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Anti-Catalase antibody - Peroxisome Marker (ab1877)

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Overview

Product name

Anti-Catalase antibody - Peroxisome Marker
See all Catalase products (3) ...

Description

Rabbit polyclonal to Catalase - Peroxisome Marker

Tested applications

IHC-Fr, IHC-P, ICC, WB, IP, ELISA, ICC/IFmore details

Cross reactivity

Reacts with

Mouse, Rat, Sheep, Chicken, Cow, Human

Immunogen

Catalase [Bovine Liver]

Positive control

ICC: MDCK cells, COS-1 cells (see review) IHC-P: rat or mouse liver sections (see review) WB: rat thoracic aorta and vena cava lysate (see review)

General notes

This product has been assayed against 1.0 ug of Catalase [Bovine liver] in a standard ELISA using Peroxidase conjugated Affinity Purified anti-Rabbit IgG [H&L] (Goat) and (ABTS (2,2'-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid]) as a substrate for 30 minutes at room temperature. A working dilution of 1:30,000 to 1:150,000 is suggested for this product.Storage: Aliquot contents and freeze at -20° C or below. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid.

Properties

Form

Liquid

Storage instructions

Please see Notes section

Storage buffer

Preservative: 0.01% Sodium Azide
Constituents: 50% Glycerol, 1% BSA, PBS, 0.15M Sodium Chloride, 0.02M Potassium Phosphate. pH 7.2

Concentration

Concentration information loading...

Purity

Preadsorbed IgG fraction

Purification notes

This product is an IgG fraction antibody purified from monospecific antiserum by a multi-step process which includes delipidation, salt fractionation and ion exchange chromatography followed by extensive dialysis against the buffer stated above. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Rabbit Serum as well as purified and partially purified Catalase [Bovine liver].

Clonality

Polyclonal

Isotype

IgG

  • Immunocytochemistry/ Immunofluorescence - Catalase antibody - Peroxisome Marker (ab1877)Immunocytochemistry/ Immunofluorescence - Catalase antibody - Peroxisome Marker (ab1877) image (enlarge)

  • Western blot - Catalase antibody - Peroxisome Marker (ab1877)Western blot - Catalase antibody - Peroxisome Marker (ab1877) image (enlarge)

  • Western blot - Catalase antibody - Peroxisome Marker (ab1877)Western blot - Catalase antibody - Peroxisome Marker (ab1877) image (enlarge)

Applications

Show applications key

Our Abpromise guarantee covers the use of ab1877 in the following tested applications.

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

Target

Relevance

Catalase is the classical marker for peroxisomes and is the most abundant protein within peroxisomes.

Alternative names

  • Cas 1 antibody
  • CAT antibody
  • Cs1 antibody
  • MGC138422 antibody
  • MGC138424 antibody
see all

Anti-Catalase antibody - Peroxisome Marker images:

  Immunocytochemistry/ Immunofluorescence - Catalase antibody - Peroxisome Marker (ab1877)

Immunocytochemistry/ Immunofluorescence - Catalase antibody - Peroxisome Marker (ab1877)

ab1877 at a dilution of 1/200 staining Hydrogen peroxide treated HeLa cells (1mM, 1hr) by immunocytochemistry. The antibody was incubated with the cells for 2 hours and then detected using a Cy5 conjugated anti-rabbit antibody.

This image is courtesy of an Abreview submitted by Jinhee Kim on 30 January 2006.

See Abreview

  Western blot - Catalase antibody - Peroxisome Marker (ab1877)

Western blot - Catalase antibody - Peroxisome Marker (ab1877)

All lanes : Anti-Catalase antibody - Peroxisome Marker (ab1877) at 1/5000 dilution

Lane 1 : 3ug liver 1 (Homogenate)
Lane 2 : 3ug liver 1 (PNS)
Lane 3 : 3ug liver 1 (Float 1)
Lane 4 : 3ug liver 1 (Float 2)
Lane 5 : 3ug liver 1(Interface - enriched fraction)
Lane 6 : 3ug liver 2 (Homogenate)
Lane 7 : 3ug liver 2 (PNS)
Lane 8 : 3ug liver 2 (Float 1)
Lane 9 : 3ug liver 2 (Float 2)
Lane 10 : 3ug liver 2(Interface - enriched fraction)

Secondary
HRP conjugated goat polyclonal antibody
developed using the ECL technique

Predicted band size : 59 kDa
Observed band size : 65 kDa (why is the actual band size different from the predicted?)
Additional bands at : <25 kDa (possible degradation product).

Exposure time : 5 seconds

This image is courtesy of an anonymous Abreview

See Abreview

  Western blot - Catalase antibody - Peroxisome Marker (ab1877)

Western blot - Catalase antibody - Peroxisome Marker (ab1877)


developed using the ECL technique

Performed under reducing conditions.

Predicted band size : 59 kDa
Observed band size : 64 kDa (why is the actual band size different from the predicted?)


Exposure time : 3 minutes

ab1877 at 1/500 staining human placenta (whole tissue lysate) by WB (20ug/lane). An HRP donkey anti-rabbit antibody was used as the secondary. The image shows 6 samples each from normal and preeclamptic placenta.

This image is courtesy of an Abreview submitted by Dr Rose Webster

See Abreview

  Immunoprecipitation - Anti-Catalase antibody - Peroxisome Marker (ab1877)

Immunoprecipitation - Anti-Catalase antibody - Peroxisome Marker (ab1877)

Catalase was immunoprecipitated using 0.5mg Hela whole cell extract, 5µg of Rabbit polyclonal to Catalase (ab1877) and 50µl of protein G magnetic beads (lane 1). The antibody was incubated with the Protein G beads for 10min under agitation. No antibody was added to the control (lane 2). Hela whole cell extract diluted in RIPA buffer was added to each sample and incubated for 10min under agitation. Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab1877. Secodary: Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697).
Bands: 60kDa: Catalase

References for Anti-Catalase antibody - Peroxisome Marker (ab1877)

This product has been referenced in:

  • Berg RK  et al. Genomic HIV RNA induces innate immune responses through RIG-I-dependent sensing of secondary-structured RNA. PLoS One 7:e29291 (2012). ICC/IF; Human.Read more (PubMed: 22235281) »
  • Panov AV  et al. Metabolic and functional differences between brain and spinal cord mitochondria underlie different predisposition to pathology. Am J Physiol Regul Integr Comp Physiol 300:R844-54 (2011).Read more (PubMed: 21248309) »

See all 38 publications for this product

Publishing research using ab1877? Please let us know so that we can cite the reference in this datasheet

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"