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Citations & References (17)
Invitrogen™
Qtracker™ 705 Vascular Labels
Qtracker™ non-targeted quantum dots are designed to be injected into the tail vein of mice for the study of vascularRead more
| Catalog Number | Quantity |
|---|---|
| Q21061MP | 200 μL |
Catalog number Q21061MP
Price (INR)
38,720.00
Online offer
Ends: 31-Dec-2025
70,398.00Save 31,678.00 (45%)
Each
Quantity:
200 μL
Price (INR)
38,720.00
Online offer
Ends: 31-Dec-2025
70,398.00Save 31,678.00 (45%)
Each
Qtracker™ non-targeted quantum dots are designed to be injected into the tail vein of mice for the study of vascular structure using small animal in vivo imaging (SAIVI) techniques. These nanocrystals exhibit intense fluorescence with red-shifted emission for increased tissue penetration, and have a PEG surface coating specially developed to minimize nonspecific interactions and reduce immune response by the tissue. Because the PEG surface coating does not contain reactive functional groups, the Qtracker™ non-targeted quantum dots are retained in circulation longer and can be imaged for up to 3 hours with a single injection or for longer periods of time with additional injections.
Need a different emission spectrum or longer tracking? View our other mammalian cell tracking products.
Key Attributes:
• Qtracker™ 705 label has Ex/Em (405-665/705) nm
• Designed for small animal in vivo imaging
• Introduced via tail vein injection, can be imaged for up to 3 hours after injection
• Available in four colors—565 nm, 655 nm, 705 nm, or 800 nm emission
Read more about SAIVI and about applications for Qdot™ nanocrystals.
For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use.
Need a different emission spectrum or longer tracking? View our other mammalian cell tracking products.
Key Attributes:
• Qtracker™ 705 label has Ex/Em (405-665/705) nm
• Designed for small animal in vivo imaging
• Introduced via tail vein injection, can be imaged for up to 3 hours after injection
• Available in four colors—565 nm, 655 nm, 705 nm, or 800 nm emission
Read more about SAIVI and about applications for Qdot™ nanocrystals.
For Research Use Only. Not intended for any animal or human therapeutic or diagnostic use.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Concentration2 μM
Dye TypeQdot Nanocrystals
Product LineQTRACKER, Qdot
Quantity200 μL
Reagent TypeVascular Imaging Reagents
Shipping ConditionRoom Temperature
TechniqueIn Vivo Imaging
Product TypeVascular Label
Unit SizeEach
Contents & Storage
Contains 200 μl Qtracker™ non-targeted quantum dots (2 μM solution in 50 mM borate buffer, pH 8.3). Store at 2–6°C. Do not freeze. Stable for at least 6 months.
Frequently asked questions (FAQs)
When I label with Qtracker cell labeling reagents, I get a punctate label pattern. How do I make it more uniform?
How long after injection should I start imaging my mouse?
What happens to unconjugated dye in the mouse after small animal in vivo imaging?
What amount of Qtracker non-targeted reagent should I inject to image vasculature?
I want to track my cells with a nucleic acid stain, like DAPI or Hoechst dye. Do you recommend this?
Citations & References (17)
Citations & References
Abstract
Noninvasive imaging of quantum dots in mice.
Journal:Bioconjug Chem
PubMed ID:14733586
'Quantum dots having four different surface coatings were tested for use in in vivo imaging. Localization was successfully monitored by fluorescence imaging of living animals, by necropsy, by frozen tissue sections for optical microscopy, and by electron microscopy, on scales ranging from centimeters to nanometers, using only quantum dots for
In vivo imaging of quantum dots.
Journal:Methods Mol Biol
PubMed ID:19488714
'Noninvasive whole-body near-infrared fluorescence imaging is now acknowledged as a powerful method for the molecular mapping of biological events in live small animals such as mouse models. With outstanding optical properties such as high fluorescence quantum yields and low photobleaching rates, quantum dots (QDs) are labels of choice in the
Imaging takes a quantum leap.
Journal:Physiology (Bethesda)
PubMed ID:15546848
Semiconducting nanocrystals, or quantum dots (QDs), have emerged as a new tool in physiological imaging, combining high brilliance, photostability, broad excitation but very narrow emission spectra, and surface chemistry compatible with biomolecular conjugation. In this review, we demonstrate the power of QDs in diverse applications, including long-term in vivo fluorescence
In vivo excitation of nanoparticles using luminescent bacteria.
Journal:Proc Natl Acad Sci U S A
PubMed ID:22615349
The lux operon derived from Photorhabdus luminescens incorporated into bacterial genomes, elicits the production of biological chemiluminescence typically centered on 490 nm. The light-producing bacteria are widely used for in vivo bioluminescence imaging. However, in living samples, a common difficulty is the presence of blue-green absorbers such as hemoglobin. Here we
Lymph node B lymphocyte trafficking is constrained by anatomy and highly dependent upon chemoattractant desensitization.
Journal:Blood
PubMed ID:22039261
B lymphocyte recirculation through lymph nodes (LNs) requires crossing endothelial barriers and chemoattractant-triggered cell migration. Here we show how LN anatomy and chemoattractant receptor signaling organize B lymphocyte LN trafficking. Blood-borne B cells predominately used CCR7 signaling to adhere to high endothelial venules (HEVs). New B cell emigrants slowly transited