Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

RFP-Booster (Atto 594) Accessory Reagents

With our Booster you reactivate, boost, stabilizate the signals of your fusion proteins.
Pubmed (18)
Catalog No. ABIN1082216
$371.25
Plus shipping costs $45.00
100 μL ABIN1082216
100 μL ABIN1082216
local_shipping Shipping to: United States
Delivery in 5 to 6 Business Days
  • Target Name (Antigen)
    Antibody Type
    Recombinant Antibody
    Reactivity
    Discosoma
    Conjugate
    Atto 594
    Application
    Fluorescence Microscopy (FM), Immunofluorescence (IF)
    Purpose
    With our Booster you reactivate, boost, stabilizate the signals of your fusion proteins.
    Specificity
    RFP-Booster efficiently highlights, enhancesand stabilizes monomeric red fluorescentproteins such as mRFP1, mCherry or mPlum but also mRuby
    Characteristics
    • Enhance, stabilize and reactivate your fl uorescent proteins
    • RFP-Booster high specifi city for various monomeric red fl uorescent proteins derived from DsRed
    • Coupled to bright and photostable chemical dyes from ATTO-TEC
    Components
    RFP-Trap® coupled to fluorescent dye ATTO 594
    Featured
    Discover our best selling RFP Primary Antibody
  • Application Notes
    For the immunofluorescence staining of RFP-fusion proteins in fixed cells
    Comment

    Booster are very small, highly specific GFP- or RFP-binding proteins covalently coupled to the superior fluorescent dyes from ATTO-TEC.

    Assay Procedure
    • 1. Fixation: 4% paraformaldehyde (PFA) or 1:10 formalin (37% formaldehyde, 10-15% MetOH) in PBS, 10 min., RT.
    • 2. Wash 3x with PBS containing 0.1% Tween 20 (PBST). Critical: do not let coverslips “dry”.
    • 3. Permeabilisation: PBS containing 0.5% Triton X-100, 5 min., RT. Alternatively, permeabilise by incubating in 100% methanol for 5 min at -20°C.
    • 4. Wash 2x with PBST.
    • 5. Blocking: 4% BSA in PBST, 10 min, RT.
    • 6. RFP-Booster incubation: dilute RFP-Booster 1:200 – 1:400 in blocking buffer and incubate 1 h, RT.
      Note: For multiplexing protocols you can combine RFP-Booster with any other antibody.
    • 7. Wash 3x 5-10 min in PBST.
    • 8. If required, counterstain with DNA fluorescent dyes, e.g. DAPI.
    • 9. Before mounting, coverslips can be very briefly rinsed in water to prevent salt crystals to form.
    • 10. Mount in VectaShield (Vector Labs) or other mounting media with anti-fading agents and seal mounted coverslips with clear nail polish.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.2 mg/ml
    Buffer
    PBS, 0.01% Sodium azide
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Do not freeze. Protect from light.
    Storage
    4 °C
    Expiry Date
    6 months
  • Pentakota, Zhou, Smith, Maffini, Petrovic, Morgan, Weir, Vetter, Musacchio, Luger: "Decoding the centromeric nucleosome through CENP-N." in: eLife, Vol. 6, 2018 (PubMed).

    Anton, Bultmann: "Site-specific recruitment of epigenetic factors with a modular CRISPR/Cas system." in: Nucleus (Austin, Tex.), Vol. 8, Issue 3, pp. 279-286, 2018 (PubMed).

    Natsume, Nishimura, Minocherhomji, Bhowmick, Hickson, Kanemaki: "Acute inactivation of the replicative helicase in human cells triggers MCM8-9-dependent DNA synthesis." in: Genes & development, Vol. 31, Issue 8, pp. 816-829, 2017 (PubMed).

    Winter, Loidolt, Westphal, Butkevich, Gregor, Sahl, Hell: "Multicolour nanoscopy of fixed and living cells with a single STED beam and hyperspectral detection." in: Scientific reports, Vol. 7, pp. 46492, 2017 (PubMed).

    Vietri, Schink, Campsteijn, Wegner, Schultz, Christ, Thoresen, Brech, Raiborg, Stenmark: "Spastin and ESCRT-III coordinate mitotic spindle disassembly and nuclear envelope sealing." in: Nature, Vol. 522, Issue 7555, pp. 231-5, 2015 (PubMed).

