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Products:Tags & Cell Markers >> Epitope Tags >> Glu-Glu Tag
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Read our guarantee »Anti-Glu-Glu tag antibody [Glu-Glu] - Affinity Matrix
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Mouse monoclonal [Glu-Glu] to Glu-Glu tag - Affinity Matrix
This affinity Matrix can be used for immunopurification of Glu-Glu tagged fusion proteins from crude starting material.Binding: Tagged protein will bind to matrix in common physiologic buffers with pH in the range of 6.0-7.5, salt from 50-500 mM and in the presence of reasonable levels of detergent. Excess reducing agent should be avoided as the disulfide bridges holding antibody heavy and light chains may be compromised.Washing: After binding, washes with several bead volumes of buffer are recommended.Elution: Several options are available for elution. 1. SDS gel loading buffer may be applied directly to the beads in order to display all bound protein on a polyacrylamide gel/western. Note that gel loading buffer containing reducing agent will also release some antibody heavy and light chains (approx 25 and 50kD, respectively). 2. Competitive elution with epitope peptide. For epitope tag affinity matrices, prepare an elution buffer with epitope tag peptide at 400 ug/ml in 50 mM Tris-HCl (pH 7.5), 50 mM NaCl, 1 mM EDTA (pH 8.0). 3. Chemical elution. Elution by pH or chaotropic salts is also possible. For elution by pH, either 0.1 M glycine pH 2.8 or 40 mM diethyl-amine pH 11.0 may be used.
Synthetic peptide: CEEEEYMPME derived from the polyoma virus medium T antigen.
CEEEEYMPME
ab24587 is extremely specific and recognizes either six amino acid sequence, EYMPME, or EFMPME.
Liquid
Store at +4°C.
The slurry contains,
Preservative: 0.03% Thimerosal (merthiolate)
Constituents: PBS
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Protein G purified
This antibody was purified using protein-G chromatography and was subsequently immobilized onto a Sepharose(TM) Fast Flow matrix.
Monoclonal
Glu-Glu
IgG
Our Abpromise guarantee covers the use of ab24587 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
AP: Use at an assay dependent dilution. Note: The matrix may be re-used several times. To strip column after use, wash with several bead volumes 0.1 M glycine pH 2.8 followed immediately by PBS containing 0.3% thimerosol or 1mM azide as preservative.
IP: Use at an assay dependent dilution.
This product has been referenced in:
See 1 publication for this product
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