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P-cadherin Rabbit mAb (A25549)

Datasheet

Tested applications:WBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibitionReactivity:Human

ABclonal:Western blot - P-cadherin Rabbit mAb (A25549)

Western blot analysis of various lysates using P-cadherin Rabbit mAb (A25549) at 1:3000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Negative control (NC): SH-SY5Y.
Exposure time: 30s.

ABclonal:Immunofluorescence - P-cadherin Rabbit mAb (A25549)

Confocal immunofluorescence analysis of A-431 cells using P-cadherin Rabbit mAb (A25549, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.

ABclonal:Immunofluorescence - P-cadherin Rabbit mAb (A25549)

Confocal imaging of paraffin-embedded Human breast cancer tissue using P-cadherin Rabbit mAb (A25549, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval with 0.01 M citrate buffer (pH 6.0) prior to IF staining. Objective: 40x.

ABclonal:Flow CytoMetry - P-cadherin Rabbit mAb (A25549)

Flow cytometry: 1X10^6 MCF7 cells (Low Expression, left) and A-431 cells (right) were surface-stained with P-cadherin Rabbit mAb (A25549, 2 μg/mL, orange line) or ABflo® 647 Rabbit IgG isotype control (A22070, 5 μl/Test, blue line), followed by Alexa Fluor® 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).

ABclonal:Flow CytoMetry - P-cadherin Rabbit mAb (A25549)

Flow cytometry: 1X10^6 A-431 cells were surface-stained with ABflo® 647 Rabbit IgG isotype control (A22070, 5 μl/Test, left) or P-cadherin Rabbit mAb (A25549, 2 μg/mL, right).

Overview

Product nameP-cadherin Rabbit mAb
Catalog No.A25549
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC66488
This gene encodes a classical cadherin of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature glycoprotein. This calcium-dependent cell-cell adhesion protein is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. This gene is located in a gene cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. In addition, aberrant expression of this protein is observed in cervical adenocarcinomas. Mutations in this gene are associated with hypotrichosis with juvenile macular dystrophy and ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome (EEMS).
ImmunogenRecombinant fusion protein containing a sequence corresponding to amino acids 108-654 of human P-cadherin (NP_001784.2).
SequenceDWVVAPISVPENGKGPFPQRLNQLKSNKDRDTKIFYSITGPGADSPPEGVFAVEKETGWLLLNKPLDREEIAKYELFGHAVSENGASVEDPMNISIIVTDQNDHKPKFTQDTFRGSVLEGVLPGTSVMQVTATDEDDAIYTYNGVVAYSIHSQEPKDPHDLMFTIHRSTGTISVISSGLDREKVPEYTLTIQATDMDGDGSTTTAVAVVEILDANDNAPMFDPQKYEAHVPENAVGHEVQRLTVTDLDAPNSPAWRATYLIMGGDDGDHFTITTHPESNQGILTTRKGLDFEAKNQHTLYVEVTNEAPFVLKLPTSTATIVVHVEDVNEAPVFVPPSKVVEVQEGIPTGEPVCVYTAEDPDKENQKISYRILRDPAGWLAMDPDSGQVTAVGTLDREDEQFVRNNIYEVMVLAMDNGSPPTTGTGTLLLTLIDVNDHGPVPEPRQITICNQSPVRQVLNITDKDLSPHTSPFQAQLTDDSDIYWTAEVNEEGDTVVLSLKKFLKQDTYDVHLSLSDHGNKEQLTVIRATVCDCHGHVETCPGPWKGG
Gene ID
Swiss Prot
SynonymsCDHP; HJMD; PCAD
Calculated MW87kDa/91kDa
Observed MW120kDa
ReactivityHuman
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:3000 - 1:12000
  • IF/ICC 1:200 - 1:800
  • FC 1:500 - 1:1000
  • ELISA Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Storage bufferStore at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.05% proclin300, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    Immunofluorescence    Flow Cytometry    
Positive samplesHaCaT
Cellular locationCell membrane, Single-pass type I membrane protein.

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ABclonal:Western blot - P-cadherin Rabbit mAb (A25549)}

Western blot - P-cadherin Rabbit mAb (A25549)

Western blot analysis of various lysates using P-cadherin Rabbit mAb (A25549) at 1:3000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Negative control (NC): SH-SY5Y.
Exposure time: 30s.
ABclonal:Immunofluorescence - P-cadherin Rabbit mAb (A25549)}

Immunofluorescence - P-cadherin Rabbit mAb (A25549)

Confocal immunofluorescence analysis of A-431 cells using P-cadherin Rabbit mAb (A25549, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). The cells were counterstained with α-Tubulin Mouse mAb (AC012, dilution 1:400) followed by incubation with ABflo® 488-conjugated Goat Anti-Mouse IgG (H+L) Ab (AS076, dilution 1:500) (Green). DAPI was used for nuclear staining (Blue). Objective: 100x.
ABclonal:Immunofluorescence - P-cadherin Rabbit mAb (A25549)}

Immunofluorescence - P-cadherin Rabbit mAb (A25549)

Confocal imaging of paraffin-embedded Human breast cancer tissue using P-cadherin Rabbit mAb (A25549, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval with 0.01 M citrate buffer (pH 6.0) prior to IF staining. Objective: 40x.
ABclonal:Flow CytoMetry - P-cadherin Rabbit mAb (A25549)}

Flow CytoMetry - P-cadherin Rabbit mAb (A25549)

Flow cytometry: 1X10^6 MCF7 cells (Low Expression, left) and A-431 cells (right) were surface-stained with P-cadherin Rabbit mAb (A25549, 2 μg/mL, orange line) or ABflo® 647 Rabbit IgG isotype control (A22070, 5 μl/Test, blue line), followed by Alexa Fluor® 647 conjugated goat anti-rabbit pAb staining. Non-fluorescently stained cells were used as blank control (red line).
ABclonal:Flow CytoMetry - P-cadherin Rabbit mAb (A25549)}

Flow CytoMetry - P-cadherin Rabbit mAb (A25549)

Flow cytometry: 1X10^6 A-431 cells were surface-stained with ABflo® 647 Rabbit IgG isotype control (A22070, 5 μl/Test, left) or P-cadherin Rabbit mAb (A25549, 2 μg/mL, right).

* For research use only. Not for therapeutic or diagnostic purposes.

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