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MINCLARET

Sigma-Aldrich

CellVue® Claret Far Red Fluorescent Cell Linker Mini Kit for General Membrane Labeling

Distributed for Phanos Technologies

Sinónimos:

Far red membrane labeling kit

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About This Item

Código UNSPSC:
12352207
NACRES:
NA.32

envase

pkg of 1 kit

fabricante / nombre comercial

Distributed for Phanos Technologies

condiciones de almacenamiento

protect from light

técnicas

flow cytometry: suitable

fluorescencia

λex 655 nm; λem 675 nm (CellVue claret dye)

aplicaciones

cell analysis
detection

método de detección

fluorometric

Condiciones de envío

ambient

temp. de almacenamiento

room temp

Categorías relacionadas

Aplicación

CellVue Claret kit fluoresces in the far red and may be used for general cell membrane labeling including in vitro cell labeling, in vitro lymphocyte proliferation studies,† in vivo cytotoxicity assays,† and also as a second color for monitoring cell-cell membrane transfer.†
CellVue® Claret Far Red Fluorescent Cell Linker Mini Kit for General Membrane Labeling has been used:
  • to label monocyte-derived macrophages (MDMs) for antibody-dependent cellular phagocytosis assay
  • in labeling of Jurkat cells after the induction of apoptosi
  • in labeling of cells in mice for assaying the retention of tumor cells in lung

Acciones bioquímicas o fisiológicas

The CellVue Claret Fluorescent Cell Linker kit uses a proprietary membrane labeling technology to stably incorporate a far red fluorescent dye with long aliphatic tails (CellVue Claret) into lipid regions of the cell membrane.†

Envase

This kit provides enough dye for up to 25 samples of 20 million cells each and enough diluent for up to 5 samples of 20 million cells each, when using a 2 mL final staining volume containing a final concentration of 2 x 10-6 M of PKH26 dye. Users must determine the optimal dye and cell concentrations from their cell type(s) and experimental purposes.

Ligadura / enlace

For additional technical details on Fluorescent Cell Linker Dyes including a comprehensive bibliography, please visit PKH and CellVue®; Claret Fluorescent Cell Linker Dyes.

Información legal

Distributed for Phanos Technologies, Inc.
Patent Information
CellVue is a registered trademark of Phanos Technologies

Pictogramas

FlameExclamation mark
GHS02,GHS07

Palabra de señalización

Danger

Frases de peligro

H225,H319

Clasificaciones de peligro

Eye Irrit. 2 - Flam. Liq. 2

Clase de riesgo para el agua (WGK)

WGK 1

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
MKCS3794
MKCL7230
MKCF6589
MKCF1396
MKCD3257

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Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

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The detergent-soluble cytoplasmic pool of survivin suppresses anoikis and its expression is associated with metastatic disease of human colon cancer
Hori M, et al.
Testing, 8(2), e55710-e55710 (2013)
Sudjit Luanpitpong et al.
Environmental science & technology, 48(21), 12912-12919 (2014-10-28)
Epidemiological studies suggest that living near mountaintop coal mining (MTM) activities is one of the contributing factors for high lung cancer incidence. The purpose of this study was to investigate the long-term carcinogenic potential of MTM particulate matter (PMMTM) exposure
Jun Sugimoto et al.
International journal of molecular sciences, 22(19) (2021-10-14)
Proper placental development relies on tightly regulated trophoblast differentiation and interaction with maternal cells. Human endogenous retroviruses (HERVs) play an integral role in modulating cell fusion events in the trophoblast cells of the developing placenta. Syncytin-1 (ERVW-1) and its receptor
Justin L Spinner et al.
Journal of leukocyte biology, 95(3), 389-398 (2013-11-15)
Yersinia pestis, the bacterial agent of plague, is transmitted by fleas. The bite of an infected flea deposits Y. pestis into the dermis and triggers recruitment of innate immune cells, including phagocytic PMNs. Y. pestis can subvert this PMN response
Robert Moore et al.
Biology open, 3(2), 121-128 (2014-01-15)
The primitive endoderm epithelial structure in mouse blastocysts forms following cell differentiation and subsequent sorting, and this two-step process can be reproduced in vitro using an embryoid body model. We found that in the chimeric embryoid bodies consisting of paired
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