The POP2 antibody has been utilized to investigate POPDC2’s role in:
Cardiac Function: Localizing POPDC2 in human heart tissue to study its involvement in maintaining cardiac rhythm .
Ion Channel Regulation: Exploring POPDC2’s interaction with potassium channels (e.g., KCNK2) and its modulation via cAMP-binding .
Immunohistochemical Validation: Demonstrated strong staining in human heart muscle tissue, confirming POPDC2’s cardiac localization .
Functional Insights: Suggested POPDC2 enhances cell surface expression of KCNK2, thereby influencing electrical activity in cardiomyocytes .
While the antibody itself does not modulate biological activity, its target (POPDC2) functions as a regulatory protein:
cAMP-Binding: Mediates signaling pathways critical for heart rate regulation .
KCNK2 Modulation: Increases potassium channel density, stabilizing membrane potential in cardiac cells .
The POP2 antibody serves as a tool for:
Cardiovascular Research: Studying POPDC2’s role in arrhythmias or heart failure.
Therapeutic Development: Identifying POPDC2 as a potential target for modulating cardiac ion channel function .
Here’s a structured FAQ collection for researchers working with POP2 (POPDC2) antibodies, synthesized from peer-reviewed methodologies and technical guidelines:
Common pitfalls and solutions:
Fluorescence-minus-one (FMO) controls: Identify spillover between channels .
Voltration: Optimize PMT voltages to avoid signal saturation (e.g., peak 2 method) .
Biological controls: Compare wild-type vs. POP2-deficient cardiomyocytes .
Prepare serial dilutions (1:50 to 1:800) in PBS/1% BSA.
Stain POP2-positive cells (e.g., primary cardiomyocytes).
Select the dilution with the highest SI (typically 1:200 for ab224121 in IHC) .
Yes, but prioritize spectral overlap resolution:
| Marker | Fluorophore | Laser Compatibility |
|---|---|---|
| POP2 (ab224121) | AF488 | 488 nm |
| Troponin T | PE-Cy7 | 561 nm |
| Connexin 43 | BV421 | 405 nm |
Source: Panel design principles from .
Cause: Residual protein aggregates or incomplete blocking.
Solution: Pre-clear lysates with protein A/G beads and use 5% non-fat milk + 0.1% Tween-20 .