| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | Cdc42 effector protein 1;Binder of Rho GTPases 5;Serum protein MSE55;CDC42EP1;BORG5, CEP1, MSE55; |
| Cellular Localization | |
| Clonality | |
| Concentration | |
| Form | Liquid |
| Host | |
| Immunogen | A synthesized peptide derived from human PSMA2 |
| Isotype | |
| Molecular Weight | |
| Product Type | |
| Reactivity | |
| Reconstitution | |
| Storage | |
| Target | |
| UniProt # |
Overview
This product is an anti-PSMA2 antibody for target detection and characterization. Key identifiers include host species: Rabbit; Monoclonal; clone 22P51; isotype IgG; reactivity: Human,Mouse,Rat. Reported application contexts include WB, IHC, ICC, IF, Flow (as provided in the source record). Boster Bio Anti-PSMA2 Rabbit Monoclonal Antibody catalog # M08901-1. Tested in WB, IHC, ICC/IF, Flow Cytometry applications. This antibody reacts with Human, Mouse, Rat.
Key elements and design rationale
- Target: PSMA2 (Cdc42 effector protein 1).
- Antibody format: Monoclonal; clone 22P51; isotype IgG.
- Host: Rabbit.
- Species reactivity: Human,Mouse,Rat (confirm in your model system with appropriate controls).
This description is intended to help interpret the antibody design and the biological context of the target using the fields provided in the catalog record, alongside general experimental considerations.
Biological background
PSMA2 (protein: T-cell surface glycoprotein CD3 zeta chain) is a commonly studied target in molecular and cellular biology. Functional context (as provided): Probably involved in the organization of the actin cytoskeleton. Induced membrane extensions in fibroblasts. . Reported cellular localization context: Endomembrane system ; Peripheral membrane protein . Cytoplasm, cytoskeleton . Tissue expression notes (as provided): Endothelial and bone marrow stromal cells.
Research relevance and current trends
- Research context keywords from the source record include: Actin Assembly,Actin, etc.,Cytoskeleton,Cytoskeleton/ECM,Microfilaments,Signal Transduction.
- Current studies often focus on connecting target abundance/localization to pathway perturbations across models, tissues, and cell states.
- Quantitative and multiplexed assays (e.g., imaging + immunoblot panels) are commonly used to compare phenotypes across conditions and time-courses.
Common research applications
- Western blotting (WB): assess relative target abundance across samples, treatments, or time-points.
- Immunohistochemistry (IHC): evaluate spatial distribution of target-positive staining in tissue architecture.
- Immunofluorescence/ICC (IF/ICC): visualize subcellular localization patterns and cell-to-cell heterogeneity.
- Flow cytometry: quantify target-positive populations and compare shifts in marker distributions.
Workflow ideas (metafield): Validate PSMA2 antibody specificity using KO/KD control samples (WB/IF/IHC as appropriate), Detect PSMA2 expression by Western blot in cell or tissue lysates, Detect PSMA2 in FFPE tissue sections by immunohistochemistry, Localize PSMA2 by immunofluorescence/immunocytochemistry in cultured cells, Quantify PSMA2-positive cells by flow cytometry in single-cell suspensions
Notes for experimental interpretation
- Consider isoforms and post-translational modifications (PTMs) that may shift apparent molecular weight or epitope accessibility.
- Apparent molecular weight may vary by sample type and processing (observed MW: 26 kDa; calculated MW: 40295 MW).
- Control concepts: include appropriate negative controls (e.g., isotype, KO/KD samples) and orthogonal validation when feasible.
Additional product details (from the source record)
- Molecular weight (observed): 26 kDa
- Cellular localization (provided): Endomembrane system ; Peripheral membrane protein . Cytoplasm, cytoskeleton .
- Tissue details (provided): Endothelial and bone marrow stromal cells.
Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.
