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Merck

D4513

Sigma-Aldrich

Desoxirribonucleasa I from bovine pancreas

Type II-S, lyophilized powder, Protein ≥80 %, ≥2,000 units/mg protein

Sinónimos:

ADNasa I, Desoxirribonucleato 5′-oligonucleótido-hidrolasa

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About This Item

Número de CAS:
Comisión internacional de enzimas:
Número CE:
Número MDL:
Código UNSPSC:
12352204
NACRES:
NA.54

origen biológico

bovine pancreas

Nivel de calidad

esterilidad

sterile-filtered

tpo

Type II-S

Formulario

lyophilized powder

actividad específica

≥2,000 units/mg protein

mol peso

~31 kDa

purificado por

chromatography

composición

Protein, ≥80%

envase

vial of ≥10.0 mg protein

técnicas

DNA purification: suitable

impurezas

endotoxin, tested

solubilidad

0.15 M NaCl: soluble 5.0 mg/mL, clear(lit.)

idoneidad

suitable for molecular biology

aplicaciones

diagnostic assay manufacturing
diagnostic assay manufacturing

actividad extraña

Chymotrypsin ≤0.01%
Protease ≤0.005%
RNase ≤0.01%

temp. de almacenamiento

−20°C

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Aplicación

Utilizado para eliminación del ADN de las muestras proteicas.
DNAse I from Sigma has been compared with human urine-derived interleukin 1 inhibitor for the ability to hydrolyze [14C]DNA [14C]DNA. It has also been used to cleave a 139 base pair Hind III/Nci I restriction fragment to investigate the stability of the enzyme for use in footprinting experiments. DNase I is widely used as a footprinting agent for studying drug and protein binding to DNA.
Deoxyribonuclease I from bovine pancreas has been used in a study to investigate a new approach to obtaining high-activity RNase, DNase, cholesterolesterase, and trypsin from cattle pancreas. Deoxyribonuclease I from bovine pancreas has also been used in a study to investigate the isolation and further characterization of carp liver DNase.

Acciones bioquímicas o fisiológicas

DNase I is an endonuclease that acts on phosphodiester bonds adjacent to pyrimidines to produce polynucleotides with terminal 5′-phosphates. In the presence of Mg2+, DNAse I cleaves each strand of DNA independently and the cleavage sites are random. Both DNA strands are cleaved at approximately the same site in the presence of Mn2+. The pH optimum lies between 7 and 8. Divalent cations such as Mn2+, Ca2+, Co2+, and Zn2+ are activators of the enzyme. A concentration of 5 mM Ca2+ stabilizes the enzyme against proteolytic digestion. DNAse I from bovine pancreas consists of four chromatographically distinguishable components, A, B, C, and D, with their molar ratios being 4:1:1 respectively. Only minor amounts of D are found. 2-Mercaptoethanol, chelators, sodium dodecyl sulfate (SDS) and actin are known to inhibit the enzyme activity.

Definición de unidad

One Kunitz unit will produce a ΔA260 of 0.001 per min per mL at pH 5.0 at 25 °C, using DNA, Type I or III as substrate. (1 unit = 1 Kunitz unit)

Forma física

Lyophilized powder containing calcium chloride

Nota de preparación

The enzyme powder may be reconstituted in water or any buffer at pH 4.0-9.0, except phosphate buffer. Calcium chelators should be avoided. 10 mg/mL solution of DNAse I in 0.15 M NaCl may lose <10% of its activity when stored for a week in aliquots at −20 °C. The same solutions stored in aliquots at 2-8 °C can lose approximately 20% activity. It remains active for up to five hours at 60 °C between pH 5 and 7, and loses activity in <10 minutes at 68 °C. It loses activity at the rate of 6%/hour in acetate buffer (pH 5.0) and tris buffer ((pH 7.2) at 1 mg/mL concentration.

Nota de análisis

Protein determined by biuret.

Pictogramas

Health hazard

Palabra de señalización

Danger

Frases de peligro

Consejos de prudencia

Clasificaciones de peligro

Resp. Sens. 1

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Certificados de análisis (COA)

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Visite la Librería de documentos

Enzymes of Molecular Biology
Weir, A. F.
Methods in Molecular Biology, 16 (1993)
Stability of DNase I in footprinting experiments.
B Ward et al.
Nucleic acids research, 16(17), 8724-8724 (1988-09-12)
D L Rosenstreich et al.
The Journal of experimental medicine, 168(5), 1767-1779 (1988-11-01)
We have previously reported that the urine of febrile humans contained large quantities of an inhibitor of IL-1-induced murine thymocyte proliferation that was a glycoprotein between 30 and 40 kD in size. In the present study this factor has been
Daniel Engelbertsen et al.
Scientific reports, 9(1), 10608-10608 (2019-07-25)
CD47, also known as integrin-associated protein (IAP), is a transmembrane protein with multiple biological functions including regulation of efferocytosis and leukocyte trafficking. In this study we investigated the effect of CD47-deficiency on atherosclerosis using a model of adeno-associated virus (AAV)-induced
T Liao
The Journal of biological chemistry, 250(10), 3831-3836 (1975-05-25)
In the course of experiments on the role of the COOH-terminal residues in pancreatic deoxyribonuclease, we undertook to ascertain whether the presence of sodium dodecyl sulfate would render the normally unavailable terminus susceptible to hydrolysis by carboxypeptidase A. When DNase

Protocolos

To standardize a procedure for the enzymatic assay of Deoxyribonuclease I.

To standardize a procedure for the enzymatic assay of Deoxyribonuclease I.

To standardize a procedure for the enzymatic assay of Deoxyribonuclease I.

To standardize a procedure for the enzymatic assay of Deoxyribonuclease I.

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