Anti-Catalase antibody [EPR20198] - Peroxisome Marker
- KO Validated
- RabMAb
- Recombinant
- Lab Essentials
- 20ul selling size
- What is this?
5
(3 Reviews)
|
(37 Publications)
Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) is a rabbit monoclonal antibody detecting Catalase in Western Blot, Flow Cytometry (Intra), ICC/IF. Suitable for Human, Mouse, Rat.
- KO validated for confirmed specificity
- Biophysical QC for unrivalled batch-batch consistency
- Over 20 publications
View Alternative Names
Catalase, CAT
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed C2C12 (Mouse myoblast cell line) cells labeling Catalase with ab209211 at 1/60 dilution (red) compared withRabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730; black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody; blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized C2C12 (Mouse myoblast cell line) cells labeling Catalase with ab209211 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on C2C12 cell line. The nuclear counterstain is DAPI (blue).
Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) at 1/200 dilution (red).
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) at 1/1000 dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
ImmunoFluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized NIH/3T3 (Mouse embryonic fibroblast cell line) cells labeling Catalase with ab209211 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on NIH/3T3 cell line. The nuclear counterstain is DAPI (blue).
Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) at 1/200 dilution (red).
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) at 1/1000 dilution.
- WB
AbReview76889****
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
4-20% tris-glycin gel
All lanes:
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) at 1/2000 dilution
All lanes:
SHSY5Y cell lysate at 40 µg
Secondary
All lanes:
Anti-rabbit IgG, HRP-linked Antibody #7074 at 1/10000 dilution
false
Exposure time: 12min
This image is courtesy of an anonymous Abreview
- WB
Lab
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
Lanes 1-2 : Merged signal (red and green). Green - ab209211 observed at 60 kDa. Red - loading control ab8245 observed at 37 kDa.
ab209211 Anti-Catalase antibody [EPR20198] - Peroxisome Marker was shown to specifically react with Catalase in wild-type HeLa cells. Loss of signal was observed when knockout cell line ab265250 (knockout cell lysate ab256859) was used. Wild-type and Catalase knockout samples were subjected to SDS-PAGE. ab209211 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 2000 and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) at 1/2000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
CAT knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human CAT (Catalase) knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-cat-catalase-knockout-hela-cell-line-ab265250'>ab265250</a>)
Predicted band size: 60 kDa
Observed band size: 60 kDa
false
- WB
Supplier Data
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
Blocking/Dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) at 1/2000 dilution
Lane 1:
Human fetal brain lysate at 10 µg
Lane 2:
Human fetal heart lysate at 10 µg
Lane 3:
Human fetal kidney lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG Peroxidase Conjugate, specific to the non-reduced form of IgG at 1/10000 dilution
Predicted band size: 60 kDa
Observed band size: 60 kDa
false
Exposure time: 1min
- WB
Lab
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
Lanes 1 - 4 : Merged signal (red and green). Green - ab209211 observed at 60 kDa. Red - loading control, ab8245, observed at 37 kDa.
ab209211 was shown to specifically react with CAT in wild-type HAP1 cells. No band was observed when CAT knockout samples were examined. Wild-type and CAT knockout samples were subjected to SDS-PAGE. ab209211 and ab8245 (Mouse anti GAPDH loading control) were incubated overnight at 4°C at 1/2000 dilution and 1/10,000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) ab216776 secondary antibodies at 1/10,000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) at 1/2000 dilution
Lane 1:
Wild-type HAP1 whole cell lysate at 20 µg
Lane 2:
CAT knockout HAP1 whole cell lysate at 20 µg
Lane 3:
Hek293 whole cell lysate at 20 µg
Lane 4:
HepG2 whole cell lysate at 20 µg
Predicted band size: 60 kDa
false
- WB
Supplier Data
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
Blocking/Dilution buffer : 5% NFDM/TBST.
Exposure time : Lane 1 : 1 second; Lane 2/3/6 : 3 seconds; Lane 4/5 : 30 seconds.
All lanes:
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) at 1/2000 dilution
Lane 1:
C6 (Rat glial tumor cell line) whole cell lysate at 10 µg
Lane 2:
PC-12 (Rat adrenal gland pheochromocytoma cell line) whole cell lysate at 10 µg
Lane 3:
NIH/3T3 (Mouse embryonic fibroblast cell line) whole cell lysate at 10 µg
Lane 4:
HepG2 (Human liver hepatocellular carcinoma cell line) whole cell lysate at 10 µg
Lane 5:
HEK-293 (Human epithelial cell line from embryonic kidney) whole cell lysate at 10 µg
Lane 6:
C2C12 (Mouse myoblast cell line) whole cell lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 60 kDa
Observed band size: 60 kDa
false
- WB
AbReview76890****
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
4-20% tris-glycin gel
All lanes:
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) at 1/2000 dilution
All lanes:
Balb/C mice brain tissue lysate at 40 µg
Secondary
All lanes:
Anti-rabbit IgG, HRP-linked Antibody #7074 at 1/10000 dilution
false
Exposure time: 6min
This image is courtesy of an anonymous Abreview
- WB
Supplier Data
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
Blocking/Dilution buffer : 5% NFDM/TBST.
