Creatine Phosphokinase from rabbit muscle, Type I, salt-free, lyophilized powder, >=150 units/mg protein

Code: c3755-35ku D2-231

Not available outside of the UK & Ireland.

Analysis Note

Protein determined by biuret.

Application

Molecular Weight: ~81,000Creatine Phosphokinase is a dimer composed predominantly of the ...


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$375.55 EACH

Not available outside of the UK & Ireland.

Analysis Note

Protein determined by biuret.

Application

Molecular Weight: ~81,000Creatine Phosphokinase is a dimer composed predominantly of the skeletal muscle derived homodimer (MM). CK also exists as a heterodimer (MB) particularly in the myocardium. CK derived from brain tissue consists mainly of the brain source homodimer (BB). The amino acid sequences of the M chain and B chains are about 80% homologous. From the sequence, the molecular weight of the M chain is 43,112.E1%(280)= 8.76pH Optimum: pH 8.8-9.0 for the forward reaction and pH 6.0-7.0 for the reverse reaction.CK is a cellular enzyme with a wide tissue distribution. Its physiological role is associated with ATP generation for contractile or transport systems. Increased levels of CK are associated with myocardial infarction, muscular dystrophy, hyperthyroidism, pulmonary infarction and cerebrovascular disease. Variations in relative isozyme distribution can provide additional information in the diagnosis of these conditions. Substrates: Creatine, N-ethylglycocyamine and glyocyamine have been shown to act as substrates for CK. CK is very specific for ATP/ADP. Inhibitors: ADP is a strong inhibitor of the forward reaction competing with ATP. Divalent cations such as Ca2+ (Ki=4.5 mM), Zn2+ and Cu2+ inhibit CK by competing with Mg2+. Other inhibitors include acetate, acetylsalicylic acid, adenosine, p-aminosalicylic acid, AMP, benzoic acid, bicarbonate, bromide, chloride, p-Chloromercuribenzoic acid, ethylene oxide, 2,4-fluorodinitrobenzene, iodide, malonic acid, NAD, nitrate, phosphate, pyrophosphate, salicylic acid, sulfate, sulfite, thyroxine, trichloroacetate, L-triiodothyroxine, L-triiodothyronine, and tripolyphosphate.

The enzyme from Sigma has been used in the measurement of phosphocreatine in hippocampal neurons isolated from rat brains.

Caution

The use of 0.1% albumin in the reaction buffer is recommended to avoid inactivation due to dilution.

Packaging

500, 1000, 3500, 17500, 35000 units in poly bottle

Preparation Note

Produces a clear, colorless to light yellow solution at 5 mg/mL in 0.25 M glycyl-glycine, pH 7.4

Unit Definition

One unit will transfer 1.0 µmole of phosphate from phosphocreatine to ADP per min at pH 7.4 at 30 °C.

foreign activityLactic dehydrogenase, hexokinase, myokinase and pyruvate kinase ≤0.001%, ATPase ≤0.01%
formsalt-free, lyophilized powder
mol wt80-86.2 kDa
Quality Level200
shipped inwet ice
solubility0.25 M glycyl-glycine, pH 7.4: soluble 5.0 mg/mL, clear, colorless to slightly yellow
specific activity≥150 units/mg protein
storage temp.−20°C
typeType I
Code
Description
Unit Size
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Cas Number9001-15-4
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