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About This Item
conjugate
agarose conjugate
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
M2, monoclonal
form
buffered aqueous glycerol solution
analyte chemical class(es)
proteins
technique(s)
affinity chromatography: suitable, immunoprecipitation (IP): suitable
matrix
(4% agarose bead; 45-165μm bead size)
isotype
IgG1
capacity
>0.6 mg/mL, resin binding capacity (FLAG-BAP)
shipped in
wet ice
storage temp.
−20°C
Quality Level
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Related Categories
Application
Learn more product details in our FLAG® application portal.
Disclaimer
General description
Elution - FLAG® peptide, Glycine, pH 3.5, 3x FLAG® peptide
Immunogen
Physical form
Legal Information
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Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
A2220-BULK: + A2220-2X25ML: + A2220-1ML: + A2220-4X25ML: + A2220-5ML: + A2220-10ML: + A2220-1ML-KC: + A2220PROC: + A2220-VAR: + A2220-25ML:
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Articles
The FLAG® Expression System is a proven method to express, purify and detect recombinant fusion proteins. Sigma®, the proven provider of FLAG®, now offers a magnetic bead for immunoprecipitation, protein purification, and the study of protein-protein interactions. The ANTI-FLAG® M2 Magnetic Bead is composed of murine derived, anti-FLAG® M2 monoclonal antibody attached to superparamagnetic iron impregated 4% agarose beads, with an average diameter of 50 µm. The M2 antibody is capable of binding to fusion proteins containing a FLAG peptide sequence at the N-terminus, Met-N-terminus, or C-terminus locations in mammalian, bacterial, and plant extracts.
Protocols
Protocol for immunoprecipitation (IP) of FLAG fusion proteins using M2 monoclonal antibody 4% agarose affinity gels
M2モノクローナル抗体4%アガロースアフィニティーゲルを使用したFLAG®融合タンパク質の免疫沈降(IP)のためのプロトコル
Related Content
イオン交換、サイズ排除、タンパク質アフィニティークロマトグラフィーなどの方法を用いた組換えタンパク質精製のためのタンパク質精製技術、試薬、プロトコル。
Protein purification techniques, reagents, and protocols for purifying recombinant proteins using methods including, ion-exchange, size-exclusion, and protein affinity chromatography.
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