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Merck

S1951

Sigma-Aldrich

α-2,3-唾液酸转移酶 来源于多杀巴斯德菌

recombinant, expressed in E. coli BL21, ≥2 units/mg protein

别名:

CMP-N-乙酰神经氨酸酯:β-D-半乳糖苷α-(2,3)-N-乙酰神经氨酰转移酶

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About This Item

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

重組細胞

expressed in E. coli BL21

品質等級

形狀

lyophilized powder

比活性

≥2 units/mg protein

分子量

46.4 kDa

運輸包裝

dry ice

儲存溫度

−20°C

相关类别

一般說明

唾液酸转移酶属于糖基转移酶家族,具有催化N-乙酰神经氨酸残基转移的能力。 它是一种具有α--2,3-唾液酸转移酶活性、α-2,6-唾液酸转移酶活性、唾液酸酶活性和反式唾液酸酶活性的多功能酶。 它的分子量大小为46.4 kDa,而pI和pH分别为5.94和7.5-8.5。

生化/生理作用

唾液酸转移酶可将Neu5Ac从CMP-Neu5Ac作为一种供体底物转移至包括糖蛋白、糖脂和寡糖在内的受体分子的β-D-半乳糖基-1,4-N-乙酰基-D-氨基葡萄糖末端。
唾液酸转移酶可将Neu5Ac从CMP-Neu5Ac转移至受体分子(包括糖蛋白、糖脂和寡糖)的半乳糖基末端。

單位定義

在37 °C pH 8.0条件下,一单位将会在没分钟内催化1.0 μmol Neu-5-Ac-α-2,3LacMU从CMP-Neu-5-Ac和Lac-β−OMU的形成。

外觀

含有Tris-HCl和NaCl的冻干粉

準備報告

以0.1毫升至1毫升体积范围内的水调配冻干粉,可以得到1单位/毫升(1毫升水)至10单位/毫升(0.1毫升水)范围的浓度。

分析報告

酶活性检测是在37°C条件下含有CMP-Neu-5Ac (1 mM)以及Lac-β−OMU (1 mM) 的Tris-HCl缓冲液(100 mM, pH 8.0)中反应30 min并通过使用带有荧光检测器(325 nm 激发而372 nm 发射)的HPLC而进行的。

象形圖

Health hazard

訊號詞

Danger

危險聲明

防範說明

危險分類

Resp. Sens. 1

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Peng Zhang et al.
Bipolar disorders, 12(8), 786-792 (2010-12-24)
Multiple linkage and association studies have suggested chromosome 8q24 as a promising candidate region for bipolar disorder (BP). We performed a detailed association analysis assessing the contribution of common genetic variation in this region to the risk of BP. We
E V Chandrasekaran et al.
Journal of proteome research, 11(4), 2609-2618 (2012-02-15)
Our previous studies suggest that the α2,3sialylated T-antigen (NeuAcα2,3Galβ1,3GalNac-) and associated glycan structures are likely to be elevated during cancer. An easy and reliable strategy to label mucinous glycans that contain such carbohydrates can enable the identification of novel glycoproteins
Yoshimitsu Kakuta et al.
Glycobiology, 18(1), 66-73 (2007-10-27)
Sialyltransferases are a family of glycosyltransferases that catalyze the transfer of N-acetylneuraminic acid residues from cytidine monophosphate N-acetylneuraminic acid (CMP-NeuAc) as a donor substrate to the carbohydrate groups of glycoproteins and glycolipids as acceptor substrates. We determined the crystal structure
Sung-Wook Son et al.
Biochemical and biophysical research communications, 414(1), 159-164 (2011-09-29)
In this study we investigated for the first time the transcriptional regulation of pig Galβ1,3GalNAc α2,3-sialyltransferase (pST3Gal I) in response to TGF-β1 in porcine kidney PK-15 cells. The pST3Gal I gene was found to span about 90kb and to be
Vireak Thon et al.
Applied microbiology and biotechnology, 94(4), 977-985 (2011-11-15)
Pasteurella multocida (Pm) strain Pm70 has three putative sialyltransferase genes including Pm0188, Pm0508, and Pm1174. A Pm0188 gene homolog in Pm strain P-1059 encodes a multifunctional α2-3-sialyltransferase, PmST1, that prefers oligosaccharide acceptors. A Pm0508 gene homolog in the same strain

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Glycosyltransferases were initially considered to be specific for a single glycosyl donor and acceptor, which led to the one enzyme-one linkage concept. Subsequent observations have refuted the theory of absolute enzymatic specificity by describing the transfer of analogs of some nucleoside mono- or diphosphate sugar donors.

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