rna-isolation-purification-cells-primary-rat-brain-microvascular-endothelial-cells

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Get tips on using TRI Reagent® MRC to perform RNA isolation / purification Tissue - mouse aorta tissue

Products Molecular Research Center, Inc. TRI Reagent® MRC

Get tips on using TRI Reagent® MRC to perform RNA isolation / purification Tissue - human placental tissue

Products Molecular Research Center, Inc. TRI Reagent® MRC

Get tips on using MEBMTM Mammary Epithelial Cell Growth Basal Medium to perform 3D Cell Culture Media Mouse primary breast ephitelial cells-Mammospheres

Products Lonza MEBMTM Mammary Epithelial Cell Growth Basal Medium

Get tips on using MEBMTM Mammary Epithelial Cell Growth Basal Medium to perform 3D Cell Culture Media Human primary breast ephitelial cells-Mammospheres

Products Lonza MEBMTM Mammary Epithelial Cell Growth Basal Medium

Get tips on using PE-Cy™7 Rat Anti-Mouse TNF to perform Flow cytometry Anti-bodies Mouse - TNF-α

Products BD Biosciences PE-Cy™7 Rat Anti-Mouse TNF

Get tips on using Alexa Fluor® 488 Rat Anti-Mouse CD146 to perform Flow cytometry Anti-bodies Mouse - CD146/MCAM

Products BD Biosciences Alexa Fluor® 488 Rat Anti-Mouse CD146

RNA siRNA / miRNA gene silencing Rat Cardiomyocyte (H9C2) HIF-1α Lipid

Get tips on using Dulbecco’s Modified Eagle’s Medium/Nutrient Mixture F-12 Ham to perform Stem cell culture media NCH421K cells primary glioma

Products Sigma-Aldrich Dulbecco’s Modified Eagle’s Medium/Nutrient Mixture F-12 Ham

Site-directed mutagenesis (SDM) can be challenging, particularly during detection/confirmation of (SDM) in colonies by sequencing or PCR techniques. This common issue in SDM is heavily relying on designing of mutagenic primer pairs. The best solution is to design the mutagenic primers that have extended 3'-ends/3'-overhang. This would provide the annealing region between the mutagenic primer pair is essentially shorter. and hence ensure a lower annealing temperature for the primer pair along with a higher chance of annealing to the template.

DNA Site Directed Mutagenesis (SDM) Rat Point mutation H9C2 PP1

Site-directed mutagenesis (SDM) can be challenging, particularly during detection/confirmation of (SDM) in colonies by sequencing or PCR techniques. This common issue in SDM is heavily relying on designing of mutagenic primer pairs. The best solution is to design the mutagenic primers that have extended 3'-ends/3'-overhang. This would provide the annealing region between the mutagenic primer pair is essentially shorter. and hence ensure a lower annealing temperature for the primer pair along with a higher chance of annealing to the template.

DNA Site Directed Mutagenesis (SDM) Rat Point mutation H9C2 CELF1

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