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RFP Antikörper

(Red Fluorescent Protein (RFP))
Antibodies that detect Red Fluorescent Protein (RFP) are used in various biological and biomedical research applications (e.g. Western Blot) to visualize and study cellular processes, protein localization, and gene expression. Red Fluorescent Protein is a type of fluorescent protein that emits red light when exposed to specific wavelengths of light. It's often used as a molecular tag to label proteins and other cellular structures in live or fixed cells and tissues. Here are some common applications of RFP antibodies:
  • 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.

69 Treffer

RFP Reaktivität: Discosoma Wirt: Kaninchen Monoclonal Alexa Fluor 647 Recombinant Antibody
Produktnummer ABIN6915187
 
RFP Reaktivität: Discosoma Wirt: Kaninchen Monoclonal Alexa Fluor 680 Recombinant Antibody
Produktnummer ABIN6904636
 
RFP Reaktivität: Discosoma Wirt: Kaninchen Monoclonal Alexa Fluor 750 Recombinant Antibody
Produktnummer ABIN6856446
 
RFP Reaktivität: Discosoma Wirt: Kaninchen Monoclonal Biotin Recombinant Antibody
Produktnummer ABIN6872510
 
RFP Reaktivität: Discosoma WB, ELISA, DB Wirt: Llama Monoclonal RFP40 unconjugated single-domain Antibody (sdAb) Recombinant Antibody
Produktnummer ABIN7565835
 
RFP Reaktivität: Discosoma WB, ELISA, FM Wirt: Ziege Polyclonal unconjugated
Produktnummer ABIN7565833
 
RFP Reaktivität: Discosoma WB, ELISA Wirt: Maus Monoclonal unconjugated
Produktnummer ABIN865861
 
RFP Reaktivität: Discosoma WB, ELISA Wirt: Maus Monoclonal unconjugated
Produktnummer ABIN865860
 
RFP Reaktivität: Discosoma WB, ELISA, IF Wirt: Kaninchen Polyclonal FITC
Produktnummer ABIN2349649
 
  • Typ Primary
    • Primary
  • Anwendung
    • Western Blotting (WB)
    • Immunofluorescence (IF)
    • ELISA
    • Immunocytochemistry (ICC)
    • Flow Cytometry (FACS)
    • Fluorescence Microscopy (FM)
    • Immunohistochemistry (IHC)
    • Immunoprecipitation (IP)
    • Immunohistochemistry (Frozen Sections) (IHC (fro))
    • Dot Blot (DB)
    • Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    • FLISA
    • Immunochromatography (IC)
  • Reaktivität
    • Discosoma
    • Various Species
  • In Publikationen zitiert
  • Abbildungen verfügbar
  • Independent Validation
  • Nur ohne Konservierungsmittel
  • Carrier free only
  • Wirt
    • Rabbit
    • Mouse
    • Alpaca
    • Goat
    • Chicken
    • Llama
  • Klonalität
    • Monoclonal
    • Polyclonal
  • Klon
    • 2B12
    • 2B12-2A1
    • 3G5
    • 8E5-G7
    • RF5R
    • 115D6
    • 1DS-1A6
    • 1G11
    • 25
    • 8D6
    • 8H2
    • E64-1077
    • RFP40
    • SAA1152
  • Bindungsspezifität
    • AA 21-245
    • N-Term
    • AA 22-36
  • Konjugat
    • Unkonjugiert
    • Biotin
    • Alexa Fluor 647
    • AZDye 568
    • Agarose Beads
    • Alexa Fluor 488
    • Alexa Fluor 555
    • Alexa Fluor 594
    • Alexa Fluor 680
    • Alexa Fluor 750
    • Atto 488
    • FITC
    • Alexa Fluor 350
    • Alexa Fluor 405
    • DBCO
    • DyLight 405
    • DyLight 488
    • DyLight 550
    • DyLight 633
    • HRP
  • Isotyp
    • IgG
    • IgG1
    • IgG2a
    • IgG2a kappa
    • IgG2b
    • IgY
  • Protein-Typ
    • Recombinant Antibody
  • Format
    • Liquid
    • Lyophilized
  • Fragment
    • single-domain Antibody (sdAb)
  • Hersteller
    • antibodies-online
    • Signalway
    • Rockland
    • Acris
    • Enogene Biotech
    • ProteoGenix
    • USBio
    • BD Biosciences
    • Synaptic Systems

Aktuelle Publikationen für unsere RFP Antikörper

He, Boraas, Bell, Gong, Iannaccone, Wen, Mak, Carlson, Sumigray, Nicoli: "Epidermal Stem Cells Control Periderm Injury Repair via Matrix-Driven Specialization of Intercellular Junctions." in: bioRxiv : the preprint server for biology, (2025) (PubMed).

He, Boraas, Bell, Gong, Iannaccone, Wen, Mak, Carlson, Sumigray, Nicoli: "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).

Clements, Tang, Florjanic Baronik, Simpson Ragdale, Oria, Volteras, White, Beattie, Uddin, Lenn, Lindsay, Castro Devesa, Karamched, Lythgoe, Shahrezaei, Weaver, Sugisawa, Roncaroli, Marguerat, Hill, Parrinello: "Axonal injury is a targetable driver of glioblastoma progression." in: Nature, Vol. 646, Issue 8084, pp. 452-461, (2025) (PubMed).

He, Wang, Wang, Wang, Yang, Chen, Pei, Bai, Li, Wu, Chen: "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).

Zhou, Ghersi, Ristori, Semanchik, Prendergast, Zhang, Carneiro, Baldissera, Sessa, Nicoli: "Akt is a mediator of artery specification during zebrafish development." in: Development (Cambridge, England), Vol. 151, Issue 17, (2024) (PubMed).

Tanaka, Chen, Prendergast, Zhuang, Nasiri, Joshi, Hintzen, Chung, Kumar, Mani, Koleske, Crawford, Nicoli, Schwartz: "Latrophilin-2 mediates fluid shear stress mechanotransduction at endothelial junctions." in: The EMBO journal, Vol. 43, Issue 15, pp. 3175-3191, (2024) (PubMed).

Ghersi, Baldissera, Hintzen, Luff, Cheng, Xia, Sturgeon, Nicoli: "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).

Krishna, Choudhury, Keough, Seo, Ni, Kakaizada, Lee, Aabedi, Popova, Lipkin, Cao, Nava Gonzales, Sudharshan, Egladyous, Almeida, Zhang, Molinaro, Venkatesh, Daniel, Shamardani, Hyer, Chang, Findlay, Phillips, Nagarajan, Raleigh, Brang, Monje, Hervey-Jumpe: "Glioblastoma remodelling of human neural circuits decreases survival." in: Nature, Vol. 617, Issue 7961, pp. 599-607, (2023) (PubMed).

Lee, Ciabatti, González-Rueda, Williams, Nugent, Mookerjee, Morgese, Tripodi: "Combining long-term circuit mapping and network transcriptomics with SiR-N2c." in: Nature methods, Vol. 20, Issue 4, pp. 580-589, (2023) (PubMed).

Drexler, Khatri, Sauvigny, Mohme, Maire, Ryba, Zghaibeh, Dührsen, Salviano-Silva, Lamszus, Westphal, Gempt, Wefers, Neumann, Bode, Hausmann, Huber, Bonn, Jütten, Delev, Weber, Harter, Onken, Vajkoczy, Capper, Wiestler, Weller, Snijder, Buck, Weiss, Keough: "Epigenetic neural glioblastoma enhances synaptic integration and predicts therapeutic vulnerability." in: bioRxiv : the preprint server for biology, (2023) (PubMed).

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