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Anti-pan Cadherin antibody - Plasma Membrane Marker (ab6529)

Overview

  • Product nameAnti-pan Cadherin antibody - Plasma Membrane MarkerSee all pan Cadherin primary antibodies ...
  • Description
    Rabbit polyclonal to pan Cadherin - Plasma Membrane Marker
  • SpecificityRecognises all cadherin members. Rabbit Anti-Pan Cadherin shows specific reactivity with a distinct 135 kD band on chicken or rabbit heart extract blots using indirect immunoblotting.
  • Tested applicationsIHC-P, WB, ICC/IF, Electron Microscopy, IHC-Fr more details
  • Species reactivity
    Reacts with: Mouse, Rat, Chicken, Cow, Dog, Human, Xenopus laevis, Zebrafish
    Predicted to work with: Rabbit, Bird, Fish, Amphibians
  • Immunogen

    Synthetic peptide: DYDYLNDWGPRFKKLADMYGGGDD conjugated to KLH by a Glutaraldehyde linker, corresponding to C terminal amino acids 889-912 of Chicken pan Cadherin.

  • General notesImmunohistochemistry This antibody has not been tested on frozen sections but has been tested on both cultured cells and formalin-fixed, paraffin-embedded, protease digested sections so chances are it will work on frozen sections. It has also been tested on heart sections and MDBK cells. This antibody should work on bovine samples although we have not tested it specifically.


    This product is useful for the detection of members of the cadherin family or genetically engineered proteins containing the C-terminal cadherin tail, and for demonstration of adherens type cell-cell junctions regardless of their cadherin type.

Properties

Applications

Our Abpromise guarantee covers the use of ab6529 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-P IHC-P: 1/1000. Perform enzymatic antigen retrieval before commencing with IHC staining protocol.
WB WB: 1/200. On chicken and rabbit heart extract this antibody detects a single band at 135 kD.
ICC/IF ICC/IF: 1/100. Fix cells with 2-4% paraformaldehyde for 10 minutes at room temperature, followed by 10-minute incubation with 0.2% Triton X-100 (see Gellersen et al 2007 and Kaur et al 2006).
Electron Microscopy EM: Use at an assay dependent dilution.
IHC-Fr IHC-Fr: Use at an assay dependent dilution. Fix with ice cold ethanol.

Target

  • Alternative names
      Cadherin antibody CDH3 antibody CDHP antibody
      7B4 antigen antibodyCadherin-1 antibodyCadherin-2 antibodyCadherin-3 antibodyCadherin-4 antibodyCadherin-5 antibodyCAM 120/80 antibodyCD144 antibodyCD324 antibodyCD325 antibodyCdh4 antibodyCDH5 antibodyCDHE antibodyCDHN antibodyE-cadherin antibodyEpithelial cadherin antibodyN-cadherin antibodyNCAD antibodyNeural cadherin antibodyP-cadherin antibodyPlacental cadherin antibodyUVO antibodyUvomorulin antibodyVascular endothelial cadherin antibody
    see all

Anti-pan Cadherin antibody - Plasma Membrane Marker images

  • Immunofluorescent imaging of human cells (U2OS) with ab6529 confirms the specificity of this antibody.  Pan cadherin antibody recognises predominantly membranous signal with some fainter cytoplasmic staining corresponding to soluble cadherin. No nuclear staining is seen. 

    IF was performed with a standard paraformaldehyde technique (fixed in PBS buffered PFH 4% for 5 minutes, permeabilised with 0.5% triton-PBS for 5 minutes, blocked with 5% milk / 0.2% tween for one hour.  Primary antibody used at 1/100 in 5% milk / 0.2% TWEEN for one hour, secondary antibody for 30 minutes.  All blocking and incubation steps carried out at 37 degrees C. Nuclei were stained with Hoechst stain.

  • ab6529 staining pan Cadherin in human bone marrow cells by Immunocytochemistry/ Immunofluorescence. The cells were formaldehyde fixed and blocked in 2% BSA for 30 minutes at 20°C. The primary antibody was diluted, 1/200 and incubated with sample for 9 hour at 4°C. An Alexa Fluor® 488 conjugated goat polyclonal to rabbit IgG, diluted 1/200 was used as secondary.

