bsm-33133M-BF594

DATASHEET

Host: Mouse

Target Protein: TAP-Tag

Clonality: Monoclonal

Isotype: IgG

Source: Recombinant TAP-Tag

Purification: purified by Protein A.

Storage Buffer: Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Storage: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Background:

Tandem affinity purification (TAP) is a purification technique for studying proteinprotein interactions. It involves creating a fusion protein with a designed piece, the TAP tag, on the end. The original TAP method involves the fusion of the TAP tag to the C-terminus of the protein under study. The TAP tag consists of calmodulin binding peptide (CBP) from the N-terminal, followed by tobacco etch virus protease (TEV protease) cleavage site and Protein A, which binds tightly to IgG. The relative order of the modules of the tag is important because Protein A needs to be at the extreme end of the fusion protein so that the entire complex can be retrieved using an IgG matrix.

Conjugation: AbBy Fluor-594

Excitation/ Emission: 590nm/617nm

Size: 100ul

Concentration: Lot Dependent

Applications: WB(1:300-5000)
ELISA(1:500-1000)

Cross Reactive Species: Species independent

For research use only. Not intended for diagnostic or therapeutic use.