 |
北京西美杰科技有限公司
主營產品： 生物學檢測試劑盒,化學試劑,蛋白質氧化損傷,抗原抗體 |
16
聯系電話
18210960361
公司信息
- 聯系人：
- 西美杰
- 電話：
- 400-050-4006
- 手機：
- 18210960361
- 售后電話：
- 010-88597838
- 地址：
- 北京市海淀區金源時代商務中心B座10F
- 郵編：
- 100097
- 網址：
- www.xmjsci.com
[供應]A2760,0100 100 mg A2760,0500 500 mg A2760,1000 1 g-RNase A（核糖核酸酶A）
- 貨物所在地：
- 北京北京市
- 產地：
- 德國
- 更新時間：
- 2024-09-03 21:00:03
- 有效期：
- 2024年9月3日--2025年3月3日
- 已獲點擊：
- 421
【簡單介紹】RNase A
A2760,0100 100 mg
A2760,0500 500 mg
A2760,1000 1 g
A2760,0100 100 mg
A2760,0500 500 mg
A2760,1000 1 g
【詳細說明】
| Synonym | Ribonuclease A | |||
|---|---|---|---|---|
| delivery form | salt-free, freeze dried | |||
| origin | from bovine pancreas | |||
| M | ~13700 g/mol | |||
| CAS-No. | 9001-99-4 | |||
| HS-No. | 35079090 | |||
| EC-No. | 232-646-6 | |||
| Storage | -20°C | |||
| LGK | 10 - 13 | |||
| WGK | nwg | |||
| Specification | ||||
| Assay | approx. 70 % | |||
| Activity | min. 70 U/mg （Kunitz） | |||
（1） Ausubel, F.A., Brent, R., Kingston, R.E., Moore, D.D., Seidman, J.G., Smith, J.A. & Struhl, K. （eds.） （1995） Current Protocols in Molecular Biology. Page 3.13.1 Suppl. 8; Greene Publishing & Wiley-Interscience, New York
（2） Sambrook, J. & Russel, D.W. （2001） Molecular Cloning: A Laboratory Manual, 3rd Edition Page A4.39. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.
（3） Melton, D.A. et al. （1984） Nucleic Acids Res. 12, 7035-7056
Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing the SP6 promoter.
（4） Winter, E. et al. （1985） Proc. Natl. Acad. Sci. USA 82, 7575-7579
A method to detect and characterize point mutations in transcribed genes.
（2） Sambrook, J. & Russel, D.W. （2001） Molecular Cloning: A Laboratory Manual, 3rd Edition Page A4.39. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.
（3） Melton, D.A. et al. （1984） Nucleic Acids Res. 12, 7035-7056
Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing the SP6 promoter.
（4） Winter, E. et al. （1985） Proc. Natl. Acad. Sci. USA 82, 7575-7579
A method to detect and characterize point mutations in transcribed genes.
Ribonuclease A （RNase A） is an endoribonuclease, that specifically cleaves single-stranded RNA 3' to pyrimidine residues （cytosine, uracil）. Thereby, it generates pyrimidine-3'-phosphate or oligonucleotides with terminal pyrimidine-3'-phosphates. The pH-optimum is in the range of 7.0 - 7.5. RNase A is used for the purification of RNA-free DNA, for the removal of non-hybridized regions of RNA : DNA-hybrides or as a molecular weight marker. The enzyme is inhibited by diethyl pyrocarbonate （DEPC）, guanidinium salts （4 M GuaSCN）, β-mercaptoethanol, heavy metals, vanadyl-ribonucleoside-complexes, RNase-inhibitor from human placenta and competitively by DNA, respectively. Regarding the latter, the effect of denatured DNA is higher than by native nucleic acids. Nevertheless, RNase A is very active under very different conditions and difficult to inactivate. At low salt-concentrations （up to 100 mM NaCl）, RNase A cleaves single- and double-stranded RNA and RNA in RNA : DNA- hybrides. Under high salt concentrations （>300 mM NaCl） single-stranded RNA is cleaved only. To remove the enzyme from samples, it has to be digested by proteinase K （frequently, SDS at a final concentration of 0.6 % is added） and several phenol extractions are required. （Applications: Enzymatic manipulation of DNA and RNA: ref. 1 Suppl. 8 p. 3.13.1; minipreps of plasmid-DNA: ref. 1 Suppl. 24 p. 1.6.6; inSitu-hybridisation of cellular RNA: ref. 1 Suppl. 7 p. 14.3.8; removal of RNA from plasmid preparations: ref. 2 p. 1.51）
Stock solutions are prepared at concentrations from 1 - 10 mg/ml in 10 mM Tris · HCl, pH 7.5; 15 mM NaCl or in 10 mM Tris · HCl, pH 7.5; 1 mM EDTA, pH 8.0 （TE buffer）. The recommended working concentration is 10 μg/ml （removal of RNA from plasmid preparations; 1 hr, RT） or 100 ng/ml （preparation of "blunt ends" of double-stranded cDNA）.
Unit-definition: One unit of activity is defined as that amount of enzyme which causes the hydrolysis of RNA to yield a velocity constant, k = 1, at 25°C and pH 5.0 （Kunitz-Unit）.
Stability: RNase A aggregates during lyophilizing and storage. It has a high affinity to glas surfaces, which has to be taken into consideration. At neutral pH （e. g. in PBS pH 7.4） and high concentrations （> 10 mg/ml） the enzyme will precipitate. At +4°C （lyophilized） it is stable for several years （dry storage）, in solution （-20°C） several years or （+4°C） several weeks.
Stock solutions are prepared at concentrations from 1 - 10 mg/ml in 10 mM Tris · HCl, pH 7.5; 15 mM NaCl or in 10 mM Tris · HCl, pH 7.5; 1 mM EDTA, pH 8.0 （TE buffer）. The recommended working concentration is 10 μg/ml （removal of RNA from plasmid preparations; 1 hr, RT） or 100 ng/ml （preparation of "blunt ends" of double-stranded cDNA）.
Unit-definition: One unit of activity is defined as that amount of enzyme which causes the hydrolysis of RNA to yield a velocity constant, k = 1, at 25°C and pH 5.0 （Kunitz-Unit）.
Stability: RNase A aggregates during lyophilizing and storage. It has a high affinity to glas surfaces, which has to be taken into consideration. At neutral pH （e. g. in PBS pH 7.4） and high concentrations （> 10 mg/ml） the enzyme will precipitate. At +4°C （lyophilized） it is stable for several years （dry storage）, in solution （-20°C） several years or （+4°C） several weeks.
