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P9424

Millipore

ProteinA-Sepharose™ 4, Fast Flow from Staphylococcus aureus

aqueous ethanol suspension

Sinonimo/i:

Protein A–Agarose

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About This Item

Numero MDL:
MFCD00165563
Codice UNSPSC:
41106500
NACRES:
NA.56

Origine biologica

Staphylococcus aureus

Livello qualitativo

100

Forma fisica

aqueous ethanol suspension

Classi chimiche degli analiti

proteins (Immunoglobulins of various mammalian species)

Grado di funzionalizzazione

~6 mg per mL

tecniche

affinity chromatography: suitable

Matrice

Sepharose 4B Fast Flow

Attivazione matrice

cyanogen bromide

Gruppi immobilizzati alla matrice

amino

Braccio spaziatore

1 atom

Capacità

≥30 mg/mL binding capacity (human IgG)

Temperatura di conservazione

2-8°C

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Categorie correlate

Descrizione generale

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.

Applicazioni

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

Stato fisico

Suspension in 20% ethanol

Note legali

Sepharose is a trademark of Cytiva

Pittogrammi

Flame
GHS02

Avvertenze

Warning

Indicazioni di pericolo

H226

Classi di pericolo

Flam. Liq. 3

Classe di pericolosità dell'acqua (WGK)

WGK 3

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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The Journal of biological chemistry, 270(1), 254-262 (1995-01-06)
During each cell cycle, the nucleus of higher eukaryotes undergoes a dramatic assembly and disassembly. These events can be faithfully reproduced in vitro using cell-free extracts derived from Xenopus eggs. Such extracts contain three major N-acetylglucosaminylated proteins, p200, p97, and
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European journal of immunology, 41(5), 1288-1297 (2011-04-07)
T-cell receptors (TCRs) can be genetically modified to improve gene-engineered T-cell responses, a strategy considered critical for the success of clinical TCR gene therapy to treat cancers. TCR:ζ, which is a heterodimer of TCRα and β chains each coupled to
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The Journal of biological chemistry, 276(35), 33220-33232 (2001-06-30)
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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.
Proceedings of the National Academy of Sciences of the United States of America, 90(20), 9422-9426 (1993-10-15)
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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