Store at -20°C, avoid frequent thawing and freezing
Fluorescent DNase+RNase probe must be stored in the dark

Fluorescent DNase+RNase Probe
Detection Buffer
Nuclease-free Water
ROX Reference Dye
DNase+RNase Standard low
DNase+RNase Standard mid
DNase+RNase Standard high

DNase+RNase Detection Kit provides optimized reagents for highly sensitive, fast and easy-to-perform DNase and RNase single step detection assay. The kit allows the detection of lowest amounts of RNase A, RNase T1, RNase 1 and other RNA degrading enzymes as well as DNase I and other ss- or ds-DNA degrading enzymes. It is ideal for contamination testing of a few samples as well as for routine process monitoring.
Using the DNase+RNase Detection Kit as little as 0.2 pg RNae A and
2 munits (approx. 4 pg) of DNase I can be detected within 20-30 min.

Store at -20°C, avoid frequent thawing and freezing
Fluorescent DNase probe must be stored in the dark

Fluorescent DNase Probe
Detection Buffer
Nuclease-free Water
ROX Reference Dye
DNase Standard low
DNase Standard mid
DNase Standard high

DNase Detection Kit provides optimized reagents for a highly sensitive, fast and easy-to-perform DNase detection assay. The kit allows the detection of lowest amounts of DNase I and other ss- or ds-DNA degrading enzymes. It is the ideal tool for contamination testing of a few samples or for routine process monitoring.
Using the DNase Detection Kit as little as 2 munits (approx. 4 pg) of DNase I can be detected within 20-30 min.

store at 4°C

Substrate
Standard
Dissolving Buffer
Working Buffer I
Working Buffer II
Microtiter plate

P-CHECK^® is a trademark of PANATecs, Germany

P-CHECK^® Protease Detection Kit is based on the FRET technology (Fluorescence Resonance EnergyTransfer). This test procedure guarantees maximal sensitivity for proteases down to the picomolar range.

Store at -20°C, avoid frequent thawing and freezing

Substrate Solution
Incubation Buffer
Assay Buffer
Precipitation Reagent
Positive Control

Protease Detection Kit detects a wide variety of proteases, including serine proteases, cysteine proteases and acid proteases in biological samples. The kit is based on a labeled casein derivative as protease substrate, to be incubated with the sample for 2 to 20 hours at 37°C. Active proteases cleave the labeled casein into peptides which are measured after centrifugation in the supernatant at 492 nm.