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Merck
CN

D8764

Sigma-Aldrich

脱氧核糖核酸酶II 来源于牛脾脏

Type V, essentially salt-free, lyophilized powder, ≥1,000 units/mg protein

别名:

DNase II, 脱氧核苷酸酶 3′-寡核苷酸脱氢酶

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About This Item

CAS号:
EC 号:
MDL编号:
UNSPSC代码:
12352204
NACRES:
NA.54

生物来源

bovine spleen

质量水平

类型

Type V

形式

essentially salt-free, lyophilized powder

比活

≥1,000 units/mg protein

分子量

38 kDa

浓度

≥50% protein

技术

DNA extraction: suitable
tissue culture: suitable

适用性

suitable for molecular biology

应用

cell analysis

异质活性

RNase ≤0.1%

储存温度

−20°C

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应用

牛脾脱氧核糖核酸酶Ⅱ已用于:
  • 作为从结肠样品分离免疫细胞的消化混合液组分
  • 消化视网膜外植体以制备单细胞悬液
  • 分离人结肠组织的基质细胞
  • 作为从大鼠心脏制备胚胎心肌细胞的解离培养基组分

生化/生理作用

脱氧核糖核酸酶II,也称为酸性DNA酶,可水解天然和变性DNA中的脱氧核糖核苷酸连接键,产生带有3′-磷酸的产物。体外最佳pH范围是4.5-5.0。它还可在pH 5.6-5.9下作用于对硝基苯基磷酸二酯。分子量约为38,000 Da。

单位定义

在 pH 4.6 25℃条件下,一个Kunitz单位可每分钟在每毫升内产生0.001的ΔA260;[Mg2+] = 0.83 mM

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

动植物源性产品

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Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 114(2), 119-128 (1994-02-01)
Deoxyribonucleases from eggs and the liver of Xenopus laevis were partially purified by DEAE-cellulose and heparin-Sepharose affinity column chromatographies. The fractions having egg and liver DNase activities were eluted on high performance liquid chromatography through TSK gel G3000SW at the
Dopamine D2 receptor stimulation differentially affects voltage-activated calcium channels in rat pituitary melanotropic cells.
Keja J A, et al.
The Journal of Physiology, 450(1), 409-435 (1992)
S Ingebrandt et al.
Biosensors & bioelectronics, 16(7-8), 565-570 (2001-09-07)
An extracellular recording system has been designed for the detection of electrical cell signals using p-channel or n-channel field-effect transistor (FET) arrays with non-metallized gates. Signals from rat heart muscle cell were recorded by these devices and the results described
Therese Ostberg et al.
Arthritis and rheumatism, 62(10), 2963-2972 (2010-06-10)
High mobility group box chromosomal protein 1 (HMGB-1) is a DNA binding nuclear protein that can be released from dying cells and activated myeloid cells. Extracellularly, HMGB-1 promotes inflammation. Clinical and experimental studies demonstrate that HMGB-1 is a pathogenic factor
STUDIES ON ACID DEOXYRIBONUCLEASE. II. ISOLATION AND CHARACTERIZATION OF SPLEEN-ACID DEOXYRIBONUCLEASE.
G BERNARDI et al.
Biochemistry, 3, 1419-1426 (1964-10-01)

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