P9424
Proteína A – Agarosa
aqueous ethanol suspension
Sinónimos:
Protein A–Agarose
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About This Item
Productos recomendados
origen biológico
Staphylococcus aureus
Formulario
aqueous ethanol suspension
clases químicas de analitos
proteins (Immunoglobulins of various mammalian species)
Extensión del etiquetado
~6 mg per mL
técnicas
affinity chromatography: suitable
Matriz
Sepharose 4B Fast Flow
activación de la matriz
cyanogen bromide
unión a la matriz
amino
espaciador de matriz
1 atom
capacidad
≥30 mg/mL binding capacity (human IgG)
temp. de almacenamiento
2-8°C
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Descripción general
Protein A-Sepharose™ has been used to develop strategies for investigating protein interactions, to improve the detection of celiac disease, and to study diabetes in children.
Aplicación
Protein A-Sepharose is used for affinity chromatography, antibody purification and characterization, immunoaffinity matrices, protein chromatography, protein A, G and L resins, and recombinant protein expression and analysis. Protein A-Sepharose™ has been used to develop strategies for investigating protein interactions, to improve the detection of celiac disease, and to study diabetes in children.
Protein A-Sepharose™ Fast Flow from Staphylococcus aureus has been used:
- in co-immunoprecipitation assay
- in immunodepletion
- to purify IgG from human serum and plasma
Forma física
Suspension in 20% ethanol
Información legal
Sepharose is a trademark of Cytiva
Palabra de señalización
Warning
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Flam. Liq. 3
Clase de riesgo para el agua (WGK)
WGK 3
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Chromatin immunoprecipitation (ChIP) combined with high-throughput sequencing (ChIP-seq) has become the gold standard for whole-genome mapping of protein-DNA interactions. However, conventional ChIP protocols necessitate the use of large numbers of cells, and library preparation steps associated with current high-throughput sequencing
H Sternlicht et al.
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A role in folding newly translated cytoskeletal proteins in the cytosol of eukaryotes has been proposed for t-complex polypeptide 1 (TCP1). In this study, we investigated tubulin and actin biogenesis in Chinese hamster ovary (CHO) cells. When extracts of pulse-labeled
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