2023
DOI: 10.1016/bs.mie.2023.03.015
|View full text |Cite
|
Sign up to set email alerts
|

Kinetic characterization of methylthio-d-ribose-1-phosphate isomerase

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 21 publications
0
2
0
Order By: Relevance
“…Thirty larvae from five new replicate exposures to each compounds’ intermediate concentration of 5 mg/L were collected following an adapted methodology described by Gusso and Wiprich [ 26 ], Veeramachineni, Ubayawardhana, and Murkin [ 74 ], and Kodama, Fukui, and Kometani [ 75 ]. The larvae were collected in 200 µL of tris-citrate buffer (50 mM Tris, 2 mM EDTA, 2 mM EGTA, pH 7.4) and the samples were centrifuged at 4 °C for 10 min at 800× g .…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Thirty larvae from five new replicate exposures to each compounds’ intermediate concentration of 5 mg/L were collected following an adapted methodology described by Gusso and Wiprich [ 26 ], Veeramachineni, Ubayawardhana, and Murkin [ 74 ], and Kodama, Fukui, and Kometani [ 75 ]. The larvae were collected in 200 µL of tris-citrate buffer (50 mM Tris, 2 mM EDTA, 2 mM EGTA, pH 7.4) and the samples were centrifuged at 4 °C for 10 min at 800× g .…”
Section: Methodsmentioning
confidence: 99%
“…4.4.2. 5 ′ -Ectonucleotidase (AMP Hydrolysis) and NTPDase (ADP and ATP Hydrolysis) Activities Thirty larvae from five new replicate exposures to each compounds' intermediate concentration of 5 mg/L were collected following an adapted methodology described by Gusso and Wiprich [26], Veeramachineni, Ubayawardhana, and Murkin [74], and Kodama, Fukui, and Kometani [75]. The larvae were collected in 200 µL of tris-citrate buffer (50 mM Tris, 2 mM EDTA, 2 mM EGTA, pH 7.4) and the samples were centrifuged at 4 • C for 10 min at 800× g. The resulting supernatant was collected and subjected to a second centrifugation at 4 • C for 10 min at 21,000× g. The remaining pellets were then frozen at −80 • C, thawed, resuspended in 200 µL of tris-citrate buffer, and used for total protein quantification at 280 nm using a Power Wave XS2 microplate reader (Bio-Tek Instruments, USA).…”
Section: Biochemical Analysis 441 Ache Activitymentioning
confidence: 99%