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The KspAI (HpaI) restriction enzyme recognizes GTT^AAC sites and cuts best at 37°C in B buffer (Isoschizomers: HpaI).
Cut at W^GTACW sites with TatI restriction enzyme, which performs best at 65°C in Tango buffer.
Cut at G^GYRCC sites with BshNI (BanI) restriction enzyme, which performs best at 37°C in O buffer (Isoschizomers: AccB1I, BanI, BspT107I).
The PagI (BspHI) restriction enzyme recognizes T^CATGA sites and cuts best at 37°C in O buffer (Isoschizomers: BspHI, CciI, RcaI).
Cell permeant
A recombinant fragment of ULP1 (Ubl-specific protease 1) from Saccharomyces cerevisiae
Purified from bovine pancreas
Purified and tested for nondetectable levels of RNase contamination
Suitable for use with M13/phagemid hosts for the production of ssDNA from vectors containing an f1or f1-like origin of replication
Self-coating synthetic surface for stem cells
Widely used chromogenic substrate for β-galactosidase
Cleavage produces blue-fluorescence
Continuously assay acid phosphatases at low pH
For the hydrolysis product, resorufin
Novex™ AP Chromogenic Substrate (BCIP/ NBT)