Alexa Fluor™ 488 Tyramide SuperBoost™ Kit, streptavidin
Alexa Fluor™ 488 Tyramide SuperBoost™ Kit, streptavidin
Invitrogen™

Alexa Fluor™ 488 Tyramide SuperBoost™ Kit, streptavidin

SuperBoost™ tyramide signal amplification is the most sensitive method for detection of low abundant targets in multiplexable fluorescent immunocytochemistry (ICC),深入閱讀
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產品號碼Quantity
B40932150 Slides
產品號碼 B40932
價格 (HKD)
6,934.00
Each
新增至購物車
Quantity:
150 Slides
價格 (HKD)
6,934.00
Each
新增至購物車
SuperBoost™ tyramide signal amplification is the most sensitive method for detection of low abundant targets in multiplexable fluorescent immunocytochemistry (ICC), immunohistochemistry (IHC ), and in situ hybridization (ISH). SuperBoost kits combine the brightness of AlexaFluor™ dyes with the superior signal amplification of a poly-HRP-mediated tyramide labeling reaction to produce a sensitivity 10-200 times greater than standard methods. For standout research, SuperBoost kits sharpen your results for clear visibility into critical areas that standard imaging methods fail to reveal.

SuperBoost kits are simple to use and easily adapted to standard ICC, IHC, or FISH experimental protocols, using any cell or tissue type. Cells labeled using a SuperBoost kit can be imaged using any type of microscope, producing high-resolution multiplex images. This particular kit features AlexaFluor 488 tyramide (496/524 ex/em), detected using a standard Green/FITC/GFP filter cube. This kit also features HRP-conjugated streptavidin.

Features of the SuperBoost kits include:
• Superior sensitivity for detection of low-level or hard-to-detect targets by fluorescent imaging
• Simple protocol and detection using standard filters
• Suitable for high-resolution multiplex images—co-label with DAPI, secondary antibodies, and other SuperBoost kits
• Requires 10-100 times less primary antibody then standard ICC/IHC/ISH experiments

SuperBoost kits are based on the tyramide signal amplification system, which uses the catalytic activity of horseradish peroxidase (HRP) to generate high density labeling of a target protein or nucleic acid sequence in situ. A typical ICC/IHC/ISH experiment using a SuperBoost kit requires 10-100 times less primary antibody then standard ICC/IHC/ISH experiments. SuperBoost kits offer superior specific signal intensity over background, so the protocol is easily optimized to detect specific signal in samples where high endogenous autofluorescence is observed.

Benefits of SuperBoost kits

Enhancement of signal using Alexa Fluor tyramides: SuperBoost kits utilize Alexa Fluor tyramides, which react with HRP to ultimately deposit bright and photostable Alexa Fluor dye on surrounding proteins and other similar molecules. SuperBoost kits are the only kits that combine the brightness of Alexa Fluor dyes with the enhancement of tyramide signal amplification to produce a superior signal.

Reaction stop solution: Like any enzyme-based labeling system, it is possible to overdevelop the signal. SuperBoost kits include an HRP stop solution to halt the HRP reaction. HRP stop solution can be used to obtain maximum signal, without increase of background signal. Images produced with optimized HRP reaction times are as sharp as images produced with standard ICC/IHC/ISH methods, but with 10-200 times more sensitivity.

Reduction of background: SuperBoost kits include blockers for the elimination or reduction of endogenous peroxidase and fluorescent background signals. These blockers help ensure that only specific signals are enhanced while keeping non-specific/background signals in check.

For Research Use Only. Not for use in diagnostic procedures.
規格
Product TypeTyramide Kit
Quantity150 Slides
Shipping ConditionApproved for shipment at Room Temperature or on Wet Ice
ConjugateAlexa Fluor 488
Product LineSuperBoost
Unit SizeEach
內容物與存放
1 kit sufficient for 150 microscope slides (18 x 18 mm), containing: Blocking buffer (1 X), 22.5 mL
  • HRP-conjugated streptavidin (1 X), 22.5 mL
  • Alexa Fluor tyramide reagent
  • Hydrogen peroxide (stabilized 3% soluti
  • 常見問答集 (常見問題)

    With a SuperBoost tyramide kit, I got excessive and non-specific labeling. What can I do to limit background and acquire a more localized labeling?

    To limit background, we recommend performing a pre-blocking step with 3% H2O2 for 60 mins to inactivate endogenous peroxidases. To limit the localization of labeling, we recommend optimizing the final concentration of the primary and secondary antibodies and the dye-tyramide. You may also limit the incubation time of the dye-tyramide on the sample.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    Is it possible to perform dual TSA labeling with SuperBoost tyramide kits?

    Yes. This involves the sequential application of the antibodies and the tyramides with a HRP-quenching step between antibodies using H2O2.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    How are SuperBoost tyramide kits different from the original TSA labeling kits?

    The SuperBoost tyramide kits utilize poly-HRP labeled antibodies. This provides a greater number of horseradish peroxidase (HRP) molecules per antibody. The original kits used antibodies and streptavidin that were directly conjugated with HRP and thus, limited the number per antibody or streptavidin.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    引用資料與參考文獻 (2)

    引用資料與參考文獻
    Abstract
    Sensitive immunofluorescent staining of cells via generation of fluorescent nanoscale polymer films in response to biorecognition.
    Authors:Avens HJ, Berron BJ, May AM, Voigt KR, Seedorf GJ, Balasubramaniam V, Bowman CN
    Journal:J Histochem Cytochem
    PubMed ID:21339175
    Immunofluorescent staining is central to nearly all cell-based research, yet only a few fluorescent signal amplification approaches for cell staining exist, each with distinct limitations. Here, the authors present a novel, fluorescent polymerization-based amplification (FPBA) method that is shown to enable similar signal intensities as the highly sensitive, enzyme-based tyramide ... More
    FGF23 is synthesised locally by renal tubules and activates injury-primed fibroblasts.
    Authors:Smith ER, Tan SJ, Holt SG, Hewitson TD,
    Journal:Sci Rep
    PubMed ID:28611350
    In kidney disease, higher circulating levels of the mineral-regulating hormone fibroblast growth factor (FGF)-23 are predictive of disease progression but direct pathogenic effects on the kidney are unknown. We sought evidence of local renal synthesis in response to unilateral ureteric obstruction in the mouse, and pro-fibrotic actions of FGF23 on ... More