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Merck
CN

A5147

L-氨基酸氧化酶 来源于西部菱背响尾蛇 (西部菱斑响尾蛇)

Type VI, dried venom

别名:

L-AAO, L-氨基酸:氧气 氧化还原酶(脱氨)

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化学文摘社编号:
EC 号:
MDL编号:
UNSPSC代码:
12352204
NACRES:
NA.54
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类型

Type VI

质量水平

表单

dried venom

储存温度

−20°C

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应用

L-氨基酸氧化酶可用于将L-氨基酸转化为相应的α-酮酸。 产品A5147来自Crotalus atrox。 来自Sigma的L-氨基酸氧化酶已被用于亮氨酸氨基肽酶(LAP)活性测定

生化/生理作用

L-氨基酸氧化酶参与各种代谢途径,如丙氨酸和天冬氨酸代谢,蛋氨酸代谢,缬氨酸、亮氨酸和异亮氨酸降解,酪氨酸代谢,苯丙氨酸代谢,色氨酸代谢,苯丙氨酸、酪氨酸和色氨酸生物合成以及生物碱生物合成

象形图

Skull and crossbones

警示用语:

Danger

危险声明

危险分类

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

低风险生物材料
动植物源性产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Saad Alrashdi et al.
Molecules (Basel, Switzerland), 28(1) (2023-01-09)
Indole-containing acyloins are either key intermediates of many antimicrobial/antiviral natural products or building blocks in the synthesis of biologically active molecules. As such, access to structurally diverse indole-containing acyloins has attracted considerable attention. In this report, we present a pilot
Jiro Arima et al.
The Journal of biological chemistry, 281(9), 5885-5894 (2006-01-13)
Streptomyces griseus leucine aminopeptidase (SGAP), which has two zinc atoms in its active site, is clinically important as a model for understanding the structure and mechanism of action of other metallopeptidases. SGAP is a calcium-activated and calcium-stabilized enzyme, and its
Chi-Hua Cheng et al.
Analytical biochemistry, 420(1), 93-95 (2011-09-29)
As opposed to single-cell yeast and mammalian cell lines, apoptosis has not been greatly investigated in filamentous fungi because antibodies to the relevant fungal apoptosis-related proteins are not available commercially and because multicellular organisms cannot be studied using flow cytometry.
Paola Rey-Suárez et al.
Journal of proteomics, 75(2), 655-667 (2011-10-04)
Venoms of the redtail coral snake Micrurus mipartitus from Colombia and Costa Rica were analyzed by "venomics", a proteomic strategy to determine their composition. Proteins were separated by RP-HPLC, followed by SDS-PAGE, in-gel tryptic digestion, identification by MALDI or ESI
R L Hanson et al.
Enzyme and microbial technology, 48(6-7), 445-453 (2011-11-25)
N-Cbz-4,5-dehydro-L-prolineamide or N-Boc-4,5-dehydro-L-prolineamide are alternative key intermediates for the synthesis of saxagliptin, a dipeptidyl peptidase IV (DPP4) inhibitor recently approved for treatment of type 2 diabetes mellitus. An efficient biocatalytic method was developed for conversion of L-ornithine, N-α-benzyloxycarbonyl (Cbz)-L-ornthine, and

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