reporter-gene-assay-luciferase-bhk-21-baby-hamster-kidney-cells

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Get tips on using Purified Hamster Anti-Mouse TCR β Chain to perform Flow cytometry Anti-bodies Mouse - TCRbeta

Products BD Biosciences Purified Hamster Anti-Mouse TCR β Chain

Get tips on using Purified NA/LE Hamster Anti-Mouse CD40 to perform Flow cytometry Anti-bodies Mouse - CD40

Products BD Biosciences Purified NA/LE Hamster Anti-Mouse CD40

Get tips on using PerCP-Cy™5.5 Hamster Anti-Mouse CD69 to perform Flow cytometry Anti-bodies Mouse - CD69

Products BD Biosciences PerCP-Cy™5.5 Hamster Anti-Mouse CD69

Get tips on using PE-Cy™7 Hamster Anti-Mouse CD11c to perform Flow cytometry Anti-bodies Mouse - CD11c

Products BD Biosciences PE-Cy™7 Hamster Anti-Mouse CD11c

Get tips on using 3D-Gene® Mouse miRNA Oligo chip (ver.21) to perform Microarray Gene expression arrays - Mouse liver tissue Cyanine-3-CTP

Products Toray 3D-Gene® Mouse miRNA Oligo chip (ver.21)

Get tips on using CelLytic™ M to perform Protein isolation Mammalian cells - BHK-21

Products Sigma-Aldrich CelLytic™ M

Get tips on using LIVE/DEAD™ Fixable Blue Dead Cell Stain Kit, for UV excitation to perform Live / Dead assay mammalian cells - BHK-21

Products Thermo Fisher Scientific LIVE/DEAD™ Fixable Blue Dead Cell Stain Kit, for UV excitation

Get tips on using TRIzol Reagent to perform RNA isolation / purification Cells - immortalized BHK-21

Products Thermo Fisher Scientific TRIzol Reagent

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) Hamster Point mutation CHO SGLT1

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) Hamster Point mutation CHO DLL1

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