DNA methylation profiling Gene specific profiling MRC-5

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Get tips on using ON-TARGETplus Human PCSK6 (5046) siRNA - Individual to perform siRNA / miRNA gene silencing Human - Detroit 562 / D562 PACE4

Products Dharmacon ON-TARGETplus Human PCSK6 (5046) siRNA - Individual

Get tips on using ON-TARGETplus Human FURIN (5045) siRNA - SMARTpool to perform siRNA / miRNA gene silencing Human - Detroit 562 / D562 Furin

Products Dharmacon ON-TARGETplus Human FURIN (5045) siRNA - SMARTpool

Get tips on using QIAshredder (250) to perform DNA fragmentation Cell lines

Products Qiagen QIAshredder (250)

Get tips on using Hoechst 33342 to perform DNA quantification Human - HeLa

Products Thermo Fisher Scientific Hoechst 33342

Protein isolation is a technique that involves isolation and/ or purification of protein from cells or tissues via chromatography or electrophoresis. The major challenges in protein isolation include: 1. The concentration of proteins in cells is variable and tends to be small for some intracellular proteins. Unlike nucleic acids, proteins cannot be amplified. 2. Proteins are more unstable than nucleic acids. They are easily denatured under suboptimal temperature, pH or salt concentrations. 3. Finally, no generalized technique/protocol can be applied for protein isolation. Proteins may have different electrostatic (number of positively or negatively charged amino acids) or hydrophobic properties. Therefore, protein purification requires multiple steps depending on their charge (a negatively charged resin/column for positively charged proteins and vice-versa), dissolution (using detergents) and unlike in the case of DNA and RNA, instead of using salts, proteins should be isolated by isoelectric precipitation.

Proteins Protein isolation Bacteria Mycobacterium smegmatis

Protein isolation is a technique that involves isolation and/ or purification of protein from cells or tissues via chromatography or electrophoresis. The major challenges in protein isolation include: 1. The concentration of proteins in cells is variable and tends to be small for some intracellular proteins. Unlike nucleic acids, proteins cannot be amplified. 2. Proteins are more unstable than nucleic acids. They are easily denatured under suboptimal temperature, pH or salt concentrations. 3. Finally, no generalized technique/protocol can be applied for protein isolation. Proteins may have different electrostatic (number of positively or negatively charged amino acids) or hydrophobic properties. Therefore, protein purification requires multiple steps depending on their charge (a negatively charged resin/column for positively charged proteins and vice-versa), dissolution (using detergents) and unlike in the case of DNA and RNA, instead of using salts, proteins should be isolated by isoelectric precipitation.

Proteins Protein isolation Bacteria Mycobacterium tuberculosis

Get tips on using QIAamp MinElute Media Kit to perform DNA isolation / purification Tissue - genital / cervical samples

Products Qiagen QIAamp MinElute Media Kit

Get tips on using CometAssay Electrophoresis Starter Kit to perform DNA Damage Assay A2780

Products Bio-Techne CometAssay Electrophoresis Starter Kit

Get tips on using CometAssay Electrophoresis System II to perform DNA Damage Assay HT1080

Products Bio-Techne CometAssay Electrophoresis System II

Get tips on using CometAssay Electrophoresis System II to perform DNA Damage Assay HeLa

Products Bio-Techne CometAssay Electrophoresis System II

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