추천 제품
재조합
expressed in E. coli
Quality Level
양식
solution
특이 활성도
≥1400 unit/μg protein
분자량
42 kDa
배송 상태
dry ice
저장 온도
−70°C
생화학적/생리학적 작용
Galactokinase catalyzes the phosphorylation of αD-galactose to produce galactose-1-phosphate as part of the Leloir pathway.
물리적 특성
N-terminal GST-tagged 42 kDa full length protein
단위 정의
One unit will convert 1.0 picomole of galactose to galactose-1-phosphate per minute at pH 7.4 at 30 °C.
물리적 형태
Supplied as a solution in 40 mM Tris-HCl, pH 8.0, 110 mM NaCl, 2.2 mM KCl, 20% glycerol, 3 mM DTT and 10-250 mM imidazole.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
P A Frey
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 10(4), 461-470 (1996-03-01)
The biological interconversion of galactose and glucose takes place only by way of the Leloir pathway and requires the three enzymes galactokinase, galactose-1-P uridylyltransferase, and UDP-galactose 4-epimerase. The only biological importance of these enzymes appears to be to provide for
Chieh Hsu et al.
Nature communications, 3, 682-682 (2012-02-23)
During evolution, genetic networks are rewired through strengthening or weakening their interactions to develop new regulatory schemes. In the galactose network, the GAL1/GAL3 paralogues and the GAL2 gene enhance their own expression mediated by the Gal4p transcriptional activator. The wiring
Sanjay K Upadhyay et al.
Journal of computer-aided molecular design, 26(7), 847-864 (2012-05-29)
The Gal4p mediated transcriptional activation of GAL genes requires the interaction between Gal3p bound with ATP and galactose and Gal80p. Though numerous studies suggest that galactose and ATP activate Gal3p/Gal1p interaction with Gal80p, neither the mechanism of activation nor the
Kajal Biswas et al.
Methods in molecular biology (Clifton, N.J.), 852, 121-131 (2012-02-14)
Recombineering is a recombination-based highly efficient method of genetic engineering. It can be used to manipulate the bacterial chromosomal DNA as well as any episomal DNA. Recombineering can be used to insert selectable or nonselectable DNA fragments and subclone DNA
Ling Lin et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(6), 1997-2002 (2012-02-07)
Promoter-specific transcriptional activators (activators) stimulate transcription through direct interactions with one or more components of the transcription machinery, termed the "target." The identification of direct in vivo targets of activators has been a major challenge. Previous studies have provided evidence
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