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 t
Clonality:
Monoclonal
Concentration:
1ug/ul
Clone Designation:
[Mix-mA?]
Buffer:
Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Source:
Recombinant TAP-Tag
Purity:
Purified by Protein A.
Target:
TAP-Tag
Application Dilute:
WB(1:300-5000)
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