RFP-Booster (Atto 594)

ABIN1082216 产品详细信息, 供应商: Log in to see
  • RFP
  • RNF76
  • tripartite motif containing 27
  • TRIM27
Recombinant Antibody
Atto 594
Fluorescence Microscopy (FM), Immunofluorescence (IF)
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Supplier Product No.
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原理 With our Booster you reactivate, boost, stabilizate the signals of your fusion proteins.
特异性 RFP-Booster efficiently highlights, enhancesand stabilizes monomeric red fluorescentproteins such as mRFP1, mCherry or mPlum but also mRuby
  • 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
组件 RFP-Trap® coupled to fluorescent dye ATTO 594
别名 RFP
背景 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.
应用备注 For the immunofluorescence staining of RFP-fusion proteins in fixed cells

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

  • 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.
限制 仅限研究用
状态 Liquid
浓度 0.2 mg/ml
缓冲液 PBS, 0.01% Sodium azide
储存液 Sodium azide
注意事项 This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
注意事项 Do not freeze. Protect from light.
储存条件 4 °C
有效期 6 months
 image for RFP-Booster (Atto 594) (ABIN1082216) RFP-Booster specifically labels RFP-fusion proteins. HeLa cells expressing mRFP-PCNA,...
 image for RFP-Booster (Atto 594) (ABIN1082216) Enhancement of RFP signal with RFP-Booster_Atto594. Comparison of signal intensity of...
 image for RFP-Booster (Atto 594) (ABIN1082216) Improvement of RFP signal stability with RFP-Booster_Atto594. RFP fluorescence bleach...
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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).

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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).

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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).