Avidin/Biotin Blocking Kit

40 product images

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Micrographs showing T-cells infiltrationMulti-spectral, multicolor Immunofluorescence for T-cells infiltration in lymph nodes samples: dMMR tumor. (200x magnification). Multiplex sequential IF staining on 3-?m sections from FFPE tissue; Tissue sections were treated with an avidin/biotin blocking kit (ab64212) before using a biotin conjugated Foxp3 antibody. Other antibodies were conjugated to fluorochroms. CD4:red, CD8: green, CD4/Foxp3: tile, CD8 blue, EPCAM: yellow

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Representative histological images of detours at the proximal surgical site. Sut: suture, V: vein, ColL: collecting LV, P: panniculus carnosus muscle, A: arterySpecimens for IHC staining of LVs were washed with PBS comprising 0.03% Tween-20 (PBST), incubated with protein blocking solution, endogenous avidin/biotin blocking kit (ab64212), and 0.03% hydrogen peroxide in methanol. The Syrian Hamster anti-podoplanin/gp36 antibody (Anti-Podoplanin antibody [RTD4E10] - BSA and Azide free ab11936) was used at a dilution of 1:600. Subsequently, the specimens were incubated with secondary antibodies linked with biotin (Goat Anti-Syrian Hamster IgG H&L (Biotin) preadsorbed ab7145) followed by streptavidin linked with HRP (Streptavidin (HRP) ab7403).

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  Image from Filliat G., PLoS One 12(7). Fig 6a & b. doi: 10.1371/journal.pone.0181600. Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

  Immunohistochemistry (Frozen sections) - Avidin/Biotin Blocking Kit (ab64212)

