Protein Expression Prokaryotic cells A. tumefaciens

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Get tips on using T-PER™ Tissue Protein Extraction Reagent to perform Protein isolation Tissue - Rabbit eye retina/choroids

Products Thermo Fisher Scientific T-PER™ Tissue Protein Extraction Reagent

Get tips on using Anti-Clara Cell Secretory Protein Antibody to perform Flow cytometry Anti-bodies Mouse - CCSP

Products Sigma-Aldrich Anti-Clara Cell Secretory Protein Antibody

Proteins Protein tag His-tag removal

DNA damage assay is a standard method for determining in-vivo/in-vitro genotoxicity by measuring the breaks in the DNA chain of animal and plant cells. Initial DNA damage leads to cell cycle arrest and, at the final stages, leads to induction of senescence or cell death (apoptosis, necrosis, autophagy, or mitotic catastrophe). Detection of DNA damage from mild to moderate to severe is challenging when studying genotoxicity in the pool of cells. It is favorable to use DNA damage assay kits available for prominent identification of the extent of damage in the analysis.

Cellular assays DNA Damage Assay A-375

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 primary vascular smooth muscle cells Biotin

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 Human endometrial stromal cells Cyanine 3-pCp

Get tips on using Mouse C Reactive Protein ELISA Kit (PTX1) (ab157712) to perform ELISA Mouse - C-Reactive Protein/CRP

Products Abcam Mouse C Reactive Protein ELISA Kit (PTX1) (ab157712)

Get tips on using UNveil Unstained Protein Ladder(10 to 200 kDa) to perform Protein Ladder Unstained

Products BIO-HELIX UNveil Unstained Protein Ladder(10 to 200 kDa)

Get tips on using Unstained Protein Standard, Broad Range (10-200 kDa) to perform Protein Ladder Unstained

Products New England BioLabs Unstained Protein Standard, Broad Range (10-200 kDa)

Get tips on using Odyssey® One-Color Protein Molecular Weight Marker to perform Protein Ladder Immunofluorescence

Products LI-COR Odyssey® One-Color Protein Molecular Weight Marker

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