Nova1 expression in Human Breast Cancer lysate analyzed by western blot. Cells were lysed in RIPA buffer and 35µg protein was run per lane. Primary antibody incubation was performed with Anti-Nova1 Antibody (A83421) at 0.01µg/ml and detected by chemiluminescence.
Nova1 expression in HEK293 cell lysate analyzed by western blot. Cells were transfected to overexpress Nova1 and incubated with Anti-Nova1 Antibody (A83421). Control: Mock-transfected HEK293 cell lysate incubated with Anti-Nova1 Antibody (A83421) (first lane).
Nova1 expression in Human Cortex analyzed by immunohistochemistry. Tissue was paraffin-embedded, and antigen retrieval was achieved by steaming in citrate buffer, pH 6. Staining was performed with Anti-Nova1 Antibody (A83421) at 5µg/ml and revealed with alkaline phosphatase (AP).
Nova1 expression in Human Heart analyzed by immunohistochemistry. Tissue was paraffin-embedded, and antigen retrieval was achieved by steaming in citrate buffer, pH 6. Staining was performed with Anti-Nova1 Antibody (A83421) at 5µg/ml and revealed with alkaline phosphatase (AP).
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Proteins predicted to interact with Nova1
Predicted protein interactions based upon String database. Revelancy score correlates with probability of interaction.
