Human Catalase Antibody

Catalog # Availability Size / Price Qty
MAB3398
MAB3398-SP
Detection of Human Catalase by Western Blot.
4 Images
Product Details
Citations (3)
FAQs
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Human Catalase Antibody Summary

Species Reactivity
Human
Specificity
Detects human Catalase in direct ELISAs and Western blots. In direct ELISAs, no cross-reactivity with recombinant mouse Catalase or recombinant human Serpin C1 is observed.
Source
Monoclonal Mouse IgG1 Clone # 724810
Purification
Protein A or G purified from hybridoma culture supernatant
Immunogen
E. coli-derived recombinant human Catalase
Met1-Leu527
Accession # P04040
Formulation
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
Label
Unconjugated

Applications

Recommended Concentration
Sample
Western Blot
0.5 µg/mL
See below
Simple Western
5 µg/mL
See below
Immunocytochemistry
3-25 µg/mL
See below
Knockout Validated
Catalase is specifically detected in HeLa human cervical epithelial carcinoma parental cell line but is not detectable in Catalase knockout HeLa cell line.
 

Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.

Scientific Data

Western Blot Detection of Human Catalase antibody by Western Blot. View Larger

Detection of Human Catalase by Western Blot. Western blot shows lysates of Jurkat human acute T cell leukemia cell line and Raji human Burkitt's lymphoma cell line. PVDF membrane was probed with 0.5 µg/mL of Mouse Anti-Human Catalase Monoclonal Antibody (Catalog # MAB3398) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # HAF018). A specific band was detected for Catalase at approximately 64 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.

Simple Western Detection of Human Catalase antibody by Simple Western<sup>TM</sup>. View Larger

Detection of Human Catalase by Simple WesternTM. Simple Western lane view shows lysates of Jurkat human acute T cell leukemia cell line, loaded at 0.5 mg/mL. A specific band was detected for Catalase at approximately 61 kDa (as indicated) using 5 µg/mL of Mouse Anti-Human Catalase Monoclonal Antibody (Catalog # MAB3398). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.

Immunocytochemistry Catalase antibody in HL-60 Human Cell Line by Immunocytochemistry (ICC). View Larger

Catalase in HL‑60 Human Cell Line. Catalase was detected in immersion fixed HL-60 human acute promyelocytic leukemia cell line using Mouse Anti-Human Catalase Monoclonal Antibody (Catalog # MAB3398) at 3 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog # NL007) and counterstained with DAPI (blue). Specific staining was localized to peroxisomes. View our protocol for Fluorescent ICC Staining of Non-adherent Cells.

Knockout Validated Western Blot Shows Human Catalase Antibody Specificity by Using Knockout Cell Line. View Larger

Western Blot Shows Human Catalase Specificity by Using Knockout Cell Line. Western blot shows lysates of HeLa human cervical epithelial carcinoma parental cell line and Catalase knockout HeLa cell line (KO). PVDF membrane was probed with 0.5 µg/mL of Mouse Anti-Human Catalase Monoclonal Antibody (Catalog # MAB3398) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # HAF018). A specific band was detected for Catalase at approximately 64 kDa (as indicated) in the parental HeLa cell line, but is not detectable in knockout HeLa cell line. GAPDH (Catalog # MAB5718) is shown as a loading control. This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.

Reconstitution Calculator

Reconstitution Calculator

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Preparation and Storage

Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS.
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Shipping
Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.
Stability & Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 6 months, -20 to -70 °C under sterile conditions after reconstitution.

Background: Catalase

Cells have evolved complex mechanisms to maintain redox balance and defend against oxidative stress. Catalase is a tetrameric enzyme comprised of four 60 kDa subunits. Catalase is typically localized in the peroxisome where it functions as an antioxidant, protecting cells from damage due to oxidative stress. Catalase converts reactive oxygen species, such as H2O2, into water and O2. Human Catalase shares 89% homology to mouse and rat Catalase. The cells redox environment can serve as an important signaling switch or trigger to initiate a number of cellular processes, including gene expression, differentiation, proliferation and apoptosis.

Entrez Gene IDs
847 (Human); 12359 (Mouse); 24248 (Rat)
Alternate Names
Cas1; CAT; Catalase; Cs-1; EC 1.11.1.6; MGC138422; MGC138424

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Citations for Human Catalase Antibody

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

3 Citations: Showing 1 - 3
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  1. Nox4 mediates skeletal muscle metabolic responses to exercise
    Authors: KS Specht, S Kant, AK Addington, RP McMillan, MW Hulver, H Learnard, M Campbell, SR Donnelly, AD Caliz, Y Pei, MM Reif, JM Bond, A DeMarco, B Craige, JF Keaney, SM Craige
    Molecular Metabolism, 2021-01-02;45(0):101160.
    Species: Mouse
    Sample Types: Tissue Homogenates
    Applications: Western Blot
  2. Rejuvenation of mesenchymal stem cells by extracellular vesicles inhibits the elevation of reactive oxygen species
    Authors: Vuong Cat Khanh, Toshiharu Yamashita, Kinuko Ohneda, Chiho Tokunaga, Hideyuki Kato, Motoo Osaka et al.
    Scientific Reports
  3. BNIP3L/NIX regulates both mitophagy and pexophagy
    Authors: Wilhelm LP, Zapata-MuNoz J, Villarejo-Zori B et al.
    The EMBO journal

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