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Biological Data
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Biological description
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β-lactam antibiotic widely used as a selection marker for E.coli and other bacteria during plasmid DNA isolation, protein expression and gene cloning. |
Solubility & Handling
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Storage instructions
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+4°C |
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Solubility overview
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Soluble in water (100 mM) |
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Important
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This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use. |
Chemical Data
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Chemical name
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(2S,5R,6R)-6-[[(2R)-2-Amino-2-phenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid sodium salt |
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Chemical structure
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![Ampicillin sodium salt [69-52-3] Chemical Structure](data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAQAAAC1HAwCAAAAC0lEQVR4nGP6zwAAAgcBApocMXEAAAAASUVORK5CYII= "Ampicillin sodium salt [69-52-3]")
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Molecular Formula
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C16H18N3NaO4S |
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PubChem identifier
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101603128 |
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SMILES
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CC1([C@@H](N2[C@H](S1)[C@@H](C2=O)N=C([C@@H](C3=CC=CC=C3)N)[O-])C(=O)O)C.[Na+] |
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InChi
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InChI=1S/C16H19N3O4S.Na/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8;/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23);/q;+1/p-1/t9-,10-,11+,14-;/m1./s1 |
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InChiKey
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KLOHDWPABZXLGI-YWUHCJSESA-M |
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Appearance
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White to off-white |
References for Ampicillin sodium salt
References are publications that support the biological activity of the product
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Ampicillin: Rise Fall and Resurgence
Kaushik et al (2014)
J Clin Diagn Res : 8(5)
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Altering the Selection Capabilities of Common Cloning Vectors via Restriction Enzyme Mediated Gene Disruption
Manna et al (2013)
BMC Res Notes : 6(85)
Publications
These publications cite the use of Ampicillin sodium salt purchased from Hello Bio:
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Bidirectional protein-protein interactions control liquid-liquid phase separation of PSD-95 and its interaction partners
Christensen NR et al (2022)
iScience 25(2) : 103808
Antibiotic and selection marker
![Ampicillin sodium salt [69-52-3] Chemical Structure](https://m2stage-v2.hellobio.com/media/catalog/product//h/b/hb4322.png "Ampicillin sodium salt [69-52-3]")
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