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  1. Link

    human-cat-catalase-knockout-hela-cell-pellet-ab278971.pdf

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Tags & Cell Markers Subcellular Markers Organelles Peroxisome
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Human CAT (Catalase) knockout HeLa cell pellet (ab278971)

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Western blot - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
  • Western blot - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
  • Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
  • Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
  • Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)

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Anti-Catalase antibody [EP1929Y] - Peroxisome Marker (ab76024)

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Overview

  • Product name

    Human CAT (Catalase) knockout HeLa cell pellet
    See all Catalase kits
  • Product overview

    Abcam’s knockout cell pellets give you access to native proteins, without the need to culture cells. Our knockout cell pellets are prepared from our single-gene knockout cell lines and provide an additional offering to our cell lysates.

    Cells are snap-frozen to provide high quality pellets that are suitable for extraction with alternative lysis buffers or for preparation of lysates from subcellular fractions. Our knockout cell pellets are suitable for a variety of applications, including PCR, gene expression profiling and DNA library preparation.

  • Parental Cell Line

    HeLa
  • Organism

    Human
  • Mutation description

    Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon1 and 4 bp deletion in exon1 and Insertion of the selection cassette in exon1.
  • Passage number

    <20
  • Knockout validation

    Sanger Sequencing, Western Blot (WB)
  • Notes

    Pellet size: 5 million cells/vial.

    This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.

  • Tested applications

    Suitable for: WBmore details

Properties

  • Storage instructions

    Store at -80°C. Please refer to protocols.
  • Components 1 kit
    Human CAT knockout HeLa cell pellet 1 vial
    Human wild-type HeLa cell pellet 1 vial
  • Research areas

    • Tags & Cell Markers
    • Subcellular Markers
    • Organelles
    • Peroxisome
    • Signal Transduction
    • Protein Trafficking
    • Chaperones
    • Heat Shock Proteins
    • Cardiovascular
    • Heart
    • Cardiac metabolism
    • Cancer
    • Cancer Metabolism
    • Cellular metabolic process
    • Metabolism
    • Pathways and Processes
    • Redox metabolism
    • Antioxidants
  • Cell type

    epithelial
  • Disease

    Adenocarcinoma
  • Gender

    Female
  • STR Analysis

    Amelogenin X D5S818: 11, 12 D13S317: 12, 13.3 D7S820: 8, 12 D16S539: 9, 10 vWA: 16, 18 TH01: 7 TPOX: 8,12 CSF1PO: 9, 10

Target

  • Function

    Occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide. Promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells and normal and transformed fibroblast cells.
  • Involvement in disease

    Defects in CAT are the cause of acatalasia (ACATLAS) [MIM:115500]; also known as acatalasemia. This disease is characterized by absence of catalase activity in red cells and is often associated with ulcerating oral lesions.
  • Sequence similarities

    Belongs to the catalase family.
  • Post-translational
    modifications

    The N-terminus is blocked.
  • Cellular localization

    Peroxisome.
  • Target information above from: UniProt accession P04040 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • Alternative names

    • Cas1
    • CAT
    • CATA_HUMAN
    • Catalase
    • Cs1
    • MGC138422
    • MGC138424
    see all

Associated products

  • KO cell lines

    • Human CAT (Catalase) knockout HeLa cell line (ab265250)
  • KO cell lysates

    • Human CAT (Catalase) knockout HeLa cell lysate (ab256859)
  • Related Products

    • Anti-Catalase antibody [EPR20198] (ab209211)
    • Anti-Catalase antibody [EPR20198] - BSA and Azide free (ab223793)
    • Anti-Catalase antibody [EP1929Y] - BSA and Azide free (ab227116)
    • Anti-Catalase antibody [EP1929Y] - Peroxisome Marker (ab76024)

Applications

The Abpromise guarantee

Our Abpromise guarantee covers the use of ab278971 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB
Use at an assay dependent concentration. Predicted molecular weight: 60 kDa.
Notes
WB
Use at an assay dependent concentration. Predicted molecular weight: 60 kDa.

Images

  • Western blot - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
    Western blot - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)

    Lane 1: Wild-type HeLa cell lysate (20 µg)

    Lane 2: CAT knockout HeLa cell lysate (20 µg)

    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] 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.

  • Western blot - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
    Western blot - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)

    Lane 1: Wild-type HeLa cell lysate (20 µg)

    Lane 2: CAT knockout HeLa cell lysate (20 µg)

    Lanes 1-2: Merged signal (red and green). Green - ab76024 observed at 60 kDa. Red - loading control ab8245 observed at 37 kDa.

    ab76024 Anti-Catalase antibody [EP1929Y] - 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. ab76024 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 10000 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.

  • Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
    Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)

    Allele-1: 4 bp deletion in exon1

     

  • Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
    Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)

    Allele-2: 1 bp deletion in exon1

     

  • Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)
    Sanger Sequencing - Human CAT (Catalase) knockout HeLa cell pellet (ab278971)

    Allele-3: Insertion of the selection cassette in exon1

     

Protocols

To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

Click here to view the general protocols

Datasheets and documents

  • Datasheet download

    Download

References (0)

Publishing research using ab278971? Please let us know so that we can cite the reference in this datasheet.

ab278971 has not yet been referenced specifically in any publications.

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