  Immunohistochemical analysis staining HTRA1 in mouse bone tissue sections. Tissue sections were dewaxed, rehydrated and treated with Endogenous Avidin/Biotin Blocking Kit (ab64212), 3% H₂O₂ and normal swine serum. Tissue sections were then incubated with a polyclonal anti-HTRA1 antibody for 1 hour at 37°C. After PBS wash, tissue sections are incubated with biotinylated swine anti-rabbit IgG for 45 minutes at 37°C and further incubated for 30 minutes after washing. With Vectastatin. Sections were developed using DAB and counterstained using Harris modified hematoxylin.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of TRBC1 staining in a section of formalin-fixed paraffin-embedded human normal tonsil*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-TCR beta antibody [EPR24928-66] ab323531 at 5ug/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of TRBC1 in a section of formalin-fixed paraffin-embedded human normal liver*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-TCR beta antibody [EPR24928-66] ab323531 at 5ug/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of CYP3A4 in a section of formalin-fixed paraffin-embedded human normal cerebellum*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Cytochrome P450 3A4/CYP3A4 antibody [EPR6202] ab323530 at 0.5ug/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of CYP3A4 staining in a section of formalin-fixed paraffin-embedded human normal liver*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Cytochrome P450 3A4/CYP3A4 antibody [EPR6202] ab323530 at 0.5ug/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of KRT14 staining in a section of formalin-fixed paraffin-embedded human normal skin*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0, epitope retrieval solution 1) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Cytokeratin 14 antibody [SP53] ab323529 at 0.5ug/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of KRT14 in a section of formalin-fixed paraffin-embedded human normal liver*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0, epitope retrieval solution 1) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Cytokeratin 14 antibody [SP53] ab323529 at 0.5ug/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of HLA A staining in a section of formalin-fixed paraffin-embedded human normal small intestine*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-HLA A antibody [EP1395Y] ab322986 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of Tau in a section of formalin-fixed paraffin-embedded human normal cerebral cortex* treated with alkaline phosphatase.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Tau (phospho S396) antibody [E178] ab322984 at 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of Tau staining in a section of formalin-fixed paraffin-embedded human normal cerebral cortex*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Tau (phospho S396) antibody [E178] ab322984 at 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of Langerin in a section of formalin-fixed paraffin-embedded human normal pancreas.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Langerin antibody [EPR15863] ab322985 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of Langerin staining in a section of formalin-fixed paraffin-embedded human normal skin*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Langerin antibody [EPR15863] ab322985 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of Tau staining in a section of formalin-fixed paraffin-embedded mouse normal brain.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Tau (phospho S396) antibody [EPR2731] ab322982 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of Tau in a section of formalin-fixed paraffin-embedded mouse normal brain treated with alkaline phosphatase.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Tau (phospho S396) antibody [EPR2731] ab322982 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of Tau in a section of formalin-fixed paraffin-embedded mouse normal liver.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Tau (phospho S396) antibody [EPR2731] ab322982 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of IgG2 staining in a section of formalin-fixed paraffin-embedded human normal tonsil*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-IgG2 antibody [EPR4418] ab322913 at 0.1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of IgG2 in a section of formalin-fixed paraffin-embedded human normal cerebral cortex*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-IgG2 antibody [EPR4418] ab322913 at 0.1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of IFNG staining in a section of formalin-fixed paraffin-embedded human normal tonsil*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Interferon gamma antibody [EPR21704] ab322914 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of IFNG in a section of formalin-fixed paraffin-embedded human normal skeletal muscle*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Interferon gamma antibody [EPR21704] ab322914 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of DPP4 staining in a section of formalin-fixed paraffin-embedded human normal liver*.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-DPP4 [EPR20819] ab318313 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of DPP4 in a section of formalin-fixed paraffin-embedded human normal brain*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-DPP4 [EPR20819] ab318313 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of Lipocalin-2 in a section of formalin-fixed paraffin-embedded mouse normal brain.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Lipocalin-2 / NGAL [EPR21092] ab318314 at 2µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of Lipocalin-2 staining in a section of formalin-fixed paraffin-embedded mouse spleen.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Lipocalin-2 / NGAL [EPR21092] ab318314 at 2µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of CD5 in a section of formalin-fixed paraffin-embedded human normal brain*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-CD5 [SP19] ab318315 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of CD5 staining in a section of formalin-fixed paraffin-embedded human tonsil*.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-CD5 [SP19] ab318315 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of Cytokeratin 8 staining in a section of formalin-fixed paraffin-embedded human normal stomach*.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0, epitope retrieval solution 1) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Cytokeratin 8 antibody [SP102] - C-terminal ab322309 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of Cytokeratin 8 staining in a section of formalin-fixed paraffin-embedded human breast ductal carcinoma.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0, epitope retrieval solution 1) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Cytokeratin 8 antibody [SP102] - C-terminal ab322309 at 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of Cytokeratin 8 in a section of formalin-fixed paraffin-embedded human normal cerebral cortex*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0, epitope retrieval solution 1) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Cytokeratin 8 antibody [SP102] - C-terminal ab322309 at 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of CD21 in a section of formalin-fixed paraffin-embedded human normal cerebral cortex*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0, epitope retrieval solution 1) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-CD21 antibody [EP3093] ab322303 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of CD21 staining in a section of formalin-fixed paraffin-embedded human normal tonsil*.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0, epitope retrieval solution 1) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-CD21 antibody [EP3093] ab322303 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of CD11c staining in a section of formalin-fixed paraffin-embedded human normal tonsil*.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-CD11c antibody [EP1347Y] - C-terminal ab322302 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of Myeloperoxidase staining in a section of formalin-fixed paraffin-embedded human normal spleen*.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Myeloperoxidase antibody [EPR20257] ab322301 at 0.5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of C3/C3b staining in a section of formalin-fixed paraffin-embedded rat testis.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-C3/C3b antibody [EPR19394] ab322300 at 0.5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of C3/C3b staining in a section of formalin-fixed paraffin-embedded mouse testis.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with a322300 at 1µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of COX2 / Cyclooxygenase 2 staining in a section of formalin-fixed paraffin-embedded human normal small intestine*.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-COX2 / Cyclooxygenase 2 antibody [EPR12012] ab322299 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  Negative staining of CD11b in a section of formalin-fixed paraffin-embedded human normal skeletal muscle*.

  Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-CD11b antibody [EPR1344] ab322298 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of CD11b staining in a section of formalin-fixed paraffin-embedded human normal spleen*.

   Performed on a Leica BOND^TM system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-CD11b antibody [EPR1344] ab322298 at 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.

  *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre.

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  Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Avidin/Biotin Blocking Kit (ab64212)

  IHC image of Uteroglobin staining in a section of formalin-fixed paraffin-embedded mouse lung.

   Performed on a Leica BOND™ system. The section was pre-treated using heat mediated antigen retrieval with EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20mins, before blocking of endogenous biotin using ab64212. The section was then incubated with Biotin Anti-Glutathione Peroxidase 3/GPx-3 antibody [EPR22815-112] ab321782 at 5µg/ml (1/100), for 15 mins at room temperature and detected using an HRP conjugated ABC system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody.

  For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.