  • This image is courtesy of an anonymous Abreview

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  • ab6529 staining pan Cadherin in rat kidney tissue sections by Immunohistochemistry (frozen sections). Tissue was fixed with acetone and then blocked with 2% BSA for 2 hours at 25°C followed by incubation with the primary antibody, at a 1/200 dilution, for 9 hours at 4°C. The secondary antibody used was a goat anti-rabbit IgG conjugated to Alexa Fluor® 488 (green) used at a 1/500 dilution.

    See Abreview

  • ab6529 staining pan Cadherin in murine liver cells by Immunocytochemistry/ Immunofluorescence. The cells were fixed in formaldehyde, permeabilised in 0.4% Triton X-100 and then blocked using 10% serum for 1 hour at 25°C. Samples were then incubated with primary antibody at 1/200 for 17 hours at 4°C. The secondary antibody used was a goat anti-rabbit IgG conjugated to Alexa Fluor® 594 (red) used at a 1/1000 dilution. The other secondary antibody used was an Alexa Fluor® 488 (green) goat anti-mouse IgG for detection of a specific cytosolic protein.

    See Abreview

References for Anti-pan Cadherin antibody - Plasma Membrane Marker (ab6529)

This product has been referenced in:
  • Mondini A  et al. Hypertension-linked mutation of a-adducin increases CFTR surface expression and activity in HEK and cultured rat distal convoluted tubule cells. PLoS One 7:e52014 (2012). WB ; Rat . Read more (PubMed: 23284854) »
  • Cvrljevic AN  et al. Activation of Src induces mitochondrial localisation of de2-7EGFR (EGFRvIII) in glioma cells: implications for glucose metabolism. J Cell Sci 124:2938-50 (2011). Read more (PubMed: 21878501) »

See all 11 Publications for this product

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Application Immunocytochemistry/ Immunofluorescence
Sample Mouse Cell (Liver (20 um section))
Specification Liver (20 um section)
Fixative Paraformaldehyde
Permeabilization Yes - 0.5% Triton X-100
Blocking step BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 4% · Temperature: 23°C
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Submitted Jan 18 2013

Application Immunocytochemistry/ Immunofluorescence
Sample Human Cell (HepG2)
Specification HepG2
Fixative Paraformaldehyde
Permeabilization No
Blocking step BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 10% · Temperature: 20°C
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Submitted Oct 29 2012

Application Immunocytochemistry/ Immunofluorescence
Sample Mouse Cell (liver)
Specification liver
Fixative Formaldehyde
Permeabilization Yes - 0.4% Triton X-100
Blocking step Serum as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 10% · Temperature: 25°C
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Submitted Jan 26 2011

Application Immunohistochemistry (Frozen sections)
Sample Rat Tissue sections (Kidney)
Specification Kidney
Fixative Acetone
Permeabilization No
Blocking step BSA as blocking agent for 2 hour(s) and 0 minute(s) · Concentration: 2% · Temperature: 25°C
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Submitted Sep 24 2010

Application Immunocytochemistry/ Immunofluorescence
Sample Human Cell (H1299)
Specification H1299
Fixative Paraformaldehyde
Permeabilization Yes - 0.1% Triton X100
Blocking step Serum as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 10% · Temperature: 25°C
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Submitted Aug 11 2010

Application Western blot
Sample Mouse Tissue lysate - whole (brain)
Loading amount 100 µg
Specification brain
Gel Running Conditions Reduced Denaturing
Blocking step Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
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Submitted Jun 02 2010

Application Immunocytochemistry/ Immunofluorescence
Sample Human Cell (293 FT cell line)
Specification 293 FT cell line
Fixative Formaldehyde
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 Jan 21 2010

Application Immunohistochemistry (Frozen sections)
Sample Mouse Tissue sections (Smooth muscle)
Specification Smooth muscle
Fixative Acetone
Permeabilization No
Blocking step BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 4°C
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Submitted Jan 04 2010

Application Immunocytochemistry/ Immunofluorescence
Sample Mouse Cell (bone marrow cell)
Specification bone marrow cell
Fixative Formaldehyde
Permeabilization No
Blocking step BSA as blocking agent for 30 minute(s) · Concentration: 2% · Temperature: 20°C
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Submitted Nov 24 2009

Application Western blot
Sample Mouse Cell lysate - whole cell (c2c12 cells)
Loading amount 30 µg
Specification c2c12 cells
Gel Running Conditions Reduced Denaturing
Blocking step Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 20°C
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Submitted Dec 10 2008



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