Search
Citations & References (13)
Invitrogen™
SNARF™-1 Carboxylic Acid, Acetate, Succinimidyl Ester - Special Packaging
Permits simultaneous long-term tracing of mixed-cell populations using different fluorescent colors
| Catalog Number | Quantity |
|---|---|
| S22801 | 10 x 50 μg |
Catalog number S22801
Price (EUR)
914,00
Each
Quantity:
10 x 50 μg
Price (EUR)
914,00
Each
To permit simultaneous long-term tracing of mixed-cell populations using different fluorescent colors, we have developed a probe whose applications should be similar to those of CFDA SE (commonly called CFSE). Cells labeled with our SNARF-1 carboxylic acid, acetate, succinimidyl ester have orange-red fluorescence that can be easily distinguished from that of cells loaded with green-fluorescent tracers such as CFDA SE.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodFluorescence
Dye TypeFluorescent Dye-Based
IndicatorpH Indicator
Quantity10 x 50 μg
Shipping ConditionRoom Temperature
For Use With (Application)Cell Tracing
For Use With (Equipment)Fluorescence Microscope, Flow Cytometer, Microplate Reader
Product LineSNARF
Product TypeCarboxylic Acid Acetate Succinimidyl Ester
Unit SizeEach
Contents & Storage
Store in freezer -5°C to -30°C.
Citations & References (13)
Citations & References
Abstract
Immunological effects of transgenic constitutive expression of the type 1 sphingosine 1-phosphate receptor by mouse lymphocytes.
Journal:J Immunol
PubMed ID:15699128
'The type 1 sphingosine 1-phosphate (S1P) G protein-coupled receptor (S1P1) normally transduces S1P effects on lymph node (LN) egress and tissue migration of naive lymphocytes. We now show that persistent expression of S1P1 by lymphocytes of S1P1-transgenic (Tg) mice suppresses delayed-type hypersensitivity and results in production of significantly more IgE
Discrepancy in measuring CD4 expression on T-lymphocytes using fluorescein conjugates in comparison with unimolar CD4-phycoerythrin conjugates.
Journal:Cytometry B Clin Cytom
PubMed ID:17474131
'BACKGROUND: Numerous methods for quantitative fluorescence calibration (QFC) have been developed to quantify receptor expression on lymphocytes. However, the results from the use of these different QFC methods vary considerably in the literature. To better identify the causes of these discrepancies, we measured CD4 expression using FITC and phycoerythrin (PE)
Tracking cell proliferation using the far red fluorescent dye SNARF-1.
Journal:Cytometry B Clin Cytom
PubMed ID:17397063
BACKGROUND: The [(3)H]thymidine incorporation assay and staining of living cells with fluorescent dyes like carboxyfluorescein diacetate, succinimidyl ester (CFSE) have evolved as valuable methods for studying T cell responses. To assess proliferation of cells already labeled by FITC, CFSE, GFP, or other
Dynamics of thymocyte-stromal cell interactions visualized by two-photon microscopy.
Journal:Science
PubMed ID:12052962
Thymocytes are selected to mature according to their ability to interact with self major histocompatibility complex (MHC)-peptide complexes displayed on the thymic stroma. Using two-photon microscopy, we performed real-time analysis of the cellular contacts made by developing thymocytes undergoing positive selection in a three-dimensional thymic organ culture. A large fraction
The relationship between Na(+)/H(+) exchanger expression and tyrosinase activity in human melanocytes.
Journal:Exp Cell Res
PubMed ID:15265699
The activity of melanosome-associated tyrosinase in human melanocytes differs based on racial skin type. In melanocytes from Black skin, tyrosinase activity is high while in White melanocytes the activity of the enzyme is low. Recent studies suggest that low tyrosinase activity in White melanocytes may be due to an acidic