17978
Amberlite™ CG-120-II
H+-form, strongly acidic, 200-400 mesh
loss
~60% loss on drying, 110 °C
particle size
200-400 mesh
Legal Information
Amberlite is a trademark of DuPont de Nemours, Inc.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Daniel Knight et al.
Antimicrobial agents and chemotherapy, 60(6), 3751-3758 (2016-04-14)
Transposon mutagenesis was used to identify novel determinants of intrinsic β-lactam resistance in Acinetobacter baumannii An EZ-Tn5 transposon insertion in a gene corresponding to the A1S_0225 sequence resulted in a 4-fold decrease in resistance to ampicillin, cefotaxime, imipenem, and ceftriaxone
Nelson C Soares et al.
Proteome science, 7, 37-37 (2009-09-30)
Acinetobacter baumannii is a nosocomial pathogen that has been associated with outbreak infections in hospitals. Despite increasing awareness about this bacterium, its proteome remains poorly characterised, however recently the complete genome of A. baumannii reference strain ATCC 17978 has been
C J Vidal et al.
Journal of chromatography, 219(1), 71-79 (1981-11-27)
Acetylcholinesterase from rat brain was solubilized with 1% (w/v) Triton X-100 and purified by affinity chromatography. Two different ligands were investigated. The most efficient purification was obtained when the enzyme was eluted from a column containing the acetylcholinesterase inhibitor N-methyl-3-aminopyridinium
Şerife Yilmaz et al.
Journal of chemotherapy (Florence, Italy), 32(6), 286-293 (2020-03-07)
Colistin resistant Acinetobacter baumannii strains are of great concern worldwide. However, the role of efflux pumps in colistin resistance needs to be elucidated. We investigated the changes in colistin MICs of 29 colistin resistant A. baumannii isolates in response to
Jiefei Wang et al.
Cell chemical biology, 26(5), 745-755 (2019-03-25)
Calprotectin (CP) inhibits bacterial viability through extracellular chelation of transition metals. However, how CP influences general metabolism remains largely unexplored. We show here that CP restricts bioavailable Zn and Fe to the pathogen Acinetobacter baumannii, inducing an extensive multi-metal perturbation
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