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Merck
CN

C8413

氯霉素乙酰转移酶 来源于大肠杆菌

buffered aqueous glycerol solution

别名:

CAT, 乙酰辅酶 A:氯霉素 3-O-乙酰转移酶

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产品名称

氯霉素乙酰转移酶 来源于大肠杆菌, buffered aqueous glycerol solution

form

buffered aqueous glycerol solution

specific activity

50,000-150,000 units/mg protein

mol wt

75 kDa (three identical subunits)

shipped in

wet ice

storage temp.

−20°C

Gene Information

Escherichia coli ... cat(2847485)

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Biochem/physiol Actions

这种酶是细菌对氯霉素产生抗性的原因。催化乙酰辅酶 A 和氯霉素转化为辅酶 A 和氯霉素 3-乙酸酯。

Other Notes

在 pH 7.8 和 25°C 下,一单位本品每分钟可以将 1.0 纳摩尔氯霉素和乙酰辅酶 A 转化为氯霉素 3-乙酸酯和辅酶 A。

Physical form

50% 甘油中的透明无色溶液,含 5mM Tris-HCl (pH 7.8) 和 0.5mM 2-巯基乙醇

Application

Chloramphenicol acetyltransferase from Escherichia coli has been used in a study to assess the construction of a novel expression system in Klebsiella pneumoniae and its application for 1,3-propanediol production. Chloramphenicol acetyltransferase from Escherichia coli has also been used in a study to investigate site-directed mutagenesis and promoter functional analysis of the RM07 DNA fragment from Halobacterium halobium.
The enzyme has been used in chloramphenicol acetyltransferase assay to optimize the transfection of plasmid DNA into primary cultures of adult mouse keratinocytes. It has also been used to assess the acetyl-CoA carboxylase-carboxyltransferase (ACC-CT) domain activity. This has been done using a coupled-two phase system measuring the selective partition of [14C]acetylchloramphenicol into an organic layer.

存储类别

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

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N A Betz et al.
In vitro cellular & developmental biology : journal of the Tissue Culture Association, 28A(3 Pt 1), 188-192 (1992-03-01)
An efficient and reproducible technique for the transfection of primary cultures of adult mouse keratinocytes has been developed. The procedure involves culturing the primary adult mouse epidermal cells at 32 degrees C in an enriched media until they reach 70
Francis Rajamohan et al.
The Journal of biological chemistry, 286(48), 41510-41519 (2011-09-29)
Inhibition of acetyl-CoA carboxylases (ACCs), a crucial enzyme for fatty acid metabolism, has been shown to promote fatty acid oxidation and reduce body fat in animal models. Therefore, ACCs are attractive targets for structure-based inhibitor design, particularly the carboxyltransferase (CT)
Yen-Ping Chen et al.
Veterinary microbiology, 154(3-4), 325-331 (2011-08-09)
The cat gene, coding for chloramphenicol acetyltransferase has been reported for conferring the chloramphenicol resistance for Riemerella anatipestifer. Chloramphenicol acetyltransferases, however, are unable to inactivate florfenicol. In this study, 66 R. anatipestifer isolates were investigated for their susceptibility to chloramphenicol
Hirofumi Nariya et al.
Applied and environmental microbiology, 77(23), 8439-8441 (2011-10-04)
A xylose-inducible gene expression vector for Clostridium perfringens was developed. Plasmid pXCH contains a chromosomal region from Clostridium difficile (xylR-P(xy)(lB)): xylR, encoding the xylose repressor, xylO, the xyl operator sequence, and P(xylB), the divergent promoter upstream of xylBA encoding xylulo
Gregory F Dolan et al.
RNA (New York, N.Y.), 20(2), 202-213 (2013-12-18)
Group I introns are ribozymes (catalytic RNAs) that excise themselves from RNA primary transcripts by catalyzing two successive transesterification reactions. These cis-splicing ribozymes can be converted into trans-splicing ribozymes, which can modify the sequence of a separate substrate RNA, both

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