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Anti-ATM Antibody (aa1980-2338) LS-C42686


Wt. Vol. Conc. Price
- 100 µl - $370
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)

Most Popular ATM Antibodies

Anti-ATM Antibody (aa980-1512, clone 3E8) IHC-plus™ LS-B1684
Mouse Monoclonal [clone 3E8] (IgG1) to Human ATM
IHC - Paraffin, Western blot, Immunoprecipitation
Immunohistochemistry Image

100% Guaranteed 100% Guaranteed
Rabbit Polyclonal (IgG) to Human ATM
Human, Monkey, Mouse, Hamster
IHC - Paraffin, IHC - Frozen, Western blot, Immunoprecipitation


Human ATM
Human, Monkey, Mouse, Hamster (tested or 100% immunogen sequence identity)
IgG Polyclonal


  • IHC - Paraffin (1:50)
  • IHC - Frozen
  • Western blot (1:500 - 1:1000)
  • Immunoprecipitation

Specificity and Use

ATM antibody was raised against recombinant human ATM fragment (amino acids 1980-2338). ( AA 1980-2338 ).
Recognizes the human ATM protein, a 350kD polypeptide that is the product of the ATM gene. The ATM gene is defective in Ataxia telangiectasia. ATM protein is expressed within the nucleus of all normal cells and is thought to be important in detection of DNA damage.
Immunohistology: This product does require antigen retrieval using heat treatment prior to staining of paraffin sections. We recommend the use of antigen unmasking fluid for this purpose. A two hour incubation with LS-C42686 is recommended.


Serum, 0.09% sodium azide.
For research use only.

About ATM

Q13315 NM_000051 NP_000042.3

ATM Antibody, A-T mutated Antibody, ATA Antibody, ATC Antibody, ATD Antibody, ATE Antibody, AT mutated Antibody, Ataxia telangiectasia Antibody, ATDC Antibody, Serine-protein kinase ATM Antibody, AT1 Antibody, Ataxia telangiectasia mutated Antibody, TEL1 Antibody, TELO1 Antibody

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. Recognizes the substrate consensus sequence [ST]-Q. Phosphorylates 'Ser-139' of histone variant H2AX/H2AFX at double strand breaks (DSBs), thereby regulating DNA damage response mechanism.

Requested From: United States
Date Requested: 10/24/2016

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