Data
Human Testis (formalin-fixed, paraffin-embedded) stained with ATM antibody at 5 ug/ml followed by biotinylated anti-mouse IgG secondary antibody, alkaline phosphatase-streptavidin and chromogen.
Detection of human ATM protein using anti-ATM 2C1 monoclonal antibody (3310) by western blot or immunoprecipitation.
Human Kidney (formalin-fixed, paraffin-embedded) stained with ATM antibody at 5 ug/ml followed by biotinylated anti-mouse IgG secondary antibody, alkaline phosphatase-streptavidin and chromogen.![Whole cell extract (30 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with ATM antibody [2C1] (3310) diluted at 1:1000.](https://www.leinco.com/wp-content/uploads/2025/01/qed-bioscience-anti-atm-antibody-3310-4.jpg)
Whole cell extract (30 ug) was separated by 5% SDS-PAGE, and the membrane was blotted with ATM antibody [2C1] (3310) diluted at 1:1000.![HeLa whole cell extract and nuclear extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with ATM antibody [2C1] (3310) diluted at 1:500. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.](https://www.leinco.com/wp-content/uploads/2025/01/qed-bioscience-anti-atm-antibody-3310-5.jpg)
HeLa whole cell extract and nuclear extracts (30 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with ATM antibody [2C1] (3310) diluted at 1:500. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody.![ATM antibody [2C1] detects ATM protein at nucleus by immunohistochemical analysis. Sample: Paraffin-embedded human breast carcinoma. ATM stained by ATM antibody [2C1] (3310) diluted at 1:100. Antigen Retrieval: Citrate buffer, pH 6.0, 15 min](https://www.leinco.com/wp-content/uploads/2025/01/qed-bioscience-anti-atm-antibody-3310-6.jpg)
ATM antibody [2C1] detects ATM protein at nucleus by immunohistochemical analysis.
Sample: Paraffin-embedded human breast carcinoma.
ATM stained by ATM antibody [2C1] (3310) diluted at 1:100.
Antigen Retrieval: Citrate buffer, pH 6.0, 15 min![Untreated (–) and treated (+) 293T whole cell extracts (60 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with ATM antibody [2C1] (3310) diluted at 1:1000. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](https://www.leinco.com/wp-content/uploads/2025/01/qed-bioscience-anti-atm-antibody-3310-7.jpg)
Untreated (–) and treated (+) 293T whole cell extracts (60 ug) were separated by 5% SDS-PAGE, and the membrane was blotted with ATM antibody [2C1] (3310) diluted at 1:1000. The HRP-conjugated anti-mouse IgG antibody was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced. - -
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Antibody DetailsProduct DetailsReactive Species Human ⋅ Monkey ⋅ Mouse ⋅ Rat Host Species Mouse Immunogen GST fusion protein expressed in E. coli corresponding to aa 2577- 3056 of full-length ATM. Product Concentration Lot Specific Formulation PBS, pH 7.4 State of Matter Liquid Product Preparation Purified by Protein G affinity chromatography Storage and Handling This antibody is stable for at least one (1) year at -70°C. Avoid multiple freeze-thaw cycles. Regulatory Status Research Use Only Country of Origin USA Shipping Next Day 2-8°C Applications and Recommended Usage? Quality Tested by Leinco Immunoblotting: use at 1-10 ug/mL.
Immunoprecipitation: use at 1-10 ug/mL. Positive controls: Raji or Akata cells. Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionSpecificity This antibody recognizes full-length ATM, a 370 kD nuclear phosphoprotein, which is involved in the autooal recessive disease ataxia telangiectasia (AT). ATM belongs to a novel family of proteins associated with cell cycle regulation and response to DNA repair. The C-terminal region has extensive homology to the catalytic domains of phosphatidylinositol 3-kinases (PI3 kinases). Its usefulness to monitor altered ATM expression in cancer is under active investigations. Function Serine/threonine protein kinase which activates checkpoint signaling upon double strand breaks (DSBs), apoptosis and genotoxic stresses such as ionizing ultraviolet A light (UVA), thereby acting as a DNA damage sensor. RPubMed:10550055, PubMed:10766245, PubMed:10802669, PubMed:10839545, PubMed:10910365, PubMed:10973490, PubMed:11375976, PubMed:12086603, PubMed:12556884, PubMed:14871926, PubMed:15448695, PubMed:15456891, PubMed:15916964, PubMed:16086026, PubMed:16858402, PubMed:17923702, PubMed:19431188, PubMed:19965871, PubMed:26774286, PubMed:29203878, PubMed:30612738, PubMed:30886146, PubMed:9733514, PubMed:9733515, PubMed:9843217}. NCBI Gene Bank ID UniProt.org Research Area Cancer Research References & CitationsChen, G and EY-HP Lee (1996) J Biol Chem 271: 33693-33697. Technical Protocols FACS ICC IF    Chromatin IP (ChIP) IHC-P Certificate of Analysis |
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Products are for research use only. Not for use in diagnostic or therapeutic procedures.
