Qdot™ 565 Streptavidin Conjugate
Invitrogen™

Qdot™ 565 Streptavidin Conjugate

Qdot™ 565 streptavidin conjugate comprises a biotin-binding protein (streptavidin) covalently attached to a fluorescent label (Qdot™ nanocrystal). Streptavidin has aRead more
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Catalog NumberQuantity
Q10131MP200 μL
Q10133MP50 μL
Catalog number Q10131MP
Price (TWD)
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Quantity:
200 μL
Price (TWD)
***
Qdot™ 565 streptavidin conjugate comprises a biotin-binding protein (streptavidin) covalently attached to a fluorescent label (Qdot™ nanocrystal). Streptavidin has a very high binding affinity for biotin, and a conjugate of streptavidin is commonly used together with a conjugate of biotin for specific detection of a variety of proteins, protein motifs, nucleic acids, and other molecules (for example, a biotinylated primary antibody bound to a protein target can be detected with a fluorescently labeled streptavidin). Strategies similar to this are used in many detection protocols including western blots, flow cytometry, imaging and microscopy, and microplate assays, and are also used in purification workflows to achieve targeted fractionation. Qdot™ nanocrystal conjugates are provided as 1 μM solutions.

Important Features of Qdot™ Streptavidin Conjugates:
Streptavidin Qdot™ 565 conjugate has emission maxima of ∼565 nm
Approximately 5 to 10 streptavidins per Qdot™ nanocrystal
Extremely photostable and bright fluorescence
Efficiently excited with single-line excitation sources
Narrow emission, large Stokes shift
Available in multiple colors
Ideal for western blots, flow cytometry, imaging and microscopy, microplate assays and more

Properties of Qdot™ Nanocrystals
The Qdot™ streptavidin conjugate is the size of a large macromolecule or protein (∼15–20 nm) and represents the brightest class of streptavidin detection reagents. Qdot™ streptavidin conjugates are made from a nanometer-scale crystal of a semiconductor material (CdSe), which is coated with an additional semiconductor shell (ZnS) to improve the optical properties of the material. The Qdot™ 705 and Qdot™ 800 streptavidin conjugates, which include CdSeTe, are made in a similar fashion. This core-shell material is further coated with a polymer shell that allows the materials to be conjugated to biological molecules and to retain their optical properties.

Other Fluorescent Conjugates of Streptavidin are Available
We offer several other Qdot™ colors or try the Qdot™ Streptavidin Sampler Kit, containing Qdot™ streptavidin conjugates in six colors 525, 565, 585, 605, 655, and 705. In addition to nanocrystal conjugates, we offer a wide range of streptavidins conjugated to Alexa Fluor™ dyes, Oregon Green™ dye, enzyme conjugates, and traditional fluorophores like Texas Red™ dye, fluorescein (FITC) and more.

Find Biotinylated Conjugates
We offer an extensive line of biotinylated conjugates for use in biotin-streptavidin detection strategies.
• Use the primary antibody search tool to find biotinylated primary antibodies
• Use the secondary antibody selector tool to find biotinylated secondary antibodies and biotinylated anti-dye and anti-hapten antibodies

Blocking Endogenous Biotin
Naturally occurring biotins can interfere with biotin-streptavidin detection schemes. For experiments involving fixed and permeabilized cells, try our Endogenous Biotin-Blocking Kit to minimize this interference.

For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use.

Related Links:

Learn more about Avidin-Biotin Detection

To learn more about Qdot™ Nanocrystals
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Concentration1 μM
Product TypeStreptavidin Conjugate (fluorescent)
Quantity200 μL
Shipping ConditionRoom Temperature
ConjugateQdot 565
FormLiquid
Product LineQdot
Unit SizeEach
Contents & Storage
Store in refrigerator (2–8°C).

Citations & References (13)

Citations & References
Abstract
Random walk of processive, quantum dot-labeled myosin Va molecules within the actin cortex of COS-7 cells.
Authors:Nelson SR, Ali MY, Trybus KM, Warshaw DM,
Journal:Biophys J
PubMed ID:19619465
'Myosin Va (myoVa) is an actin-based intracellular cargo transporter. In vitro experiments have established that a single myoVa moves processively along actin tracks, but less is known about how this motor operates within cells. Here we track the movement of a quantum dot (Qdot)-labeled myoVa HMM in COS-7 cells using ... More
The human herpesvirus 8 chemokine receptor vGPCR triggers autonomous proliferation of endothelial cells.
Authors:Grisotto MG, Garin A, Martin AP, Jensen KK, Chan P, Sealfon SC, Lira SA
Journal:J Clin Invest
PubMed ID:16604194
'We have used a novel conditional transgenic system to study the mechanisms of angioproliferation induced by viral G protein-coupled receptor (vGPCR), the constitutively active chemokine receptor encoded by human herpesvirus 8 (HHV8, also known as Kaposi sarcoma herpesvirus). Using this system, we were able to control temporal expression of vGPCR ... More
Parallel detection of antigen-specific T-cell responses by multidimensional encoding of MHC multimers.
Authors:Hadrup SR, Bakker AH, Shu CJ, Andersen RS, van Veluw J, Hombrink P, Castermans E, Thor Straten P, Blank C, Haanen JB, Heemskerk MH, Schumacher TN,
Journal:Nat Methods
PubMed ID:19543285
'The use of fluorescently labeled major histocompatibility complex multimers has become an essential technique for analyzing disease- and therapy-induced T-cell immunity. Whereas classical major histocompatibility complex multimer analyses are well-suited for the detection of immune responses to a few epitopes, limitations on human-subject sample size preclude a comprehensive analysis of ... More
Reaching out for signals: filopodia sense EGF and respond by directed retrograde transport of activated receptors.
Authors:Lidke DS, Lidke KA, Rieger B, Jovin TM, Arndt-Jovin DJ
Journal:J Cell Biol
PubMed ID:16103229
'ErbB1 receptors situated on cellular filopodia undergo systematic retrograde transport after binding of the epidermal growth factor (EGF) and activation of the receptor tyrosine kinase. Specific inhibitors of the erbB1 receptor tyrosine kinase as well as cytochalasin D, a disruptor of the actin cytoskeleton, abolish transport but not free diffusion ... More
Analysis of UV-excited fluorochromes by flow cytometry using near-ultraviolet laser diodes.
Authors:Telford WG
Journal:Cytometry A
PubMed ID:15351984
'INTRODUCTION: Violet laser diodes have become common and reliable laser sources for benchtop flow cytometers. While these lasers are very useful for a variety of violet and some ultraviolet-excited fluorochromes (e.g., DAPI), they do not efficiently excite most UV-stimulated probes. In this study, the next generation of InGaN near-UV laser ... More