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Merck

P6649

Millipore

Protein A–Sepharose 6 MB

aqueous ethanol suspension

Synonym(e):

Protein-A-Agarose-Makrobeads

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About This Item

MDL-Nummer:
UNSPSC-Code:
41106500
NACRES:
NA.56

Form

aqueous ethanol suspension

Qualitätsniveau

Kennzeichnungsgrad

~1 mg per mL

Matrixaktivierung

cyanogen bromide

Matrixanbindung

amino

Matrix-Spacer

1 atom

Kapazität

~6 mg/mL binding capacity (human IgG)

Lagertemp.

2-8°C

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Allgemeine Beschreibung

P6649-10ml′s updated product number is GE17-0469-01

Anwendung

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 6MB has been used in immunoprecipitation.

Physikalische Form

Suspension in 20% Ethanol

Rechtliche Hinweise

Sepharose is a trademark of Cytiva

Piktogramme

Flame

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Flam. Liq. 3

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

100.4 °F

Flammpunkt (°C)

38 °C


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G V Hillyer et al.
The American journal of tropical medicine and hygiene, 38(3), 547-552 (1988-05-01)
Total RNA containing messenger RNA has been isolated from adult Fasciola hepatica and translated in vitro using the rabbit reticulocyte lysate system. L-[35S]-methionine labeled translation products have been immunoprecipitated with sera collected from rabbits infected with F. hepatica, rabbits immunized
Sundar Rajan Selvaraj et al.
Molecular biology of the cell, 19(12), 5579-5592 (2008-09-26)
Retinol-binding protein (RBP) is secreted out of the cell in its ligand-bound holo-form. The apo-form of RBP is selectively retained within the endoplasmic reticulum (ER) by a mechanism that remains unknown. Using isolated microsomal system, we have recapitulated the biogenesis
L F Wang et al.
Gene, 169(1), 53-58 (1996-02-22)
Epitope tagging (Eta) is becoming an increasingly useful technique in molecular biology and biotechnology for the detection, characterisation and purification of recombinant proteins (re-proteins). Here we describe a novel Eta system composed of two different monoclonal antibodies (mAb; D11 and
Gaurav Dugar et al.
Molecular cell, 69(5), 893-905 (2018-03-03)
Cas9 nucleases naturally utilize CRISPR RNAs (crRNAs) to silence foreign double-stranded DNA. While recent work has shown that some Cas9 nucleases can also target RNA, RNA recognition has required nuclease modifications or accessory factors. Here, we show that the Campylobacter
A J Williams et al.
Diabetes care, 24(3), 504-509 (2001-04-06)
To determine the extent of celiac autoimmunity in type 1 diabetic patients and the overlap between islet and celiac autoimmunity in their nondiabetic relatives. IgA antibodies to tissue transglutaminase were determined in serum taken from 433 type 1 diabetic patients

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