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GALA

Sigma-Aldrich

β-半乳糖苷酶报告基因活性检测试剂盒

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About This Item

分類程式碼代碼:
12352200
NACRES:
NA.32

無菌

0.2 μm filtered

品質等級

用途

 kit sufficient for 65 tests

運輸包裝

dry ice

儲存溫度

−20°C

其他說明

The substrate used in this kit is o-nitrophenyl β-D-galactopyranoside (ONPG). ONPG generates a yellow color upon hydrolysis.

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訊號詞

Warning

危險聲明

危險分類

Skin Sens. 1

儲存類別代碼

10 - Combustible liquids

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Anna M Kielak et al.
Scientific reports, 7, 41193-41193 (2017-01-25)
Acidobacteria have been described as one of the most abundant and ubiquitous bacterial phyla in soil. However, factors contributing to this ecological success are not well elucidated mainly due to difficulties in bacterial isolation. Acidobacteria may be able to survive
V Hugouvieux et al.
Applied and environmental microbiology, 63(6), 2287-2292 (1997-06-01)
The production of endopolygalacturonase (endoPG) by Colletotrichum lindemuthianum, a fungal pathogen causing anthracnose on bean seedlings, was enhanced when the fungus was grown in liquid medium with L-arabinose or L-rhamnose as the sole carbon source. These two neutral sugars are
Shaowei Wu et al.
International journal of molecular sciences, 17(4), 511-511 (2016-04-09)
Abrus cantoniensis (Hance) is a popular Chinese vegetable consumed as a beverage, soup or folk medicine. To fully exploit the potential of the polysaccharide in Abrus cantoniensis, nine polysaccharide fractions of Abrus cantoniensis were isolated and purified (AP-AOH30-1, AP-AOH30-2, AP-AOH80-1
Claudia Massa et al.
The Biochemical journal, 407(2), 207-217 (2007-07-14)
We have recently isolated and heterologously expressed BcPeh28A, an endopolygalacturonase from the phytopathogenic Gram-negative bacterium Burkholderia cepacia. Endopolygalacturonases belong to glycoside hydrolase family 28 and are responsible for the hydrolysis of the non-esterified regions of pectins. The mode of action
J Michael O'Donnell et al.
Gene therapy, 12(12), 958-964 (2005-03-25)
While a number of virus-based delivery schemes have been developed for myocardial gene transfer, no technique has proven capable of modifying a majority of cardiac myocytes rapidly and homogeneously in the in vivo rat model, and most schemes result in

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