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	<title>antibiotics Archives - Laboratory Notes</title>
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		<title>Kanamycin A Vs Kanamycin B</title>
		<link>https://www.laboratorynotes.com/kanamycin-a-vs-kanamycin-b/</link>
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		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Wed, 04 Jun 2025 11:32:30 +0000</pubDate>
				<category><![CDATA[Lab Notes]]></category>
		<category><![CDATA[antibiotics]]></category>
		<guid isPermaLink="false">https://www.laboratorynotes.com/?p=19743</guid>

					<description><![CDATA[<p>Criteria Kanamycin A Kanamycin B Remarks Chemical Structure Composed of 2-deoxystreptamine linked to 3-amino-3-deoxy-α-D-glucopyranose and 6-amino-6-deoxy-α-D-glucopyranose Structurally similar but differs...</p>
<p>The post <a href="https://www.laboratorynotes.com/kanamycin-a-vs-kanamycin-b/">Kanamycin A Vs Kanamycin B</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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		<title>Ampicillin Trihydrate</title>
		<link>https://www.laboratorynotes.com/ampicillin-trihydrate/</link>
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		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Sun, 04 Jul 2021 13:38:15 +0000</pubDate>
				<category><![CDATA[Lab Notes]]></category>
		<category><![CDATA[Lab Notes: Microbiology]]></category>
		<category><![CDATA[ampicillin]]></category>
		<category><![CDATA[antibiotics]]></category>
		<guid isPermaLink="false">http://www.laboratorynotes.com/?p=2101</guid>

					<description><![CDATA[<p>ChemSpider ID22034 PubChem CID 23565 UNII HXQ6A1N7R6 InChIKey RXDALBZNGVATNY-CWLIKTDRSA-N CAS Number 7177-48-2 Molecular formula C16H19N3O4S.3H2O Molecular weight 403.451 g/mol Appearance...</p>
<p>The post <a href="https://www.laboratorynotes.com/ampicillin-trihydrate/">Ampicillin Trihydrate</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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		<title>Suppliers &#8211; Ampicillin Sodium salt</title>
		<link>https://www.laboratorynotes.com/suppliers-ampicillin-sodium-salt/</link>
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		<pubDate>Thu, 01 Jul 2021 10:47:49 +0000</pubDate>
				<category><![CDATA[Suppliers]]></category>
		<category><![CDATA[ampicillin]]></category>
		<category><![CDATA[antibiotics]]></category>
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					<description><![CDATA[<p>Ampicillin Sodium salt can be purchased from any of the following suppliers. You must visit the supplier’s homepage to order...</p>
<p>The post <a href="https://www.laboratorynotes.com/suppliers-ampicillin-sodium-salt/">Suppliers &#8211; Ampicillin Sodium salt</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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		<item>
		<title>β-Lactam Antibiotics</title>
		<link>https://www.laboratorynotes.com/%ce%b2-lactam-antibiotics/</link>
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		<pubDate>Wed, 30 Jun 2021 11:50:36 +0000</pubDate>
				<category><![CDATA[Lab Notes]]></category>
		<category><![CDATA[antibiotics]]></category>
		<guid isPermaLink="false">http://www.laboratorynotes.com/?p=2096</guid>

					<description><![CDATA[<p>β-Lactam antibiotics are a major class of antibiotics defined by their distinctive β-lactam ring structure. These medications have revolutionized the...</p>
<p>The post <a href="https://www.laboratorynotes.com/%ce%b2-lactam-antibiotics/">β-Lactam Antibiotics</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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		<title>Ampicillin Sodium Salt</title>
		<link>https://www.laboratorynotes.com/ampicillin-sodium-salt/</link>
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		<pubDate>Tue, 29 Jun 2021 21:08:31 +0000</pubDate>
				<category><![CDATA[Database: Chemical]]></category>
		<category><![CDATA[ampicillin]]></category>
		<category><![CDATA[antibiotics]]></category>
		<guid isPermaLink="false">http://www.laboratorynotes.com/?p=2091</guid>

					<description><![CDATA[<p>Synonym D-(−)-α-Aminobenzylpenicillin sodium saltSodium ampicillinAmpicillin sodiumAmpicillin sodium salt CAS Number 69-52-3 Beilstein Registry Number 4119211 EC Number 200-708-1 MDL number...</p>
<p>The post <a href="https://www.laboratorynotes.com/ampicillin-sodium-salt/">Ampicillin Sodium Salt</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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		<title>Ampicillin</title>
		<link>https://www.laboratorynotes.com/ampicillin/</link>
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		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Sat, 26 Jun 2021 17:05:25 +0000</pubDate>
				<category><![CDATA[Database: Chemical]]></category>
		<category><![CDATA[ampicillin]]></category>
		<category><![CDATA[antibiotics]]></category>
		<guid isPermaLink="false">http://www.laboratorynotes.com/?p=2039</guid>

					<description><![CDATA[<p>Ampicillin belongs to a group of beta-lactam antibiotics. It is classified as critically important human medicine by WHO. Ampicillin is one of the synthetic derivatives of penicillin. It was generated by adding an amino group side chain on penicillin. Ampicillin inhibits the synthesis of the bacterial cell wall by stopping the peptidoglycan cross-linking. It is effective against both gram-positive and gram-negative bacteria.  </p>
<p>The post <a href="https://www.laboratorynotes.com/ampicillin/">Ampicillin</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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		<title>Preparation of Stock Solution of Ampicillin (50 mg/ml)</title>
		<link>https://www.laboratorynotes.com/preparation-of-stock-solution-of-ampicillin-50-mg-ml/</link>
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		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Tue, 08 Sep 2020 10:50:19 +0000</pubDate>
				<category><![CDATA[Lab Notes: Microbiology]]></category>
		<category><![CDATA[Reagents]]></category>
		<category><![CDATA[Stock solution]]></category>
		<category><![CDATA[ampicillin]]></category>
		<category><![CDATA[antibiotics]]></category>
		<guid isPermaLink="false">http://www.laboratorynotes.com/?p=242</guid>

					<description><![CDATA[<p>Ampicillin is one of the most extensively used antibiotics as a selection marker in molecular biology and bacteriology. Ampicillin is available as Ampicillin anhydrous, Ampicillin trihydrate and Ampicillin sodium salt. Ampicillin sodium salt is often used to prepare stock solution as it has better solubility in water (>50 mg/ml in water). A 50 mg/ml stock solution of ampicillin can be prepared by dissolving 500 mg ampicillin sodium salt in water to a final volume of 10 ml.</p>
<p>The post <a href="https://www.laboratorynotes.com/preparation-of-stock-solution-of-ampicillin-50-mg-ml/">Preparation of Stock Solution of Ampicillin (50 mg/ml)</a> appeared first on <a href="https://www.laboratorynotes.com">Laboratory Notes</a>.</p>
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