2921 Results for: "Organic Reagents"
Wizard Plus Megapreps DNA Purification System, 5 preps, Promega®
Supplier: Promega Corporation
A simple, reliable, silica-resin-based method for rapid isolation of plasmid DNA from 1 liter cultures.
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Oligo Clean & Concentrator™, Zymo Research
Supplier: Zymo Research
Quick (2 minute) recovery of ultra-pure DNA and RNA oligonucleotides.
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Extracta Plus DNA Kits, Quantabio
Supplier: Quantabio
Rapid extraction and purification of high-quality total DNA from cultured cells or tissue.
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Maxwell HT 96 gDNA Blood Isolation System, Promega
Supplier: Promega Corporation
The Maxwell HT 96 gDNA Blood Isolation System provides a simple and reliable method for the rapid isolation of gDNA in a multiwell format. The purified gDNA can be used directly in PCR assays, microarrays and next-generation sequencing applications.
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Quick-DNA™ Fecal/Soil Microbe Kits, Zymo Research
Supplier: Zymo Research
Rapid methods for the isolation of inhibitor-free, PCR quality DNA from fecal, soil, and microbial samples in minutes including tough-to-lyse bacteria, fungi, algae, and protozoa.
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FastDNA Spin Kit for Soil, 50 ml tubes, MP Biomedicals
Supplier: MP Biomedicals
The FastDNA™-50 mL SPIN Kit for Soil is designed to efficiently isolate bacterial, fungi, plant and animal genomic DNA from soil and environmental samples.
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Nucleon PhytoPure, Cytiva
Supplier: Cytiva
Nucleon PhytoPure enables rapid chloroform extraction of high-quality, high molecular weight genomic DNA from plant and fungal samples with efficient removal of protein as well as polysaccharides.
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44-AZOPYRIDINE 2632-99-7 100MG
Supplier: Aladdin Scientific
Description4,4′-Azopyridine can be used:To prepare porous coordination polymers (PCPs) by reacting with Zn(NO3)2 and 1,4-benzenedicarboxylic acid. As a reagent for the conversion of aliphatic alcohols into disulfides under Mitsunobu conditions.
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1,2-Di(pyridin-4-yl)diazene
Supplier: Aladdin Scientific
Description4,4′-Azopyridine can be used:To prepare porous coordination polymers (PCPs) by reacting with Zn(NO3)2 and 1,4-benzenedicarboxylic acid. As a reagent for the conversion of aliphatic alcohols into disulfides under Mitsunobu conditions.
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C272939-100MG 150347-56-1 100MG
Supplier: Aladdin Scientific
Fluorescent Dye Carboxylic Acids and Their Succinimidyl EstersSuccinimidyl esters are proven to be the best reagents for amine modifications because the amide bonds that are formed are essentially identical to, and as stable as the natural peptide bonds. These reagents are generally stable and show good reactivity and selectivity with aliphatic amines. There are few factors that need be considered when SE compounds are used for conjugation reaction: 1). Solvents:For the most part, reactive dyes are hydrophobic molecules and should be dissolved in anhydrous dimethylformamide (DMF) or dimethylsulfoxide (DMSO). 2). Reaction pH: The labeling reactions of amines with succinimidyl esters are strongly pH dependent. Amine-reactive reagents react with non-protonated aliphatic amine groups, including the terminal amines of proteins and the e-amino groups of lysines. Thus amine acylation reactions are usually carried out above pH 7.5. Protein modifications by succinimidyl esters can typically be done at pH 7.5 to 8.5, whereas isothiocyanates may require a pH 9.0 to 10.0 for optimal conjugations.
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5(6)-TAMRA
Supplier: Aladdin Scientific
Fluorescent Dye Carboxylic Acids and Their Succinimidyl EstersSuccinimidyl esters are proven to be the best reagents for amine modifications because the amide bonds that are formed are essentially identical to, and as stable as the natural peptide bonds. These reagents are generally stable and show good reactivity and selectivity with aliphatic amines. There are few factors that need be considered when SE compounds are used for conjugation reaction: 1). Solvents:For the most part, reactive dyes are hydrophobic molecules and should be dissolved in anhydrous dimethylformamide (DMF) or dimethylsulfoxide (DMSO). 2). Reaction pH: The labeling reactions of amines with succinimidyl esters are strongly pH dependent. Amine-reactive reagents react with non-protonated aliphatic amine groups, including the terminal amines of proteins and the e-amino groups of lysines. Thus amine acylation reactions are usually carried out above pH 7.5. Protein modifications by succinimidyl esters can typically be done at pH 7.5 to 8.5, whereas isothiocyanates may require a pH 9.0 to 10.0 for optimal conjugations.