    Osterfield, Schüpbach, Wieschaus, Shvartsman: "Diversity of epithelial morphogenesis during eggshell formation in drosophilids." in: Development (Cambridge, England), Vol. 142, Issue 11, pp. 1971-7, 2015 (PubMed).

    Platonova, Winterflood, Junemann, Albrecht, Faix, Ewers: "Single-molecule microscopy of molecules tagged with GFP or RFP derivatives in mammalian cells using nanobody binders." in: Methods (San Diego, Calif.), 2015 (PubMed).

    Biermann, Sokoll, Klueva, Missler, Wiegert, Sibarita, Heine: "Imaging of molecular surface dynamics in brain slices using single-particle tracking." in: Nature communications, Vol. 5, pp. 3024, 2014 (PubMed).

    Bleck, Itano, Johnson, Thomas, North, Bieniasz, Simon: "Temporal and spatial organization of ESCRT protein recruitment during HIV-1 budding." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 111, Issue 33, pp. 12211-6, 2014 (PubMed).

    Winterflood, Ewers: "Single-Molecule Localization Microscopy using mCherry." in: Chemphyschem : a European journal of chemical physics and physical chemistry, Vol. 15, Issue 16, pp. 3447-51, 2014 (PubMed).

    Hasegawa, Ryu, Kaláb: "Chromosomal gain promotes formation of a steep RanGTP gradient that drives mitosis in aneuploid cells." in: The Journal of cell biology, Vol. 200, Issue 2, pp. 151-61, 2013 (PubMed).

    Franz, Roque, Saurya, Dobbelaere, Raff: "CP110 exhibits novel regulatory activities during centriole assembly in Drosophila." in: The Journal of cell biology, Vol. 203, Issue 5, pp. 785-99, 2013 (PubMed).

    Ridzuan, Moon, Knuepfer, Black, Holder, Green: "Subcellular location, phosphorylation and assembly into the motor complex of GAP45 during Plasmodium falciparum schizont development." in: PLoS ONE, Vol. 7, Issue 3, pp. e33845, 2012 (PubMed).

    Mikeladze-Dvali, von Tobel, Strnad, Knott, Leonhardt, Schermelleh, Gönczy: "Analysis of centriole elimination during C. elegans oogenesis." in: Development (Cambridge, England), Vol. 139, Issue 9, pp. 1670-9, 2012 (PubMed).

    Ries, Kaplan, Platonova, Eghlidi, Ewers: "A simple, versatile method for GFP-based super-resolution microscopy via nanobodies." in: Nature methods, Vol. 9, Issue 6, pp. 582-4, 2012 (PubMed).

    Weil, Parton, Herpers, Soetaert, Veenendaal, Xanthakis, Dobbie, Halstead, Hayashi, Rabouille, Davis: "Drosophila patterning is established by differential association of mRNAs with P bodies." in: Nature cell biology, Vol. 14, Issue 12, pp. 1305-13, 2012 (PubMed).

    Cordes, Maiser, Steinhauer, Schermelleh, Tinnefeld: "Mechanisms and advancement of antifading agents for fluorescence microscopy and single-molecule spectroscopy." in: Physical chemistry chemical physics : PCCP, Vol. 13, Issue 14, pp. 6699-709, 2011 (PubMed).

    Guizetti, Schermelleh, Mäntler, Maar, Poser, Leonhardt, Müller-Reichert, Gerlich: "Cortical constriction during abscission involves helices of ESCRT-III-dependent filaments." in: Science (New York, N.Y.), Vol. 331, Issue 6024, pp. 1616-20, 2011 (PubMed).

  • Target Name (Antigen)
    Alternative Name
    RFP
    Background
    Red fluorescent proteins (RFP) and variants thereof are widely used to study protein localization and dynamics in living cells. However, photo stability and quantum efficiency of RFP are not sufficient for Super-Resolution Microscopy (e.g. 3D-SIM or STED) of fixed samples. In addition, many cell biological methods such as BrdU-staining, EdU-Click-iT™ treatment or Fluorescent In Situ Hybridization result in disruption of the RFP signal.The RFP-Booster_Atto594, a specific RFP-binding protein coupled to the fluorescent dye ATTO 594, reactivates, boosts and stabilizes your RFP signal.
You are here: