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SBI/ExoGlow?-NTA Fluorescent Labeling Kit/EXONTA100A-1/10 Reactions

基因編輯
SBI/ExoGlow?-NTA Fluorescent Labeling Kit/EXONTA100A-1/10 Reactions


商品編號


EXONTA100A-1



品牌


SBI



公司


System Biosciences(SBI)



公司分類(lèi)


exosome labeling


商品信息

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Overview:
Just see extracellular vesicles with NanoSight

Making a great exosome research tool even better,
SBI
has developed ExoGlow
TM
-NTA, a proprietary dye that enables fluorescent NanoSight
TM
analysis* of only the extracellular vesicles present in a heterogenous sample. The result is more accurate EV NanoSight data that excludes protein aggregates, membrane fractions, and other background particles to provide EV-specific particle size and concentration.



The only commercially available kit that specifically labels EVs for fluorescent NanoSight NTA quantitation

Delivers high signal-to-noise ratio with a proprietary dye that specifically binds EVs

Validated using common EV isolation methods including as ExoQuick
TM
, ultracentrifugation, and column-based methods (see Supporting Data, Figure 1)

Optimized for a fast protocol that takes only 45 minutes from sample isolation to analysis


*For fluorescent NTA analysis, the NanoSight NTA system (model LM10, NS300 or others) MUST be installed and properly calibrated with a 488nm laser (available separately). Please contact your local Malvern Instruments representative for additional information.

How It Works:
Gain more accurate insight into your exosome sample


The ExoGlow-NTA Kit takes advantage of the fluorescence cap
ABI
lities of the NanoSight instrument* with a proprietary fluorescent dye, which works by binding specifically and efficiently to the surface of intact vesicles. Membrane fragments, protein aggregates, and other background particles do not bind the ExoGlow-NTA dye, resulting in exclusion of these species from fluorescent NTA analysis (Figure 1). Thus, with the ExoGlow-NTA Kit, the data delivered by NTA more accurately represents the EV populations in your sample rather than all particles, as is typically reported by conventional (non-fluorescent) NTA.


Figure 1. The ExoGlow-NTA dye only binds to membranes of intact EVs
. Unlike conventional NTA, which collects data on all particles in a solution based on light scattering, the fluorescence mode of the NanoSight instrument selectively detects the labeled EVs and only the data from fluorescently-labeled particles is reported.

The ExoGlow-NTA Fluorescent Labeling Kit comes with three components: 1) Labeling dye 2) Internal Standards and 3) Reaction Buffer. Simply mix the dye with the reaction buffer, add 1-100 ?g of EVs (or protein equivalent), incubate for 30 minutes, and you are ready for fluorescent NTA analysis. The provided Internal Standards are size-controlled synthetic
liposomes
that provide a positive control for NanoSight calibration as well as EV/exosome labeling efficiency using the ExoGlow-NTA Kit.

*For fluorescent NTA analysis, the NanoSight NTA system (model LM10, NS300 or others) MUST be installed and properly calibrated with a 488nm laser (available separately). Please contact your local Malvern Instruments representative for additional information.

Don’t have access to a NanoSight instrument equipped with the 488nm laser?
SBI
also offers fluorescent NTA as a service. Simply send us your samples, and we will isolate, label, and perform fluorescent NTA on your EVs. Email our Services department to request a quote now.

上一篇 SBI/pCT-CD9-GFP (pCMV, Exosome/Secretory, CD9 Tetraspanin Tag)/CYTO122-PA-1/10 ?g  下一篇 SBI/FluoroCet Exosome Quantitation Kit/FCET96A-1/96 Reactions

產(chǎn)品貨號:4100.0

4100.0 ¥
11至15個(gè)工作日送達
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