ATP Genomic DNA Mini Kit

Introduction Format: Spin columns Sample: 1~4 ml bacterial cultures Operation: Centrifuge / vacuum manifold Operation time: 20 minutes Binding capacity: Up to 30 ?g per Column Expected yield: 25~35 ?g for high-copy plasmid;5~15 ?g per low-copy plasmid Application: DNA Library ...

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Introduction Format: Spin columns Sample: 1~4 ml bacterial cultures Operation: Centrifuge / vacuum manifold Operation time: 20 minutes Binding capacity: Up to 30 ?g per Column Expected yield: 25~35 ?g for high-copy plasmid;5~15 ?g per low-copy plasmid Application: DNA Library ...

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Quality Control The quality of ATP Gel/PCR fragments Extraction Kit is tested on a lot-to-lot basis. The efficiency of DNA recovery is tested by isolation of DNA fragment of various sizes from either aqueous solution or agarose. The purified DNA is checked by agarose gel ...

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2. ATP TM provide genomic DNA extraction protocols for smaller sample quantity. If larger sample quantity is required, user can scale up the buffer volume of the protocols proportionally. Introduction 1. ATP TM provide RBC Lysis Buffer to remove non-nucleated red blood cells ...

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The quality of ATP Genomic DNA Kit (Tissue) is tested on a lot-to-lot basis. The Kits are tested by isolation of genomic DNA from 10mg of mouse liver. The purified DNA is quantified with spectrophotometer and the yield of genomic DNA is more than 10 ...

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The quality of ATP Genomic Maxi DNA Kit (Blood/Culture Cell) is tested on a lot-to-lot basis. The Kits are tested by isolation of genomic DNA from 4 ml of human whole blood. The purified DNA is quantified with spectrophotometer and the yield of genomic DNA is > 100 ...

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The quality of ATP Genomic DNA Kit (Plant) is tested on a lot-to-lot basis. The Kits are tested by isolation of genomic DNA from 50mg young leave. The purified DNA is quantified with spectrophotometer and the yield of genomic DNA is more than 10 ...

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DNA binding, wash and elution steps can be done using a vacuum manifold or by centrifugation. 3. After washing off the contaminants, the purified DNA is eluted by a low salt elution buffer or water. 2. And then DNA in chaotropic salt is bound to the glass fiber matrix of the ...

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3. After washing off the contaminants, the purified RNA is eluted by RNase-free water. 2. And then RNA in chaotropic salt is bonded to the glass fiber matrix of the column. 1. This method uses detergents and a chaotropic salt to lyse cells and inactivate RNase. Introduction ...

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