Acetyl-Lysine Antibody Mouse Monoclonal (7B5A1)

Acetyl Lysine Mouse Monoclonal Antibody

Mouse / IgG2b


Species Reactivity
All species

Validation Data
Ac-K Antibody White Paper
IF: Ac-K Mitochondria



AAC02, Anti-acetyl lysine antibody is a pan-acetyl lysine mouse monoclonal antibody that is part of the Signal-Seeker™ product line.The Anti-acetyl-lysine antibody recognizes proteins post-translationally modified by acetylation on the epsilon amine groups of lysine residues that occur on 30-50% of all proteins and in particular histones, p53, tubulin and myosin. A proprietary mixture of acetylated proteins was used to produce a highly robust antibody that has been shown to recognize a wide range of acetylated proteins in IP, WB, ChIP and IF applications. This Anti-acetyl-lysine antibody has many advantages when compared to other commercially available antibodies; in particular, it can be used to visualize acetylated mitochondrial proteins by IF.

Validated Applications

Western Blot using Acetyl-Lysine Antibody (AAC02)

 Fig 1: A: Murine tissue extract, 30 μg brain extract. B: 30 μg of Cos-7 cell lysate treated with TSA and nicotinamide (+) or untreated (-).  Strongly enhanced  bands at 55 and 14-16 kDa in TSA-treated lysate correspond to acetylated tubulin and histone proteins, respectively. C: Titration of acetylated BSA. Lanes 1-5 contain 0.5, 0.1, 0.05, 0.01, and 0.005 ng Ac-BSA, lanes 6-7 contain 500 and 1000 ng non-acetylated BSA, respectively.  AAC02 was used at a 1:500 dilution following the recommended western blot protocol.

To see the full Western blot comparison, see the Optimized Protocols or the product datasheet.

Acetyl Lysine Western Blot

Immunoprecipitation using Acetyl-Lysine Antibody

 Fig 2:  Cos-7 cells were either treated (+) or untreated (-) with TSA (1 μM) and nicotinamide (1 mM) for 6 hours.  Cell lysates were prepared in BlastR buffer and filter system and 1 mg of lysate per reaction was used for IP of acetylated proteins.  20 μl of AAC02 was used per IP reaction. Western blots of immunoprecipitated proteins were developed using AAC03-HRP at 1:3000 dilution.

To see the full Immunoprecipitation comparison, see the Optimized Protocols or the product datasheet.

Acetyl Lysine Immunoprecipitation
Immunofluorescence using Acetyl-Lysine Antibody 
 Fig 3: Swiss 3T3 cells, untreated (a and c) or treated (b and d) with TSA (1 μM for 6 h), were stained as described in the datasheet. Acetylated proteins were visualized using a green fluorescent secondary. Actin fibers were visualized using a red Rhodamine Phalloidin and the nucleus was stained with DAPI. The acetylated microtubule network is clearly visible with TSA-treatment, while the green fluorescent nuclear intensity indicate the high abundance of acetylated proteins in the nucleus. In c and d, acetylated BSA (10 mg/ml) was used to  compete for AAC02 binding as an indicator of AAC02 specificity for acetyl-lysine modifications.

To see the full Immunofluorescence protocol, see the Optimized Protocols or the product datasheet.

Acetyl Lysine IF
AAC02 detects mitochondrial acetylation by IF 
Fig 4: Swiss 3T3 cells, either untreated or treated with TSA (1 μM for 6h), were stained as described in the method. (a and d): Mitochondria were visualized with MitoTracker orange (Thermo Fisher). (b and e): Acetylated proteins were visualized in green fluorescence. (c and f): Merged image of mitochondrial and acetylation signals. Actin fibers and nuclei were visualized in purple with Rhodamine Phalloidin and blue with DAPI respectively. Note: AAC02 provides broad, pan acetyl-lysine detection including acetylated mitochondrial , nuclear, and cytoplasmic proteins.


To see the full Immunofluorescence protocol, see the Optimized Protocols or the product datasheet.

Acetyl Lysine ChIP
ChIP using Acetyl-Lysine Antibody
 Fig 5: Utilization of AAC02 for ChIP. Chromatin was prepared from A431 cells, either untreated or treated with TSA (1 μM) and nicotinamide (1 mM) for 6 hours. ChIP was performed as described. mIgG: mouse IgG used for ChIP control; AAC02: anti-acetyl lysine antibody used for ChIP; Input: cell lysate prior to ChIP; H2O: Water used as PCR control. The PCR products obtained with GAPDH primers are 166 bp.  

To see the recommended ChIP protocol, see the Optimized Protocols or the product datasheet

Acetyl Lysine ChIP

Protein Acetylation Background

Acetylation of proteins can occur as a co-translational or post-translational modification  (PTM) (1).  Co-translational acetylation occurs at the N-terminal of approximately 85% of mammalian proteins, it is irreversible and is thought to be important in protein stability, localization and synthesis (1).  Post-translational acetylation occurs on the epsilon amino group of lysine residues as a reversible and highly dynamic PTM that is known to be a key regulator in multiple cellular events, including chromatin structure, transcription,  metabolism,  signal transduction and cytoskeletal regulation (2-3).  To date over 4,000 proteins have been identified as targets for PTM acetylation which is comparable to phosphorylation in cellular prevelance (3).  Antibody AAC01 detects acetyl lysine PTMs. 



1 Bogdan P. and Sherman F. 2002. The diversity of acetylated proteins. Genome Biol. 3 (5): reviews 0006.

2 Lundby A. et al. 2012. Proteomic analysis of lysine acetylation sites in rat tissues reveals organ specificity and cellular patterns. Cell Reports 2:419-431.

3 Sadoul K. et al. 2010. The tale of protein lysine acetylation in the cytoplasm.  J. Biomed. Biotech. 2011:1-15.

4 Golemis EA et. Al, Protein-Protein Interactions, CSHLP, 2005, p67

For more information contact:

Associated Products:

Signal-Seeker™ Acetyl-Lysine Detection Kit (Cat. # BK163)

Signal-Seeker™: BlastR™ Rapid Lysate Prep Kit (Cat. # BLR01)

Signal-Seeker™ Acetylation Affinity Beads (Cat.# AAC04-beads)

For product Datasheets, MSDSs, and COAs please click on the PDF links below.


Sample Size Datasheet (Cat. AAC02-s):  

Certificate of Analysis:  available upon request


AuthorTitleJournalYearArticle Link
Horita, Henrick et al.Utilizing optimized tools to investigate PTM crosstalk: Identifying potential PTM crosstalk of acetylated mitochondrial proteinsProteomes2018ISSN 2227-7382

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