DNA isolation / purification Bacteria Gram negative

A PCR reaction consists of the template DNA, two primers covering the amplification site, an enzyme, and buffers. However, non-specific product amplification and primer-dimer formation during set-up are major causes of PCR failure. Nevertheless, high-quality hot-start DNA polymerase and optimize reaction buffers will certainly lead to a successful PCR reaction

Get tips on using pFastBac™ Dual Expression Vector to perform Protein expression and purification Bacteria - DH10Bac™ GYS1-GN1

Get tips on using TriPure Isolation Reagent to perform RNA isolation / purification Cells - primary human preadipocytes

Get tips on using TriPure Isolation Reagent to perform RNA isolation / purification Cells - immortalized PC-12

Get tips on using TriPure Isolation Reagent to perform RNA isolation / purification Cells - immortalized RIN-5F

Get tips on using TriPure Isolation Reagent to perform RNA isolation / purification Cells - immortalized KG-1

Get tips on using TriPure Isolation Reagent to perform RNA isolation / purification Tissue - rat pancreas tissue

Get tips on using TriPure Isolation Reagent to perform RNA isolation / purification Tissue - mouse liver tissue

Get tips on using TriPure Isolation Reagent to perform RNA isolation / purification Tissue - mouse muscle tissue

Get tips on using High Pure PCR Product Purification Kit to perform DNA gel extraction / PCR product purification Product size > 15Kb