RFP 抗体
- Cellular Localization and Protein Trafficking: Researchers can fuse the RFP protein to their protein of interest. By using an RFP antibody, they can detect the presence and subcellular localization of the fusion protein within cells. This helps in understanding the dynamics and movement of proteins within cellular compartments.
- Gene Expression Studies: RFP can also be used as a marker for gene expression. Researchers can use RFP-tagged constructs to monitor the expression of specific genes. Antibodies against RFP are then used to detect the RFP-tagged protein produced from these genes.
- Protein Interaction Studies: RFP can be used in protein-protein interaction studies. Proteins of interest are tagged with RFP and their interactions with other proteins are investigated. Antibodies against RFP can then be used to detect these interactions either through immunoprecipitation or other methods.
- Live Cell Imaging: RFP-tagged proteins can be imaged in real-time within live cells using fluorescence microscopy. This allows researchers to track protein dynamics, localization changes, and cellular responses in real-time.
- Flow Cytometry: Antibodies against RFP can be used in flow cytometry (FACS) to quantify the expression levels of RFP-tagged proteins in a population of cells. This is particularly useful for high-throughput studies.
- High-Content Screening: RFP antibodies can be used in high-content screening assays to study various cellular processes and responses across large sets of conditions or compounds.
- Visualization of Cellular Structures: RFP can be fused to specific cellular structures such as organelles, cytoskeletal components, or membranes. Antibodies against RFP allow researchers to visualize these structures and their dynamics.
- Co-localization Studies: Antibodies against RFP can be used in combination with antibodies against other fluorescent proteins to study co-localization and potential interactions between different cellular components.
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Latest Publications for our RFP 抗体
: "Epidermal Stem Cells Control Periderm Injury Repair via Matrix-Driven Specialization of Intercellular Junctions." in: bioRxiv : the preprint server for biology, (2025) (PubMed).: "Epidermal stem cells control periderm injury repair via matrix-driven specialization of intercellular junctions." in: Nature communications, Vol. 16, Issue 1, pp. 8967, (2025) (PubMed).
: "Axonal injury is a targetable driver of glioblastoma progression." in: Nature, Vol. 646, Issue 8084, pp. 452-461, (2025) (PubMed).
: "NeuroD1 Regulated Endothelial Gene Expression to Modulate Transduction of AAV-PHP.eB and Recovery Progress after Ischemic Stroke." in: Aging and disease, Vol. 15, Issue 6, pp. 2632-2649, (2024) (PubMed).
: "Akt is a mediator of artery specification during zebrafish development." in: Development (Cambridge, England), Vol. 151, Issue 17, (2024) (PubMed).
: "Latrophilin-2 mediates fluid shear stress mechanotransduction at endothelial junctions." in: The EMBO journal, Vol. 43, Issue 15, pp. 3175-3191, (2024) (PubMed).
: "Haematopoietic stem and progenitor cell heterogeneity is inherited from the embryonic endothelium." in: Nature cell biology, Vol. 25, Issue 8, pp. 1135-1145, (2023) (PubMed).
: "Glioblastoma remodelling of human neural circuits decreases survival." in: Nature, Vol. 617, Issue 7961, pp. 599-607, (2023) (PubMed).
: "Combining long-term circuit mapping and network transcriptomics with SiR-N2c." in: Nature methods, Vol. 20, Issue 4, pp. 580-589, (2023) (PubMed).
: "Epigenetic neural glioblastoma enhances synaptic integration and predicts therapeutic vulnerability." in: bioRxiv : the preprint server for biology, (2023) (PubMed).
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