H Cadherin was immunoprecipitated using 0.5mg NIH3T3 whole cell extract, 5µg of Rabbit polyclonal to H Cadherin and 50µl of protein G magnetic beads (+). No antibody was added to the control (-).The antibody was incubated under agitation with Protein G beads for 10min, NIH3T3 whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70°C; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab36905.Secondary: Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697).Band: 78kDa; H Cadherin.
Lane 1 : Anti-H Cadherin antibody (ab36905) at 0.5 µg/mlLane 2 : Anti-H Cadherin antibody (ab36905) at 1 µg/mlLane 1 : 3T3 cell lysate.Lane 2 : 3T3 cell lysate.
ab36905 at 20µg/ml staining H Cadherin in K562 cells by ICC/IF
ab36905 staining H Cadherin in human kidney tissue by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections).Tissue was fixed in paraformaldehyde and an antigen retrieval step was performed using TRIS-EDTA Buffer pH 9.0. Cells were then permeabilized and incubated with ab36905 at a 1/1000 dilution for 30 minutes at 20°C. The secondary used was an undiluted HRP conjugated goat polyclonal.See Abreview