Exposure time : Lane 1-3 : 5 seconds; Lane 4/5 : 1 second; Lane 6 : 3 seconds.
All lanes:
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) at 1/2000 dilution
Lane 1:
Mouse brain lysate at 10 µg
Lane 2:
Mouse heart lysate at 10 µg
Lane 3:
Mouse spleen lysate at 10 µg
Lane 4:
Mouse kidney lysate at 10 µg
Lane 5:
Rat heart lysate at 10 µg
Lane 6:
Rat brain lysate at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 60 kDa
Observed band size: 60 kDa
false
- WB
CiteAb
Western blot - Anti-Catalase antibody [EPR20198] - Peroxisome Marker (AB209211)
Catalase western blot using anti-Catalase antibody [EPR20198] - Peroxisome Marker ab209211. Publication image and figure legend from Peng, K. T., Tsai, M. H., et al., 2018, PLoS One, PubMed 30125327.
ab209211 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab209211 please see the product overview.
Expression of various ROS-related proteins, pro-inflammatory factors, and an osteoclast differentiation factor RANKL in tissue samples of all treated groups at 24 weeks after surgery.(A) Representative Western blot analysis of transferrin, catalase, SOD1, SOD2, SOD3, GPx1, GPx2, TTR, NF-κB, IL-1β and RANKL in different groups. GAPDH was used as internal control. (B) Densitometric quantification of Western blot analysis for all tested proteins normalized to GAPDH (n = 3 for each group). *, p < 0.05, for results compared to those of the sham group; #, p < 0.05, for results compared to those of the group receiving an artificial knee joint only.
false
Related conjugates and formulations (1)
-
Anti-Catalase antibody [EPR20198] - BSA and Azide free
Reactivity data
Product details
What is this antibody validated in?
Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) is a rabbit recombinant monoclonal antibody and is validated for use in Western Blot (WB), Flow Cytometry (Intra), Flow Cytometry (Flow Cyt), Immunocytochemistry/immunofluorescence (ICC/IF) in Human, Mouse, Rat samples.
What is the molecular weight of Catalase?
Anti-Catalase [EPR20198] - Peroxisome Marker (ab209211) specifically detects a band for Catalase (UniProt: P24270) at a molecular weight of 60kDa.
Trusted by the scientific community
Anti-Catalase [EPR20198] - Peroxisome Marker (ab209211) was first used in a scientific publication in 2016 and has been cited over 20 times in peer-reviewed journals.
Trial sizes available!
Test your antibody or perform pre-screening before committing to a larger quantity. Sold in 10µl. Discover our selection of trial-size antibodies.
Specificity confirmed
The specificity of Anti-Catalase antibody [EPR20198] - Peroxisome Marker (ab209211) has been confirmed by Western blot testing in Catalase Knockout HAP1 cells.
Other related products
We have a range of other formats of antibody clone [EPR20198] also available for your convenience: ab209211, Carrier free - ab223793
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
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 batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Catalase contributes to antioxidant defense by breaking down hydrogen peroxide preventing cellular damage. In peroxisomes it works alongside other peroxisomal enzymes to maintain cell health and metabolic regulation. Catalase does not form a complex but interacts closely with other enzymes like superoxide dismutase which dismutates superoxide radicals into less harmful substances. Increased Catalase activity levels can be measured using Catalase activity kits and activity assays allowing us to learn about peroxisome function.
Pathways
Hydrogen peroxide removal by Catalase is vital in the reactive oxygen species (ROS) metabolic process and plays a part in the cellular response to oxidative stress. Catalase interacts with the glutathione peroxidase pathway safeguarding cells from oxidative stress-related damage. Superoxide dismutase works synergistically with Catalase transforming superoxide anions into hydrogen peroxide before its decomposition by Catalase. These activities highlight the essential role Catalase plays in protecting cells from oxidative stress damage.
Product protocols
- Visit the General protocols
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Target data
Publications (37)
Recent publications for all applications. Explore the full list and refine your search
Cell reports. Medicine 6:102052 PubMed40239632
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Food & function 16:539-553 PubMed39688297
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Antioxidants (Basel, Switzerland) 13: PubMed39594503
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Cellular and molecular biology (Noisy-le-Grand, France) 70:85-91 PubMed38836676
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Chemico-biological interactions 394:110991 PubMed38582340
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Life sciences 342:122541 PubMed38428572
2024
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PloS one 19:e0289248 PubMed38335199
2024
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Neural regeneration research 19:2019-2026 PubMed38227531
2024
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Small (Weinheim an der Bergstrasse, Germany) 20:e2309454 PubMed38098368
2023
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Molecular neurobiology 61:2313-2335 PubMed37874483
2023
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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