Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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I293856-100U | 100U | Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding. | $426.90 |
Specifications & Purity | 95% by SDS-PAGE |
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Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | EnzymoPure™ |
Product Description | Description General description Molecular Weight: 71 kDa (homodimer consisting of two equal subunits of molecular weight 32-35 kDa) Extinction Coefficient: E1% = 14.5 (280 nm) pI: 4.75 This ubiquitous enzyme serves to drive metabolic reactions that produce pyrophosphate, since these reactions typically have equilibrium constants near unity. The catalytic mechanism has been described in the literature. Inorganic pyrophosphatase is a metalloprotease that requires Mg2+ for maximal activity. Although the hydrolysis of inorganic pyrophosphate is specific in the presence of Mg2+, both ADP and ATP can be hydrolyzed if zinc is present. Application Inorganic pyrophosphatase (PPase) is a ubiquitous enzyme catalyzing the reaction PPi + H2O → 2Pi. It plays an important role in protein, RNA, and DNA synthesis. Pyrophosphatase has been used: as a component of the reaction buffer used in aminoacylation assay to quantify incorporation of 3HL-methionine into tRNA. as a component of PCR mixture Pyrophosphatase has been used: as a component of the reaction buffer used in aminoacylation assay to quantify incorporation of 3HL-methionine into tRNA. as a component of PCR mixture. |
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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Canonical SMILES | CC1=C2C(N(CCC2=NN1)C(=O)C=CC3=C(C=CC(=C3F)Cl)N4C=NN=N4)C(=O)CC5=CC=C(C=C5)C(=O)C.CC1=C2C(N(CCC2=NN1)C(=O)C=CC3=C(C=CC(=C3F)Cl)N4C=NN=N4)C(=O)CC5=CC=C(C=C5)C(=O)OC(C)(C)C |
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Isomeric SMILES | CC1=C2C(N(CCC2=NN1)C(=O)C=CC3=C(C=CC(=C3F)Cl)N4C=NN=N4)C(=O)CC5=CC=C(C=C5)C(=O)C.CC1=C2C(N(CCC2=NN1)C(=O)C=CC3=C(C=CC(=C3F)Cl)N4C=NN=N4)C(=O)CC5=CC=C(C=C5)C(=O)OC(C)(C)C |
PubChem CID | 168266391 |
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1. Rao Honghong, Li Jianying, Luo Mingyue, Zhang Kehui, Gou Hao, Liu Haixia, Xue Zhonghua. (2022) A label-free and modification-free ratiometric electrochemical strategy for enhanced natural enzyme detection using a bare electrode and nanozymes system. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 414 (9): (2991-3003). [PMID:35106612] |
1. Rao Honghong, Li Jianying, Luo Mingyue, Zhang Kehui, Gou Hao, Liu Haixia, Xue Zhonghua. (2022) A label-free and modification-free ratiometric electrochemical strategy for enhanced natural enzyme detection using a bare electrode and nanozymes system. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 414 (9): (2991-3003). [PMID:35106612] |