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Merck

R1003

Sigma-Aldrich

核糖核酸酶T1 来源于米曲霉

ammonium sulfate suspension, 300,000-600,000 units/mg protein

别名:

核糖核苷-3′-脒基-寡核苷酸水解酶, 鸟粪核糖核酸酶

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About This Item

CAS号:
EC號碼:
MDL號碼:
分類程式碼代碼:
12352204
NACRES:
NA.54

生物源

Aspergillus sp. (Aspergillus oryzae)

品質等級

形狀

ammonium sulfate suspension

比活性

300,000-600,000 units/mg protein

分子量

11068 by amino acid sequence

技術

cell based assay: suitable

適合性

suitable for separating native or denatured proteins, or nucleic acids

應用

cell analysis

儲存溫度

2-8°C

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應用

来自 米曲霉的核糖核酸酶T1(RNase T1)可用于在测序之前对变性的RNA进行消化并用于蛋白折叠的研究

生化/生理作用

来自米曲霉的核糖核酸酶T1(RNase T1)是一种内切核糖核酸酶,其可在G残基后进行水解。切割发生在胍核糖核苷酸的3'-磷酸基团和相邻核苷酸的5'-羟基之间。初始产物为2':3'环磷酸核苷,其可水解成相应的3'-核苷磷酸。它与胰腺RNase的不同之处在于它可特异性攻击鸟嘌呤位点以产生具有3′-GMP末端基团的3′-GMP和寡核苷酸。

單位定義

在pH7,5,37°C条件下,一个单位可在15分钟内产生相当于 ΔA260 为 1.0 的酸可溶性寡核苷酸,反应体积为1.0 mL。底物:酵母RNA。

外觀

2.8 M (NH4)2SO4 溶液混悬液

分析報告

E1%/280法测定蛋白

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves


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Caroline Haupt et al.
Journal of the American Chemical Society, 133(29), 11154-11162 (2011-06-15)
Slow protein folding processes during which kinetic folding intermediates occur for an extended time can lead to aggregation and dysfunction in living cells. Therefore, protein folding helpers have evolved, which prevent proteins from aggregation and/or speed up folding processes. In
Elisa Bombarda et al.
The journal of physical chemistry. B, 114(5), 1994-2003 (2010-01-22)
Because of their central importance for understanding enzymatic mechanisms, pK(a) values are of great interest in biochemical research. It is common practice to determine pK(a) values of amino acid residues in proteins from NMR or FTIR titration curves by determining
Patrizia Contursi et al.
Extremophiles : life under extreme conditions, 14(5), 453-463 (2010-08-25)
The pSSVx from Sulfolobus islandicus, strain REY15/4, is a hybrid between a plasmid and a fusellovirus. A systematic study previously performed revealed the presence of nine major transcripts, the expression of which was differentially and temporally regulated over the growth
Scott Quarrier et al.
RNA (New York, N.Y.), 16(6), 1108-1117 (2010-04-24)
Structure mapping experiments (using probes such as dimethyl sulfate [DMS], kethoxal, and T1 and V1 RNases) are used to determine the secondary structures of RNA molecules. The process is iterative, combining the results of several probes with constrained minimum free-energy
Colette M Castleberry et al.
Nucleic acids research, 38(16), e162-e162 (2010-07-01)
Transfer ribonucleic acids (tRNAs) are challenging to identify and quantify from unseparated mixtures. Our lab previously developed the signature digestion approach for identifying tRNAs without specific separation. Here we describe the combination of relative quantification via enzyme-mediated isotope labeling with

商品

Instructions for working with enzymes supplied as ammonium sulfate suspensions

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