Anti-SOD2/MnSOD (acetyl K122) antibody [NCI-R156-33] - BSA and Azide free (ab240391)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [NCI-R156-33] to SOD2/MnSOD (acetyl K122) - BSA and Azide free
- Suitable for: WB
- Reacts with: Human
Overview
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Product name
Anti-SOD2/MnSOD (acetyl K122) antibody [NCI-R156-33] - BSA and Azide free
See all SOD2/MnSOD primary antibodies -
Description
Rabbit monoclonal [NCI-R156-33] to SOD2/MnSOD (acetyl K122) - BSA and Azide free -
Host species
Rabbit -
Tested Applications & Species
See all applications and species dataApplication Species WB Recombinant fragment -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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General notes
Ab240391 is the carrier-free version of ab214675. This format is designed for use in antibody labeling, including fluorochromes, metal isotopes, oligonucleotides, enzymes.
Our carrier-free formats are supplied in a buffer free of BSA, sodium azide and glycerol for higher conjugation efficiency.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
ab240391 is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm.
Maxpar® is a trademark of Fluidigm Canada Inc.
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
Storage buffer
pH: 7.2
Constituent: PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
NCI-R156-33 -
Isotype
IgG -
Research areas
Images
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This data was developed using ab214675, the same antibody clone in a different buffer formulation.
Flag-SOD2/MnSOD (acetyl K122) was immunoprecipitated from HEK293T cells, transfected with Flag-tagged SOD2/MnSOD (acetyl K122) expression vector and treated with 1µM Trichostatin A (TSA) for 48 h, with anti-Flag antibody.
Western blot was performed from the immunoprecipitate using ab214675 at 1/200 dilution.
Horseradish peroxidase (HRP)-conjugated anti-Rabbit IgG, was used as secondary antibody at 1/10000 dilution.
Lane 1: IP samples washed and incubated with purified SIRT3 protein without NAD+, 10 µg.
Lane 2: IP samples washed and incubated with purified SIRT3 protein with NAD+ for two hours, 10 µg.
Lane 3: IP samples washed and incubated with purified SIRT3 protein without NAD+, then blocked with acetylated peptide (Ac-peptide), 10 µg.
Lane 4: IP samples washed and incubated with purified SIRT3 protein with NAD+ for two hours, then blocked with acetylated peptide (Ac-peptide), 10 µg.
Lane 5: IP samples washed and incubated with purified SIRT3 protein without NAD+, then blocked with non-acetylated control peptide (cont-peptide), 10 µg.
Lane 6: IP samples washed and incubated with purified SIRT3 protein with NAD+ for two hours, then blocked with non-acetylated control peptide (cont-peptide), 10 µg.SIRT3 with NAD+ decreased SOD2/MnSOD acetylation in vitro. The expression profile observed is consistent with what has been described in the literature (PMID: 21172655; 25852572). This data was kindly provided by Dr. Gius (Northwestern University), and has been published in PMID: 21172655.
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