The FtsZ2-1 Antibody is a polyclonal rabbit antibody specifically designed to detect the FtsZ2-1 protein, a homolog of bacterial FtsZ critical for chloroplast division in plants. This antibody targets the conserved regions of FtsZ2-1, enabling precise localization and quantification in experimental systems. Its primary applications include Western blotting, immunoprecipitation, and immunofluorescence, with validation across diverse plant species .
The FtsZ2-1 Antibody demonstrates high specificity for Arabidopsis thaliana and Hordeum vulgare, with predicted reactivity in other plant species, including Glycine max, Ricinus communis, and Populus trichocarpa .
| Species | Reactivity | Source |
|---|---|---|
| Arabidopsis thaliana | Confirmed | |
| Hordeum vulgare | Confirmed | |
| Glycine max | Predicted | |
| Populus trichocarpa | Predicted |
The antibody does not cross-react with bacterial FtsZ or tubulin-like proteins . Competitive immunoblot assays confirm its specificity, as pre-incubation with recombinant FtsZ2-1 blocks signal detection, while FtsZ1-1 does not .
The FtsZ2-1 Antibody is optimized for Western blotting at a dilution of 1:2000, detecting a band of ~50.7 kDa (expected apparent molecular weight) . Example protocols include:
Sample Preparation: Separation of recombinant FtsZ2-1 (~10 kDa) or plant extracts on 4–12% LDS-PAGE.
Detection: Blocking with 2% low-fat milk, probing with the antibody, and signal development using HRP-conjugated secondary antibodies .
Used in Physcomitrella to confirm in vivo interactions between FtsZ2-1 and FtsZ1 isoforms. GFP-tagged FtsZ2-1 was immunoprecipitated, and interacting partners were identified via mass spectrometry .
Dual-labeling studies in Arabidopsis reveal colocalization of FtsZ2-1 and FtsZ1-1 at mid-chloroplast rings, critical for plastid division .
Studies in Arabidopsis demonstrate that FtsZ2-1 and FtsZ2-2 are functionally redundant for chloroplast division, while FtsZ1 is non-redundant. Overexpression of either FtsZ2 isoform rescues division defects in null mutants, but replacement of FtsZ1 with FtsZ2 fails to restore normal plastid numbers .
In Physcomitrella, FtsZ2-1 interacts with FtsZ1-2 in vitro and in vivo, enhancing GTPase activity and polymerization rates. This synergistic interaction is distinct from bacterial FtsZ dynamics .
FtsZ2-1 is essential for plastid division in higher plants. Overexpression disrupts division, while antisense suppression reduces plastid numbers. The antibody has been pivotal in tracking FtsZ2-1 levels during these experiments .
FtsZ2-1 shares structural homology with bacterial FtsZ but lacks motor proteins. Its function in plants suggests a conserved mechanism of cytoskeletal ring formation for organelle division .
This antibody targets FtsZ2-1, a protein exhibiting GTPase activity. It is a critical component of the plastid division machinery, forming a contractile ring at the division site. FtsZ2-1's role in plastid division is dose-dependent.
FtsZ2-1 Function and Regulation: The following research highlights key aspects of FtsZ2-1's function and regulation within the context of plastid division: