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Kinase/Phosphate

Product#: DC-Kinase-Phostphate

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Kinase/Phosphate

Product		Cat No.	Details	Size	Link
	Alkaline Phosphatase (Thermosensitive)	SB-G3400-1000U	Features: rapid dephosphorylation; Thermal instability Source: E. coli strain carrying tab5 alkaline phosphatase gene Inactivation or inhibition: heating at 80 ℃ for 2 min can fully inactivate alkaline phosphorase Purity and concentration: SDS-PAGE detection purity ≥ 95%, 5 u/ μL	1000 U
	Glucokinase, Thermostable	FNK-GLK-97-01	Highly stable and durable for long term use High reactivity at high temperature (70 - 100°C) Resistance to organic solvent is expected Special instruments to inhibit bacterial growth are not required Reaction speficity is much higher compared with chemical reaction Speed of reaction can be accelerated	1 ml
	Inorganic Pyrophosphatase (Yeast)	SB-G3460-100U	Source: Derived from Saccharomyces cerevisiae Purity and concentration: SDS-PAGE detection purity > 95%; endogenous nucleic acid residue < 1 pg/μL (qPCR detection); 1 U/μL Enzyme storage buffer: 20 mM Tris-HCl, 100 mM NaCl, 1 mM DTT, 0.1 mM EDTA, 50% Glycerol, pH 8.0	100 U
	Pyruvate Kinase HI1, Thermostable	FNK-PYK-75-01	Protein conc. 1.5 mg/ml Form 50 mM Tris-HCl (pH 7.5), 50 mM NaCl Activity 113 U/ml Substrate phosphoenolpyruvic acid Reaction product pyruvic acid Reaction temperature ~75℃ Reaction pH 5.0~8.0	1 ml
	Lamda Protein Phosphatase	FNK-02-300	Applications λ-PPase can be used to release phosphate groups from phosphorylated serine, threonine, tyrosine and histidine residues in proteins Form 400 U/ul λ-PPase in 50mM HEPES (pH 7.5), 100mM NaCl, 2mM dithiothreitol, 0.1 mM MnCl2, 0.1mM EDTA, 50% glycerol, 0.01% Brij 35 Purity Greater than 95% as determined by SDS-PAGE (CBB staining)	20000 units
	Lamda Protein Phosphatase	FNK-02-300-5		5x20000 units
	Pyruvate Kinase KS1, Thermostable	FNK-PYK-88-01	Protein conc. 4.9 mg/ml Form 50 mM Tris-HCl (pH 7.5), 50 mM NaCl Activity 145 U/ml Substrate phosphoenolpyruvic acid Reaction product pyruvic acid Reaction temperature ~85℃ Reaction pH 5.0~8.0	100 units
	T4 Polynucleotide Kinase	SB-G3458-500U	Source: Derived from T4 bacteriophage Purity and concentration: SDS-PAGE detection purity ≥ 95%; endogenous nucleic acid residue < 1 pg/μL (qPCR detection); 10 U/μL Inactivation: The enzyme can be inactivated by incubating at 65°C for 20 minutes Enzyme storage buffer: 10 mM Tris-HCl, 50 mM KCl, 1 mM DTT, 0.1 mM EDTA, 50% Glycerol, pH 7.4 10х Reaction buffer: 500 mM Tris-HCl, 100 mM MgCl₂ , 5 mM DTT, pH 7.6	500 U

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