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Anti-BrdU antibody - Proliferation Marker (ab1893)

Overview

  • Product nameAnti-BrdU antibody - Proliferation MarkerSee all BrdU primary antibodies ...
  • Description
    Sheep polyclonal to BrdU - Proliferation Marker
  • Tested applicationsIHC-FrFl, IHC-P, IHC-Fr, IP, ICC/IF, ELISA, IHC-FoFr more details
  • Immunogen

    Bromodeoxyuridine coupled to keyhole limpet hemocyanin (KLH).

Properties

Applications

Our Abpromise guarantee covers the use of ab1893 in the following tested applications.

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

Application Notes
IHC-FrFl IHC-FrFl: Use at an assay dependent concentration.
IHC-P IHC-P: Use a concentration of 10 µg/ml.
IHC-Fr IHC-Fr: Use a concentration of 10 µg/ml.
IP IP: Use a concentration of 25 - 100 µg/ml.
ICC/IF ICC/IF: Use at an assay dependent dilution. PubMed: 21118958
ELISA ELISA: Use at an assay dependent dilution.
IHC-FoFr IHC-FoFr: Use at an assay dependent dilution. PubMed: 19332057

Target

  • RelevanceThe immunocytochemical detection of bromodeoxyuridine (BrdU) incorporated into DNA is a powerful tool to study the cytokinetics of normal and neoplastic cells. In vitro or in vivo labeling of tumor cells with the thymidine analogue BrdU and the subsequent detection of incorporated BrdU with specific anti-BrdU monoclonal antibodies is an accurate and comprehensive method to quantitate the degree of DNA-synthesis. BrdU is incorporated into the newly synthezised DNA of S-phase cells may provide an estimate for the fraction of cells in S-phase. Also dynamic proliferative information such as the S-phase transit rate and the potential doubling time can be obtained, by means of bivariate BrdU/DNA flow cytometric analysis.
  • Cellular localizationNuclear
  • Alternative names
      Bromodeoxyuridine antibodyBUdr antibody

Anti-BrdU antibody - Proliferation Marker images

  • ab1893 used in IP.
  • ab1893 at a 1/50 dilution staining rat brain tissue sections by IHC-P. The incubation time with the primary antibody was overnight at 4°C. This image shows double-staining by polyclonal sheep BrdU (labeled with Cy3 - red) and nestin 401v (labeled with Alexa Fluor® 488 - green). The detection of proliferative (BrdU-positive) astrocytes (some of them express also nestin, which demonstrates that they are reactive and of lower differentiation compared with later stages of reactive astrocytes) within the rat striatum 6 days after striatal neurotoxic lesion (by quolinic acid).

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  • ab1893 Immunofluorescence data

    Tissue culture cells were labelled prior to transplantation and then identified in in vivo tissue using ab1893 sheep polyclonal BrdU antibody (10ug/ml incubated overnight at room temperature) with a TRITC conjugated secondary antibody.

References for Anti-BrdU antibody - Proliferation Marker (ab1893)

This product has been referenced in:
  • Lyons L  et al. Fluoxetine counteracts the cognitive and cellular effects of 5-fluorouracil in the rat hippocampus by a mechanism of prevention rather than recovery. PLoS One 7:e30010 (2012). IHC-Fr . Read more (PubMed: 22272269) »
  • Lee DA  et al. Tanycytes of the hypothalamic median eminence form a diet-responsive neurogenic niche. Nat Neurosci 15:700-2 (2012). Read more (PubMed: 22446882) »

See all 26 Publications for this product

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Application Immunocytochemistry/ Immunofluorescence
Sample Human Cell (colon cancer)
Specification colon cancer
Fixative Paraformaldehyde
Permeabilization Yes - 0.5% Triton-X100
Blocking step Serum as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
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Submitted Jun 07 2012

Application Immunocytochemistry/ Immunofluorescence
Sample Mouse Cell (Paraformaldehyde fixed mouse brain sections)
Specification Paraformaldehyde fixed mouse brain sections
Fixative No
Permeabilization Yes - Triton X-100
Blocking step Serum as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: RT°C
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Submitted Apr 19 2012

Application Immunohistochemistry - Free Floating
Sample Rat Tissue sections (Brain section)
Specification Brain section
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Submitted Nov 17 2011

Application Immunocytochemistry/ Immunofluorescence
Sample Human Cell (Mammary epithelial MCF10A)
Specification Mammary epithelial MCF10A
Fixative 3% paraformaldehyde then 100% methanol
Permeabilization Yes - 2M HCL (30mins RT) for DNA denaturation
Blocking step BSA as blocking agent for 15 minute(s) · Concentration: 2% · Temperature: RT°C
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Submitted Apr 15 2011

Application Immunohistochemistry (Frozen sections)
Sample Mouse Tissue sections (Brain)
Specification Brain
Fixative Paraformaldehyde
Permeabilization No
Blocking step BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
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Submitted Jul 23 2009

Application Immunohistochemistry (Frozen sections)
Sample Mouse Tissue sections (brain)
Specification brain
Fixative Paraformaldehyde
Permeabilization No
Blocking step 2%Blockace/0.05% Triton X-100/PBS as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 2% · Temperature: 25°C
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Submitted Apr 07 2009

Application Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Sample Mouse Tissue sections (Brain: dentate gyrus of Hippocampus)
Specification Brain: dentate gyrus of Hippocampus
Fixative Formaldehyde
Antigen retrieval step Heat mediated - Buffer/Enzyme Used: Modified Citric acid pH6
Permeabilization No
Blocking step BSA as blocking agent for 10 minute(s) · Concentration: 1% · Temperature: rt°C
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Submitted May 30 2008

Application Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Sample Rat Tissue sections (brain (coronal sections of both hemispheres); 6 um)
Specification brain (coronal sections of both hemispheres); 6 um
Fixative Formaldehyde
Antigen retrieval step Heat mediated
Blocking step Serum as blocking agent for 20 minute(s) · Concentration: 1:20
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Submitted Oct 09 2006

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