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Ä«Å×°í¸® Enzymes & Inhibitors
CAT.NO LGP-45-007
PRODUCT PreScission Protease(PPase)
SIZE 100IU, 250IU
PRICE KRW 310,000, 495,000
.
Technical Parameters
Synonyms 3C protease, Picornain 3C, PSP
Source Escherichia coli.
Description PreScission Protease is a fusion protein of glutathione S-transferase (GST) and human rhinovirus (HRV) type 14 3C protease. The protease specifically recognizes a subset of sequences which include the core amino acid sequence Leu-Phe-Gln/Gly-Pro cleaving between the Gln and Gly residues. Substrate recognition and cleavage are likely to be dependent not only upon primary structural signals, but also upon the secondary and tertiary structures of the fusion protein as well.
Quantity 100IU/250IU
Unit Definition One unit is defined as the amount of enzyme needed to cleave 100 ¥ìg of fusion protein in 16 hours to 90 % completion at 5 ¡ÆC in a buffer containing 50 mM Tris-HCl, pH 7.0, 150 mM NaCl, 1 mM EDTA, and 1 mM DTT.
Physical Appearance Sterile colorless liquid.
Cleavage Buffer 50 mM Tris-HCl, pH 7.0 (at 25¡ÆC), 150 mM NaCl, 1 mM EDTA, 1 mM dithiothreitol. Chill to 5 ¡ÆC prior to use.
Recommended Conditions for Cleavage of a Fusion Protein During cleavage reactions, it is recommended that samples be removed at various time points and analyzed by SDS-PAGE to estimate the yield, purity, and extent of digestion. The amount of PreScission Protease, temperature and length of incubation required for complete digestion of a given GST fusion partner may vary depending on the fusion partner. Optimal conditions for each fusion should be determined in pilot experiments. Digestion may be improved by adding TritonTM X-100, TweenTM 20 or NonidetTM P40 to a concentration of 0.01 %. Concentrations of these detergents up to 1 % do not inhibit PreScission Protease.
Stability & Storage Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
- 6 months from date of receipt, -20 to -70 ¡ÆC as supplied.
- 3 months, -20 to -70 ¡ÆC under sterile conditions after opening.
Usage This material is offered by Korea Lugen Sci for research, laboratory or further evaluation purposes. NOT FOR HUMAN USE
SDS-PAGE
Reference 1. Werner G, Rosenwirth B, Bauer E, et al. 1986. J Virol, 57: 1084-93.
2. Libby RT, Cosman D, Cooney MK, et al. 1988. Biochemistry, 27: 6262-8.
3. Aschauer B, Werner G, McCray J, et al. 1991. Virology, 184: 587-94.
4. Leong LE, Walker PA, Porter AG. 1993. J Biol Chem, 268: 25735-9.
Background PreScission protease is a cysteine protease derived from human rhinovirus – HRV3C Protease. rPP is a fusion protein of glutathione S-transferase (GST) and human rhinovirus (HRV) type 14 3C protease. It specifically recognizes the amino acid sequences which include the core site of Leu-Phe-Gln-Gly-Pro and cleaves between the Gln and Gly residues. Substrate recognition and cleavage are likely to be dependent not only upon primary structural signals, but also upon the super structures of the fusion protein. rPP works most effective at 4¡É and can digest substrates at room temperature as well.

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