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76508

Sigma-Aldrich

Atto 647N Protein Labeling Kit

BioReagent, suitable for fluorescence

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About This Item

Código UNSPSC:
12352108
NACRES:
NA.32

Línea del producto

BioReagent

Nivel de calidad

100

fabricante / nombre comercial

ATTO-TEC GmbH

fluorescencia

λex 647 nm; λem 661 nm in 0.1 M phosphate buffer, pH 7.0 (recommended)

idoneidad

suitable for fluorescence

temp. de almacenamiento

2-8°C

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Descripción general

This kit contains sufficient amounts of reactive dye, buffers and protein purification sets for performing five labeling reactions (1 mg protein each) and for the subsequent purification of the labeled protein.

Información legal

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

Código de clase de almacenamiento

10 - Combustible liquids

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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Certificados de análisis (COA)

Lot/Batch Number
BCCL9682
BCCK6675
BCCK2483
BCCJ0360
BCCF4065

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

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Bryant L Doss et al.
Proceedings of the National Academy of Sciences of the United States of America, 117(23), 12817-12825 (2020-05-24)
Morphogenesis, tumor formation, and wound healing are regulated by tissue rigidity. Focal adhesion behavior is locally regulated by stiffness; however, how cells globally adapt, detect, and respond to rigidity remains unknown. Here, we studied the interplay between the rheological properties
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The role of microglia cells in Alzheimer's disease (AD) is well recognized, however their molecular and functional diversity remain unclear. Here, we isolated amyloid plaque-containing (using labelling with methoxy-XO4, XO4+) and non-containing (XO4-) microglia from an AD mouse model. Transcriptomics
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Bio-protocol, 11(2), e3899-e3899 (2021-03-19)
β-hemoglobinopathies are severe genetic disorders characterized either by the abnormal synthesis of the adult β-globin chains of the hemoglobin (Hb) tetramer (βS-globin chains) in sickle cell disease (SCD) or by the reduced β-globin production in β-thalassemia. The identification and quantification
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BMC Cell Biology, 10(1), 88-88 (2009)
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