein transport. Could play a role in T-cell development, gonad and neurological function. Plays a role in replication-dependent histone mRNA degradation.

Packaging

Also available in 250μg size as catalog # 14-933M and in bulk as catalog # 14-933-K.

Quality

Routinely evaluated by phosphorylation of recombinant human p53, full length (c-Myc, 6His tagged) as the substrate (Millipore cat # 23-034)

Physical form

Protein in frozen storage buffer

Storage and Stability

6 months at -70°C

Other Notes

For Specific Activity data, refer to the Certificate of Analysis for individual lots of this enzyme.

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.