ARPENspin Omni Genomic DNA Extraction Kit

Extract high-quality DNA from diverse samples including blood, animal tissues, various microorganisms, and cultured cells

ARPENSpin Total RNA Extraction Kit

purify total RNA from samples such as blood, animal tissue, various microorganisms, and cultured cells

ARPENspin Omni Genomic DNA Extraction Kit

Fast, simple, and cost-effective way to isolate high-quality DNA.

Various samples

It uses a single protocol to extract purified DNA from various samples such as animal tissue, whole blood, buffy coat, leukocytes, bacteria, yeast, blood spots, swabs, and cultured cells.

silica-based membrane techniques

The kit employs silica-based membrane techniques in a convenient spin column, eliminating the need for expensive resins, hazardous phenol-chloroform extractions, or time-consuming alcohol precipitation.

Fast extraction in 20 minutes up to 20Kb DNA

The entire process, including lysis steps, takes less than 20 minutes. This kit can purify more than 20 kb DNA. The kit can purify DNA fragments of more than 20 kb, suitable for direct application to PCR, Southern blotting, and other enzymatic reactions.

ARPENSpin Total RNA Extraction Kit

Fast, simple, and cost-effective way to isolate high-quality RNA.

Various samples

It uses a single protocol to rapidly isolate and purify total RNA from a variety of samples like blood, animal tissues, microorganisms, cultured cells, and process multiple samples simultaneously.

silica-based membrane techniques

This kit is designed to enhance the adsorption capacity of the column membrane for RNA. The RNA is bonded to the spin column through the use of ethanol. After several rounds of washing, impurities can be effectively removed, resulting in the obtainment of high-quality total RNA with a high degree of purity.

High and pure yield of RNA

This kit can purify (OD260-OD320)/(OD280-OD320) between 1.8 -2.2, and the yield of mouse liver extraction ≥30ug/30mg suitable for various applications including Northern blotting, blotting hybridization, poly(A)+ selection, in vitro translation, RNase protect assay, RT-PCR/Real time RT-PCR analysis, and construction of cDNA library.