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Merck

P4458

Sigma-Aldrich

Penicillin-Streptomycin

liquid, non-animal origin, suitable for cell culture, BioReagent

Synonym(e):

Pen-Strep

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About This Item

UNSPSC-Code:
12352207
NACRES:
NA.76

product name

Penicillin-Streptomycin, Solution Stabilized, with 5,000 units penicillin and 5mg streptomycin/mL, 0.1 μm filtered, BioReagent, suitable for cell culture

Qualitätsniveau

Sterilität

0.1 μm filtered

Produktlinie

BioReagent

Form

liquid

Konzentration

50 ×

Methode(n)

cell culture | mammalian: suitable

Verunreinigungen

endotoxin, tested

Wirkungsspektrum von Antibiotika

Gram-negative bacteria
Gram-positive bacteria

Wirkungsweise

cell wall synthesis | interferes
protein synthesis | interferes

Versandbedingung

dry ice

Lagertemp.

−20°C

SMILES String

CC1(C)S[C@@H]2[C@H](NC(=O)Cc3ccccc3)C(=O)N2[C@H]1C(O)=O.CNC[C@H]4[C@H](O)[C@@H](O)[C@H](CCO)O[C@H]4O[C@H]5[C@@H](O[C@@H](C)C5(O)C=O)O[C@H]6[C@H](O)[C@@H](O)[C@H](NC(N)=N)[C@@H](O)[C@@H]6NC(N)=N

InChI

1S/C23H43N7O12.C16H18N2O4S/c1-7-23(38,6-32)18(42-19-8(5-28-2)12(33)13(34)9(40-19)3-4-31)20(39-7)41-17-11(30-22(26)27)14(35)10(29-21(24)25)15(36)16(17)37;1-16(2)12(15(21)22)18-13(20)11(14(18)23-16)17-10(19)8-9-6-4-3-5-7-9/h6-20,28,31,33-38H,3-5H2,1-2H3,(H4,24,25,29)(H4,26,27,30);3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22)/t7-,8-,9-,10+,11-,12-,13-,14+,15-,16+,17+,18-,19-,20-,23+;11-,12+,14-/m01/s1

InChIKey

KMOOCZWLFBSQCW-XFOLRDBHSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

Penicillin, a β-lactam antibiotic is extremely active towards bacteria. Penicillins are also termed as penams. It is naturally occurring and has a bicyclic skeleton. Streptomycin is a pseudotrisaccharide. It comprises of a monosubstituted aminocyclitol.

Anwendung

Penicillin-Streptomycin has been used:
  • as a supplement in Dulbecco′s modified Eagle′s medium (DMEM) to maintain the Huh7 liver hepatoma cell line
  • as a supplement in Roswell park memorial institute-1640 (RPMI) medium to maintain mouse lymphoma YAC-1 cells
  • as a component in minimum essential medium Eagle to treat individual mouse spleens for the preparation of splenocytes
  • as a supplement in FMX-8 complete medium to culture Chinese hamster ovary cells

Recommended for use in cell culture media at 20 ml/L.

Biochem./physiol. Wirkung

Penicillins can prevent the synthesis of bacterial cell wall. This antibiotic can be used in the treatment of skin and urinary tract infections, upper and lower respiratory infections, and endocarditis. Streptomycin can block Mycobacterium tuberculosis in vitro. Streptomycin inhibits prokaryote protein synthesis by preventing the transition from initiation complex to chain-elongating ribosome, causing miscoding.

Komponenten

This product is formulated to contain 5,000 units penicillin and 5 mg streptomycin/mL solubilized in a proprietary citrate buffer.

Sonstige Hinweise

20ml,100ml
Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage.

Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Effect of Lactobacillus brevis KB290 on the cell-mediated cytotoxic activity of mouse splenocytes: a DNA microarray analysis
Fukui Y, et al.
The British Journal of Nutrition, 110(9), 1617-1629 (2013)
Penicillins
xPharm: The Comprehensive Pharmacology Reference (2016)
Aminoglycosides Antibiotics
Comprehensive Medicinal Chemistry II, 7, 629-652 (2007)
Streptomyces-derived quorum-sensing systems engineered for adjustable transgene expression in mammalian cells and mice
Weber W, et al.
Nucleic Acids Research, 31(14), e71-e71 (2003)
Penicillins
Comprehensive Heterocyclic Chemistry III, 2, 173-237 (2008)

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