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Merck

17778

Millipore

Ticarcillin Supplement

suitable for microbiology

Sinónimos:

Ticarcillin

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About This Item

Fórmula empírica (notación de Hill):
C15H16N2O6S2
Número de CAS:
Peso molecular:
384.43
EC Number:
MDL number:
UNSPSC Code:
41171614
PubChem Substance ID:
NACRES:
NA.85

agency

according to ISO 10273:2017

Quality Level

sterility

sterile

form

powder

shelf life

limited shelf life, expiry date on the label

application(s)

agriculture
environmental
food and beverages

microbiology

storage temp.

2-8°C

suitability

Yersinia spp.

SMILES string

CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](C(O)=O)c3ccsc3)C(=O)N2[C@H]1C(O)=O

InChI

1S/C15H16N2O6S2/c1-15(2)9(14(22)23)17-11(19)8(12(17)25-15)16-10(18)7(13(20)21)6-3-4-24-5-6/h3-5,7-9,12H,1-2H3,(H,16,18)(H,20,21)(H,22,23)/t7-,8-,9+,12-/m1/s1

InChI key

OHKOGUYZJXTSFX-KZFFXBSXSA-N

Application

An antibiotic supplement recommended for the selective enrichment of Yersinia enterocolitica.

Components

Composition (per vial; sufficient for 1000 mL medium): Ticarcillin 1.00 mg

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Grace A Blackwell et al.
Plasmid, 103, 36-44 (2019-04-15)
Most Acinetobacter plasmids are genus specific but their properties have not been investigated. Small plasmids with Rep_3 family replication initiation proteins and iterons are common in Acinetobacter baumannii and often carry antibiotic resistance genes and toxin-antitoxin systems. A RepAci1 plasmid
Pholawat Tingpej et al.
Respirology (Carlton, Vic.), 15(6), 923-929 (2010-06-25)
Earlier reports suggested that Pseudomonas aeruginosa frequent epidemic clones circulating in cystic fibrosis (CF) centres had increased virulence. However, recent data show no consistent associations with virulence, and suggest attenuation of virulence in chronic infection. Changes to infection control programmes
Joycelyn Ho et al.
Journal of medical microbiology, 69(3), 478-486 (2020-01-15)
Introduction.Pseudomonas syringae pv. actinidiae (Psa) has emerged as a major bacterial pathogen of kiwifruit cultivation throughout the world.Aim. We aim to introduce a CRISPR-Cas9 system, a commonly used genome editing tool, into Psa. The protocols may also be useful in
Susana Patrícia Lopes et al.
Scientific reports, 8(1), 9494-9494 (2018-06-24)
Selecting appropriate tools providing reliable quantitative measures of individual populations in biofilms is critical as we now recognize their true polymicrobial and heterogeneous nature. Here, plate count, quantitative real-time polymerase chain reaction (q-PCR) and peptide nucleic acid probe-fluorescence in situ
Cecile Formosa et al.
Nanomedicine : nanotechnology, biology, and medicine, 8(1), 12-16 (2011-10-26)
Studying living bacteria at the nanoscale in their native liquid environment opens an unexplored landscape. We focus on Pseudomonas aeruginosa and demonstrate how the cell wall is biophysically affected at the nanoscale by two reference antibiotics (ticarcillin and tobramycin). The

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