rna-isolation-purification-cells-primary-rat-cardiac-fibroblasts

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Get tips on using RNA Stat-60 RNA Extraction Reagent to perform RNA isolation / purification Cells - immortalized HEK 293

Products Amsbio RNA Stat-60 RNA Extraction Reagent

Get tips on using RNAGEM™ Tissue PLUS to perform RNA isolation / purification Tissue - Rat Pineal gland

Products ZyGEM RNAGEM™ Tissue PLUS

Get tips on using ExpressArt FFPE Clear RNAready to perform RNA isolation / purification Tissue - rat kidney tissue

Products Amsbio ExpressArt FFPE Clear RNAready

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 Mammalian cells Rat_Liver

Get tips on using RNAsimple Total RNA Kit to perform RNA isolation / purification Cells - immortalized H1299

Products Tiangen RNAsimple Total RNA Kit

RNA siRNA / miRNA gene silencing Rat Glial cells CCR2

RNA siRNA / miRNA gene silencing Rat Schwann cells Nrf2

RNA siRNA / miRNA gene silencing Rat Schwann cells Nrp1

RNA siRNA / miRNA gene silencing Rat Schwann cells Fyn

Microarrays enable researchers to monitor the expression of thousands of genes simultaneously. However, the sensitivity, accuracy, specificity, and reproducibility are major challenges for this technology. Cross-hybridization, combination with splice variants, is a prime source for the discrepancies in differential gene expression calls among various microarray platforms. Removing (either from production or downstream bioinformatic analysis) and/or redesigning the microarray probes prone to cross-hybridization is a reasonable strategy to increase the hybridization specificity and hence, the accuracy of the microarray measurements.

DNA Microarray RNA amplification & Labeling Rat spinal cord Hy5

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