Description : The EZgeneTM 96-Well Blood DNA Kit allows rapid and reliable isolation of high-quality genomic DNA /viral DNA in a high-through-put 96-well format from a wide variety of samples including fresh, frozen, or anticoagulated whole blood, serum, plasma, bone marrow, body fluids, lymphocytes and cultured cells. Blood DNA is bound to Biomiga's ezBind matrix while proteins and other unwanted impurities are removed by two rapid wash. Pure DNA is then eluted from the matrix with Elution Buffer or ddH2O. Purified DNA is suitable for PCR, restriction digestion, and hybridization techniques. The DNA binding capacity per well is 50 µg. All components of the EZgeneTM 96-Well DNA Kit are stable for at least 12 months from date of purchase when stored at 22-25°C. Buffer BL may form precipitates in cool ambient conditions, Warm up the bottle at 37°C to dissolve before use. Store Protease K at -20°C. Buffer BL contains chaotropic salts, which may form reactive compounds when combines with bleach, Do not add bleach or acidic solutions directly to the preparation waste, ware gloves and protective eyewear when handling. Product Number GD2815-00 GD2815-01 GD2815-02 96-Well DNA Plate 1 4 20 96-Well Collection Plate (2 mL) 1 2 4 Round Well Plate (1.2 mL) 1 4 20 Caps for round-well Plate 24 x 8 96 x 8 480 x 8 Racked Microtubes 1 4 20 Caps for Racked Microtubes 12 x 8 48 x 8 240 x 8 Buffer BL 30 mL 100 mL 500 mL Protease K 50 mg 200 mg 1.0 g Buffer KB 45 mL 170 mL 820 mL DNA Wash Buffer 70 mL 280 mL 5 x 280mL Elution Buffer 40 mL 160 mL 2 x 250 mL Sealing Film 5 20 100 Instruction Booklet 1 1 1 Please read the entire manual to become familiar with the EZgeneTM 96-Well Blood DNA kit procedure. 1. Prepare a Protease K stock solution with Elution Buffer and aliquot into adequate portions. Store each aliquot at -20 °C and thaw before use. Each sample will require 25 μL of this solution. 2. Dilute DNA Wash Buffer Concentrate with absolute ethanol as follows and store at room temperature. 3. Preheat Elution Buffer at 65 °C. 4.Adjust the volume of samples to 250 μL. For samples smaller than 250 μL, add appropriate volume of PBS to 250 μL. For samples larger than 250 μL, split each sample into two 250 μL aliquots and use two wells of the 1.2 mL round well plate for lysis. Load the combined lysates into each well of the 96-Well DNA Plate. Storage of blood samples without previous treatment leads to reduced yields of genomic DNA. For the best result, blood samples should be treated as follows, The total DNA yield can be calculated as: [DNA] = (Absorbance260) x (0.05 μg/μL) x (Dilution factor) The quality of DNA can be assessed by measuring absorbance at A260/280. A ratio of (A260/A280) of 1.8-1.9 corresponds to 90%-95% purity. Introduction
Storage and Stability
Safety Inforamtion
Kit Contents
Materials to be provided by user
Before Starting
Storage of Blood Samples
Determination of Yield and Quality
- Model: GD2815-00
- Manufactured by: Biomiga